Theranostics 2019; 9(25):7826-7848. doi:10.7150/thno.37216

Review

Nanoparticle Delivery of Immunostimulatory Agents for Cancer Immunotherapy

Jia Zhuang1, Maya Holay1, Joon Ho Park1, Ronnie H. Fang1, Jie Zhang2 Corresponding address, Liangfang Zhang1 Corresponding address

1. Department of NanoEngineering, Chemical Engineering Program, and Moores Cancer Center, University of California San Diego, La Jolla, CA 92093, USA.
2. Cello Therapeutics, Inc., San Diego, CA 92121, USA.

This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
Citation:
Zhuang J, Holay M, Park JH, Fang RH, Zhang J, Zhang L. Nanoparticle Delivery of Immunostimulatory Agents for Cancer Immunotherapy. Theranostics 2019; 9(25):7826-7848. doi:10.7150/thno.37216. Available from https://www.thno.org/v09p7826.htm

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Abstract

Immunostimulatory agents, including adjuvants, cytokines, and monoclonal antibodies, hold great potential for the treatment of cancer. However, their direct administration often results in suboptimal pharmacokinetics, vulnerability to biodegradation, and compromised targeting. More recently, encapsulation into biocompatible nanoparticulate carriers has become an emerging strategy for improving the delivery of these immunotherapeutic agents. Such approaches can address many of the challenges facing current treatment modalities by endowing additional protection and significantly elevating the bioavailability of the encapsulated payloads. To further improve the delivery efficiency and subsequent immune responses associated with current nanoscale approaches, biomimetic modifications and materials have been employed to create delivery platforms with enhanced functionalities. By leveraging nature-inspired design principles, these biomimetic nanodelivery vehicles have the potential to alter the current clinical landscape of cancer immunotherapy.

Keywords: biomimetic nanoparticle, cancer immunotherapy, immune stimulation, adjuvant, cytokine, checkpoint blockade

1. Introduction

The immune system, which is composed of different subsets of specialized immune cells, is highly efficient at eliminating exogenous material. The specific recognition of foreign antigens is mediated by professional antigen-presenting cells (APCs), which can present major histocompatibility complex (MHC)-restricted epitopes to T cells in the presence of costimulatory markers to promote both cellular and humoral immune responses [1, 2]. While this process can be easily leveraged to effectively address infections caused by common pathogens, antitumor immunity is much more difficult to elicit. Although many tumor-associated antigens (TAAs) have been identified, they are generally lowly immunogenic [3]. Tumors also develop a variety of mechanisms that enable them to subvert immune attack [4, 5]. Through their ability to express immunosuppressive signaling molecules, modulate the functions of nearby immune cells, and change their phenotypes, tumor cells can escape from immune surveillance and continue to proliferate. Current cancer immunotherapies often work by rejuvenating the immune system in a manner that enables it to address the challenges associated with tumor immune escape, and many of these approaches have started to gain traction in the clinic [6]. Whether they work by unleashing the functions of T cells [7], depleting immunosuppressive immune cell populations [8], or by modulating the characteristics of the tumor microenvironment [9], the common goal shared by most modern cancer immunotherapies is to augment endogenous immunity to ultimately overcome malignant growths.

In general, the introduction of immunomodulatory compounds into the tumor microenvironment or surrounding immune-rich tissues is a promising means of elevating antitumor immunity. Here, we discuss the use of nanocarriers to enhance the delivery of these agents, which include adjuvants, secretory cytokines, and antibodies (Figure 1). Adjuvants are synthetic or naturally occurring compounds that are capable of activating pathogen recognition receptors (PRRs) found on APCs, thus generating strong proinflammatory responses [10]. They can be administered along with antigenic material to generate potent tumor-specific responses and have also been explored as monotherapies capable of nonspecifically boosting immune activity. Cytokines are employed by a broad range of immune cells for signaling and communication and can exert immunomodulatory effects in complex ways [11]. If used correctly, cytokines can directly stimulate immune effector cells at the tumor site and enhance tumor cell susceptibility to immune attack. Depending on the specific pathway being targeted, monoclonal antibodies (mAbs) can be used to antagonize immunosuppressive interactions or to promote immune stimulation [12]. While adjuvants, cytokines, and mAbs all hold significant promise as anticancer therapeutics, these compounds can still benefit greatly from the increased specificity and enhanced safety afforded by nanodelivery platforms. In particular, emerging biomimetic technologies have the potential to provide improved functionality and to significantly enhance the potency of immunotherapeutic payloads, and these platforms will be covered in detail in this review.

2. Immunostimulatory Agents

2.1 Molecular Adjuvants

A number of different adjuvants that can stimulate the immune system are being developed and tested in clinical trials [13]. One of the most popular targets for these compounds are Toll-like receptors (TLRs), which are expressed on APCs such as macrophages and dendritic cells (DCs) [14]. TLRs have evolved to recognize specific molecular patterns from foreign microorganisms that act as danger signals to the immune system [15]. TLR engagement can induce various gene expression profiles depending on the type of receptor and the type of stimuli, affecting both the innate immune response and adaptive immunity. One common target is TLR9, which can be activated by short single-stranded DNA with unmethylated CG motifs, referred to as CpG oligodeoxynucleotides (ODNs) [16]. There are three classes of CpG ODNs, each of which has different biological activities [17]. Some can be used as potent T helper cell type 1 (Th1)-biasing adjuvants and have shown great potential in cancer therapy. Another popular TLR target is TLR4, which can be activated by adjuvants such as lipopolysaccharides (LPS) [18]. Because LPS exhibits significant toxicity, a less toxic derivative, monophosphoryl lipid A (MPLA), was developed by removing a phosphate residue. As a result of this modification, MPLA exhibits 1000-fold decreased toxicity compared to LPS and has been employed in some clinically explored vaccine formulations [19-21]. Although LPS and MPLA both target TLR4, they can be associated with different cytokine secretion profiles [22].

Adjuvants that target other TLR pathways are also actively being researched. For example, poly(I:C) can activate TLR3 by mimicking viral RNAs [23]. Poly(I:C) is a synthetic double-stranded RNA that has been extensively tested against diseases such as human immunodeficiency virus, dengue, malaria, and cancer. Since RNAs are inherently susceptible to degradation by RNase, poly(I:C) has been complexed with stabilizing molecules such as polylysine to prevent enzymatic degradation [24]. Adjuvants that activate TLR5 include flagellin, which is a protein present in bacterial flagella [25]. Flagellin alone can induce tumor necrosis factor-α (TNFα) production and can elicit high antibody titers when combined with vaccine antigens. Some imidazoquinoline derivatives with antiviral properties can activate TLR7 and TLR8 by mimicking single-stranded RNAs [26]. For example, imiquimod (R837) activates TLR7 and resiquimod (R848) activates both TLR7 and TLR8, resulting in type I interferon (IFN) and interleukin-12 (IL12) production. R837 was approved by the United Stated Food and Drug Administration (FDA) and has been used in actinic keratosis [27], basal cell carcinoma [28], and genital warts [29] treatments.

Other targets for adjuvants include nucleotide-binding oligomerization domain (NOD)-like receptors and stimulator of interferon genes (STING) present on immune cells. NOD-like receptors regulate inflammation and innate immunity via inflammasomes [30]. Synthetic adjuvants such as muramyl dipeptide can activate NOD2, which leads to the production of proinflammatory cytokines such as TNFα, IL1, IL6, and IL8 [31]. STING senses cyclic dinucleotides and nucleic acids of viral or bacterial origin [32]. Activation of the STING pathway can lead to type I IFN secretion during infection [33]. Cyclic di-AMP and cyclic di-GMP are cyclic dinucleotides originating from bacteria that have been used as STING agonists in vaccine development [34]. These cyclic dinucleotides induce type I IFN and NF-κB-mediated cytokine production, helping to enhance antigen-specific T cell and humoral immune responses.

 Figure 1 

Delivery of immunotherapeutic payloads using biomimetic nanocarriers. Immunostimulatory agents such as adjuvants can be loaded along with antigenic material into biomimetic nanodelivery vehicles to enable enhanced delivery to specific immune cell subsets like antigen-presenting cells (APCs). Upon successful delivery, downstream immune processes such as T cell stimulation can be initiated to generate antitumor responses.

Theranostics Image (Click on the image to enlarge.)

2.2 Cytokines

Cytokines are proteins employed in immune signaling, and they have been widely leveraged for their immunomodulatory effects [11]. Many of the cytokines from the IFN and IL families are in clinical use or in clinical trials. IFNs are classified into three categories based on the receptors to which they bind. IFNα and IFNβ are popular examples of type I IFNs that are used as immune stimulating agents [35]. IFNα has been approved by the FDA as an adjuvant therapy for stage III melanoma. The cytokine promotes MHC class I expression, which leads to better tumor antigen recognition. In preclinical cancer models, IFNβ has shown its potential as an immunostimulatory agent, as well as its ability to suppress autoimmune reactivity. However, it has yet to be applied in the clinic due to its low bioavailability and side effects. IFNγ is the only member of the type II IFNs [36]. It promotes MHC expression in macrophages and induces the expression of costimulatory molecules on APCs. IFNγ can also promote the Th1-biased differentiation of CD4+ T cells and inhibit IL4-dependent isotype switching in B cells. Type III IFNs, which include the IFNλ group of molecules, are relatively new compared to type I or type II IFNs [37]. Although it is known that IFNλ plays a role in certain antiviral immune responses, its potential as an immunostimulatory therapeutic has yet to be fully explored.

Among the ILs, IL2 has been approved by the FDA for use in treating metastatic melanoma [38] and renal cell carcinoma [39]. IL2 promotes the activation and expansion of CD4+ and CD8+ T cells, as well as the proliferation of natural killer (NK) cells. Not only does IL2 activate immune responses, but it can also act as a mediator of immune tolerance by suppressing T cell responses [40]. Another clinically relevant IL is IL12, which acts as a growth factor for activated NK and T cells and promotes production of IFNγ [41]. IL12 can also help CD4+ T cells to differentiate into a Th1 phenotype and increases the activity of CD8+ cytotoxic T lymphocytes (CTLs). Although IL12 has gone through various preclinical investigations and showed anti-angiogenic efficacy mediated by IFNs, it has yet to be translated.

2.3 Monoclonal Antibodies

Apart from adjuvants and cytokines, mAbs represent another means of achieving immune modulation. They offer certain advantages, including high specificity, resistance against degradation in serum, and long circulation times [42]. As immunostimulatory agents, mAbs can specifically activate (agonistic mAbs) or suppress (antagonistic mAbs) certain cellular pathways, making them a compelling tool to explore [43]. Anti-CD28 can stimulate immune responses by interacting with its target, which is constitutively expressed on most resting CD4+ T cells and a significant portion of CD8+ T cells [44]. This agonistic interaction triggers signaling cascades that promote proliferation, cytokine production, anti-apoptotic gene expression, and energy metabolism. In most cases, anti-CD28 mAbs cannot work alone and their use must be accompanied by antigen-dependent T cell receptor (TCR)-mediated signals in order to properly activate T cells. 4-1BB, also known as CD137, can be found on T cells, NK cells, DCs, mast cells, and sometimes endothelial cells of metastatic tumors [45]. Use of anti-4-1BB to engage this receptor triggers signaling pathways that lead to increased expression of anti-apoptotic genes. Similar to 4-1BB, OX40 is another member of the TNF receptor superfamily, and anti-OX40 mAbs can be used to stimulate CD4+ and CD8+ T cells [46]. Activation of OX40 signaling in T cells can lead to enhanced proliferation and increased cytokine production. Another important TNF receptor is CD40, which is expressed on, but not limited to, B cells, DCs, macrophages, T cells, vascular endothelium, and some types of cancer cells [47]. CD40 ligation is crucial in the humoral immune response and anti-CD40 mAbs can be used to stimulate antitumor activity. A prominent mechanism of this antitumor activity is the activation of the antigen-presenting DC network. Lastly, glucocorticoid-induced TNF receptor (GITR) is a costimulatory molecule that is expressed on activated T cells [48]. Anti-GITR can activate GITR to increase the proliferation, activation, and cytokine production of CD4+ and CD8+ T cells.

Antagonistic mAbs can be used to downregulate or disrupt certain immune pathways that promote tumor growth [49]. Checkpoint blockade therapies based on this type of approach have experienced a significant amount of success in clinical settings [50]. PD-1, which is a member of the CD28 family, is a co-inhibitory receptor and is upregulated when CD4+ T cells, CD8+ T cells, B cells, and monocytes are activated [51]. Engagement with its ligand, referred to as PD-L1, inhibits T cell activation and proliferation, causing cell-cycle arrest but not apoptosis. The use of anti-PD-1 and anti-PD-L1 mAbs to recover CTL-mediated antitumor effects is an approach that has been widely explored in the clinic. Similarly, cytotoxic T lymphocyte-associated protein 4 (CTLA-4) is also homologous with the costimulatory receptor CD28 [52]. CTLA-4 protein expression is upregulated when T cells interact with presented versions of their cognate antigens, and this in turn leads to a decrease in T cell activation. One of the most notable mechanisms by which CTLA-4 achieves T cell inhibition is by outcompeting CD28 for ligand binding, thus decreasing costimulation. In terms of cytokines, IL10 can be a compelling target since one of its main roles is to help avoid excessive immune activation, such as in autoimmune diseases [53]. IL10 is produced by various myeloid and lymphoid cells and it suppresses macrophage and DC function, which leads to decreased activity and cytokine production. High levels of IL10 can lead to various pathologies, and IL10 antagonists have the potential to be used against chronic infection or cancer. Other novel immune checkpoint markers, including lymphocyte-activation gene 3 [54], T cell immunoglobulin- and mucin-domain-containing molecule 3 [55], T cell immunoreceptor with immunoglobulin and ITIM domains [56], V-domain immunoglobulin-containing suppressor of T cell activation [57], and B7/H3 [58], are also actively being investigated.

3. Current Delivery Strategies

3.1 Benefits of Particulate Delivery

Despite their promise as therapeutics, immunostimulatory agents usually suffer from suboptimal pharmacokinetics, vulnerability to biodegradation, and compromised cell targeting when directly administered into the body [59]. Their nonspecific interactions with proteases, nucleases, and immune cells not only reduce immunostimulatory capacity, but can often result in safety concerns and lead to excessive inflammation, toxicity, and hypersensitivity [60]. Thus, there has been high demand for methods to effectively deliver immunostimulants to their target cell populations with minimal exposure to the surrounding biological environment. Emerging delivery strategies based on nanoparticle platforms offer an effective means of addressing the underlying issue, whereby payloads are complexed with biocompatible nanomaterials [61]. The formulation of immunostimulatory payloads into nanocarriers can help to improve immune tolerance throughout the transport process, while also enhancing immune stimulation upon delivery to the appropriate immune cells.

The nanodelivery of immunostimulatory agents offers several benefits compared with use of the same compounds in their free form. First, payload entrapment and protection by a nanoparticle matrix minimizes the chance of interference caused by degradative agents and nonspecific cellular interactions [62]. This helps to prolong circulation half-life and enhances the biological stability of the payload, both of which are crucial for maximizing downstream immune stimulation. Second, owing to the relatively small size of nanocarriers, the encapsulated payloads can more readily localize and accumulate at tumor sites or immune-rich tissues via common administration routes. For example, the subcutaneous administration of nanocarriers enables efficient transport to the draining lymph nodes, where the resident immune cells can be readily manipulated [63, 64]. Furthermore, targeting capability towards specific immune cell populations can greatly enhance the efficacy of immunostimulant delivery, since most immunostimulatory agents act on specific pathways that are only relevant to certain cell subsets [65]. By leveraging proper materials design, nanoparticulate platforms can be synthesized with specific targeting functionality and controllable release to greatly improve payload bioavailability and ensure immune activation at minimal dosages of the active ingredient [66, 67]. A final advantage of nanocarriers is their ability to co-deliver immunostimulants and antigens together using the same particulate platform, which can improve the antigen presentation process and lead to better T cell stimulation [2, 68].

3.2 Current Delivery Platforms

3.2.1 Polymers

Polymeric carriers represent one of the most prevalent and well-studied immunostimulant delivery vehicles. Polymers offer a wide range of conjugation and encapsulation options, and many have excellent biocompatibility profiles that make them a safe option for immunotherapy. Additionally, nanoscale polymeric delivery systems have the inherent ability to improve cancer immunotherapy because of their tendency to accumulate in tumor sites via the enhanced permeation and retention (EPR) effect [69]. Polymeric platforms have been widely used for the delivery of adjuvant payloads. For instance, R837, along with a near-infrared dye, were co-encapsulated into a polyethylene glycol (PEG)-poly(lactic-co-glycolic acid) (PLGA) nanoparticle via an oil-in-water emulsion (Figure 2) [70]. Here, the photothermal therapy component of the platform acted not only as a means of reducing tumor cell counts, but also primed the site for immune activity by generating tumor antigens for immune cell uptake. While free adjuvants in general cannot specifically accumulate into tumors, the R837-loaded polymeric nanoparticles benefited from the EPR effect and showed preferential tumor accumulation after intravenous injection. When administered in combination with anti-CTLA-4 mAbs, which helped to reverse the immunosuppression caused by regulatory T cells, the nanoformulation greatly inhibited the growth of secondary tumors, and mice were resistant to re-challenge, proving the long-term memory effects of the treatment.

A promising immunotherapeutic approach has been to combine checkpoint inhibitor treatment together with local DC activation using adjuvants [71]. While the direct administration of adjuvants that are capable of activating DCs by triggering their PRRs have been explored, severe adverse effects and expedited clearance have limited the clinical application of this strategy [72]. To improve translational potential, nanocarriers based on a block copolymer made of methoxytriethyleneglycol methacrylate and pentafluorophenyl methacrylate have been functionalized with TLR7/8 agonists capable of locally activating DCs in the tumor site [73]. When combined with checkpoint blockades, the combination treatment was able to stall tumor growth in a B16 melanoma mouse model by eliciting DC activation and subsequent antitumor immunity. On a similar note, adjuvants can be useful agonists for the maintenance of antitumor activity after tumor resection. Because post-operation healing can often promote metastasis [74], maintaining an immunostimulatory microenvironment at the tumor site is critical.

 Figure 2 

Adjuvant delivery using polymeric nanoparticles for combination therapy. (A) Poly(lactic-co-glycolic acid) (PLGA) nanoparticles loaded with R837 and indocyanine green (ICG) can be used to generate tumor antigens and promote transition of DCs from an immature (iDC) to mature (mDC) phenotype. The antitumor effect can further be enhanced through the inclusion of checkpoint blockades such as anti-CTLA-4. (B) The nanoformulation can be used to induce drastic temperature changes at tumor sites upon irradiation. (C) Photothermal therapy together with CTLA-4 blockade delays the growth of secondary tumors. Adapted with permission from [70]. Copyright 2016 Nature Publishing Group.

Theranostics Image (Click on the image to enlarge.)

OX40 is an important TNF receptor on the surface of some activated immune cells and helps to regulate, among others, both CD4+ and CD8+ T cells [75]. Engagement of OX40 leads to proinflammatory cytokine production and T cell expansion; however, clinical trials using anti-OX40 mAbs have shown that the nonspecific nature of this immune activation makes it ineffective against lowly immunogenic tumors [76]. As a result, better antibody delivery systems capable of increasing T cell priming and immune cell exposure are of great need. In one example, anti-OX40 mAbs were attached to PLGA nanoparticles by chemical conjugation onto the surface [77]. These antibody-conjugated polymeric nanoparticles promoted increased proliferation and activation of CTLs in vitro when compared to mAbs alone, demonstrating the advantages of the nanoparticulate formulation. To add additional biological functionality, an antagonist antibody capable of blocking checkpoint inhibitors has also been conjugated onto the nanoparticle surface [78]. A combination of anti-PD-L1 and anti-OX40 were attached onto PEGylated PLGA nanoparticles via thiol-maleimide chemistry (Figure 3). With both antibodies conjugated onto the same nanoparticle surface, T cells could interact with them simultaneously, thereby increasing activation, efficacy, and memory functionalities. Improved immunotherapeutic responses compared with a free antibody mixture or single-antibody formulations were demonstrated in two murine models, highlighting the benefits of presenting both checkpoint inhibitors and immunostimulatory antibodies together on the same nanoparticle.

Acetalated dextran has recently been shown to have properties that can be used to modulate various immunological pathways, making it an good material for developing cancer immunotherapies [79]. Due to its highly tunable degradation rate, different versions of the polymer can be used to promote antigen cross-presentation through either transporter associated with antigen processing (TAP)-dependent or TAP-independent pathways. In addition to its pH-responsive and biodegradable properties, acetalated dextran is better than traditional polymer systems in its ability to efficiently load hydrophilic drugs [80]. In one study, it was shown that acetalated dextran microparticles encapsulating either CpG ODN or poly(I:C) had higher loading efficiencies and elicited stronger in vitro immune responses when compared to their PLGA counterparts [81]. Being pH-sensitive, acetalated dextran dissolves quickly under acidic conditions but remains stable at physiological conditions. This property can be taken advantage of in order to enhance adjuvant delivery to TLR receptors that reside in the acidic lysosomal compartments of APCs.

 Figure 3 

Dual delivery of antibodies for immune stimulation. (A) Anti-PD-1 and anti-OX40 mAbs can be co-delivered using a dual immunotherapy nanoparticle (DINP) design. The anti-PD-1 acts as an antagonist that reverses T cell exhaustion, while the agonistic anti-OX40 further promotes cell activation. (B) The DINP formulation improves the efficacy of combination immunotherapy in vivo . Adapted with permission from [78]. Copyright 2018 Wiley-VCH.

Theranostics Image (Click on the image to enlarge.)

3.2.2 Liposomes

Liposomes represent a popular choice for improving the biocompatibility and therapeutic lifetime of immunostimulatory agents. Payloads can be conjugated onto the liposomal membrane or loaded into the center, either directly or via an inner core material around which the liposome is coated. Recent efforts have taken advantage of liposomal carriers to deliver various immunostimulants to enhance their immune activating properties [82, 83]. A major clinical limitation of the direct use of cytokines and mAbs is their systemic toxicity, specifically on circulating lymphocytes. To overcome this challenge, nanoscale particles have been leveraged for their passive targeting capabilities to more specifically deliver these agents to tumor sites. In one recent example, PEGylated liposomes with IL2 and anti-CD137 mAbs were fabricated [84]. The immunostimulatory liposomes had remarkable tumor accumulation and improved anti-CD137 mAb and IL2 localization compared with their soluble forms. Ultimately, the formulation was successful in delaying tumor growth without adverse effects, indicating an improved safety profile.

3.2.3 Emulsions

Oil-in-water emulsions have demonstrated the ability to positively modulate immune responses, and their use as adjuvants has achieved clinical success [85]. Among other immune stimulation mechanisms, their ease of deformation allows for the lateral movement of antigens, which can enhance uptake and activation in APCs. More recent oil-in-water emulsion platforms have incorporated additional payload molecules to further improve immunotherapeutic potential. For example, polymer-squalene emulsions loaded with CpG ODN and model antigens have been used to generate antigen-specific T cell responses and promote tumor regression [77, 86, 87]. Alternatively, water-in-oil emulsions can also provide immunostimulatory properties, although the effects are generally more localized to the site of injection. In one instance, anti-CTLA-4 antagonistic mAbs and anti-CD40 agonistic mAbs were loaded into water-in-oil emulsion microparticles [88]. Due to the large size of the particles, these water-in-oil microemulsions provided a depot for localized and sustained therapeutic release when injected adjacent to the tumor site.

3.2.4 Hydrogels

Nanosized hydrogels, or nanogels, have been recognized as an excellent type of material for biomolecule delivery. They have certain advantages over other nanocarriers and are particularly well-suited for biomolecule encapsulation [89]. Nanogels can be made by the self-assembly of amphiphilic polysaccharides, and platforms based on cholesterol-bearing pullulan (CHP) have been studied for cancer immunotherapy applications [90]. In one example, CHP nanogels were shown to drain to nearby lymph nodes upon subcutaneous administration, efficiently delivering their tumor antigen payload to APCs and eliciting strong antitumor immunity [91]. Even without the co-administration of adjuvants, CHP nanogel TAA formulations have been shown to elicit both cell-based and antibody responses [92]. Other nanogel systems have also been reported for cancer immunotherapy. For instance, a bioreducible cationic alginate-polyethylenimine nanogel was used to encapsulate ovalbumin (OVA), and the resulting nanovaccine was readily taken up by DCs, which enabled presentation of the antigen to lymphocytes for eliciting both humoral and cellular immune responses [93]. To provide additional immune stimuli to nanogel systems, adjuvants can be crosslinked into the particle matrix. In an example using CpG ODN with a β-glucan nanogel, the resulting formulation induced much stronger antigen-specific Th1 responses than β-glucan nanogel alone [94]. Specifically, mice preimmunized with an adjuvanted and antigen-loaded formulation exhibited a long delay in tumor growth and improved survival after tumor inoculation.

In addition to adjuvants, cytokines can also be incorporated into nanogels. For example, recombinant murine IL12 was successfully incorporated into a CHP nanogel through simple incubation at room temperature [95]. After subcutaneous administration, the nanogel enabled the sustained release of IL12 into the bloodstream, which led to a prolonged elevation in IL12 serum levels. Repetitive administration of the formulation drastically retarded the growth of tumors without any apparent adverse effects. In another work, IL12 was encapsulated inside a modified CHP nanogel using a thiolated PEG as a crosslinker [96]. The formulation hydrolytically degraded under physiological conditions, which resulted in the prolonged release of IL12 over time. After subcutaneous administration in mice, high IL12 levels were detected in the plasma. A nanosized core-shell liposomal polymeric gel has been developed for the co-delivery of a hydrophobic drug and a hydrophilic cytokine in the same system [97]. Methacrylate-conjugated β-cyclodextrin was used to solubilize a transforming growth factor-β (TGFβ) inhibitor, and the drug-complexed β-cyclodextrin was then co-loaded inside a liposome shell along with IL2 and a biodegradable cross-linker (Figure 4). After photopolymerization, the formed hydrogel was able to deliver the two payloads into the tumor microenvironment in a sustained fashion. The release of the TGFβ inhibitor and IL2 significantly delayed tumor growth by promoting NK cell activation and CD8+ T cell infiltration in a murine B16F10 melanoma model.

3.2.5 Gold Nanoparticles

Overall, gold nanoparticles (AuNPs) are accepted as a promising delivery platform due to their relative safety and tunable nature [98]. They can also increase the potency and decrease the toxicity of immunotherapeutics due to enhanced accumulation in tumor sites via the EPR effect. In an example, AuNPs were used as substrates for multilayer coatings made by the layer-by-layer assembly of immune signals [99]. Built through electrostatic and hydrophobic interactions, this polyelectrolyte self-assembled formulation contained poly(I:C) adjuvant and peptide antigens. Similar to other nanovaccine platforms, the co-delivery of adjuvant and antigen acted synergistically to provide greater expansion of CD8+ T cells when compared to immunization with a simple mixture of the components. The AuNP core also provided an appropriately sized substrate to aid in efficient uptake by APCs. The introduction of active targeting moieties can further improve potency and safety, offering the opportunity for active cytokine delivery without systemic toxicity. For example, AuNPs conjugated with a tumor homing peptide that recognizes and binds to CD13 on tumor endothelium were shown to effectively carry and release TNFTheranostics inline graphic in vivo [100]. Notably, administration of free cytokine at the same dosage showed no activity, highlighting the benefits of nanodelivery.

AuNPs may provide additional functionalities to antibody-based cancer immunotherapy, particularly given their ability to be used as contrast agents for computed tomography (CT) imaging and as transducers for photothermal therapy. When conjugated with checkpoint inhibitors, AuNPs can be made into theranostic platforms. In one example, anti-PD-L1-conjugated AuNPs were administered to tumor-bearing mice [101]. When the mice underwent a CT scan, the signal correlated well with tumor growth and T cell infiltration, providing evidence that the formulations could be effectively used to predict treatment outcomes. In addition to CT imaging, AuNPs also exhibit surface plasmon resonance in the near-infrared range, thus enabling their use for photothermal therapy in combination with chemoimmunotherapy [102].

 Figure 4 

Dual delivery of immunostimulatory payloads using liposomal polymeric nanogels. (A) IL2 and a TGFβ inhibitor, SB505, complexed with cyclodextrin (CD) are loaded inside a biodegradable polymer hydrogel and coated with liposomal material to form a nanolipogel (nLG). (B) The dual-loaded nLG formulation enables significant control of tumor growth and extends survival in a cancer model. Adapted with permission from [97]. Copyright 2012 Nature Publishing Group.

Theranostics Image (Click on the image to enlarge.)

3.2.6 Mesoporous Silica

Mesoporous silica nanoparticles (MSNs) have been studied in the field of nanomedicine. Unlike conventional aluminum adjuvants, MSNs can be easily doped with components that can improve their biodegradability and biocompatibility profiles [103, 104]. Owing to the intrinsic high payload encapsulation capacity afforded by their porous structures, MSNs can act as delivery vehicles for a variety of immunostimulatory agents. In the case of adjuvants, combination therapies based on MSNs appear to be an effective approach. In one example, liposome-coated MSNs were loaded with doxorubicin and oxaliplatin as apoptosis inducers along with indoximod, an immunometabolic adjuvant that can interfere with immunosuppressive pathways in the tumor microenvironment [105]. These particles benefited from increased circulation half-life and passive tumor targeting due to their biocompatible nature and nanoscale size. In a luciferase-expressing orthotropic pancreatic cancer model, tumor growth was significantly controlled with this combination therapy, and antigen-specific CTLs were clearly present.

MSNs may also provide a platform for reducing the systemic toxicity of encapsulated payloads, a necessity for the clinical use of many cytokines. For instance, the biologically active dosage of TNFTheranostics inline graphic is one order of magnitude higher than the maximal permitted dosage for intravenous administration [106]. To overcome this hurdle, MSNs can be functionalized to shield and control TNFTheranostics inline graphic delivery. In an example, MSNs were fabricated with a pH-sensitive copolymer that acted as a gatekeeper [107]. This platform enabled high drug loading in the mesopores of the MSNs and localized release, which was facilitated by the acid-triggered degradation of the copolymer. It has also been shown that mesoporous silica itself can act as a costimulant, provoking Th1 immunity and inducing both primary and memory immune responses [108]. Its adjuvancy is heavily dependent on size and porosity. While maintaining high loading capacity and biocompatibility, large-pore MSNs capable of inducing strong immune responses when combined with photothermal agents and model antigens have been fabricated [109]. Importantly, when compared directly to their silica counterparts, the MSNs generated a higher frequency of CD4+ and CD8+ T cells, highlighting the adjuvanting properties of particles. In a final example of MSN usage, biodegradable glutathione-depleted dendritic mesoporous organosilica nanoparticles were loaded with a model antigen and CpG ODN [110]. Here, not only were the MSNs able to deliver their contents intracellularly, but they were also used to neutralize intracellular glutathione, leading to an excess generation of reactive oxygen species that served to further intensify immune responses.

4. Biomimetic Delivery Strategies

4.1 Introduction to Biomimetic Delivery

Particulate delivery systems have demonstrated the ability to enhance the bioavailability of immunostimulants and can promote increased immune activation; however, conventional platforms can still be limited by certain pitfalls. For instance, in spite of effective incorporation into delivery systems, some of these immunostimulatory agents still need to be delivered in large quantities to achieve the desired effects, which necessitates the use of delivery platforms with high loading yields [111]. Finding alternative solutions to achieve better immune stimulation at lower dosages would thus be highly beneficial. Another challenge with many conventional delivery platforms is that they are still regarded as foreign by the immune system, which can lead to rapid immune clearance or unwanted immune responses [112]. Furthermore, delivery of immunostimulant payloads to the appropriate immune cell populations is essential for proper immune activation. As such, targeted delivery approaches could ensure better immune recognition and augment overall immune responses [113].

An ideal immunostimulant delivery platform would interact minimally with irrelevant cells but elicit strong immune stimulation upon reaching target immune cells [114]. As a result, on-demand immune activation could be achieved without compromised safety or tolerability parameters. Recently, biomimetic nanodelivery platforms have been increasingly employed for the delivery of immunostimulatory agents because of their ability to readily fulfill some of these design requirements [115-118]. Biomimetic modifications or delivery vehicles have the potential to significantly improve upon the overall delivery efficiency and subsequent immune responses associated with current delivery platforms. In this section, three general approaches for achieving biomimetic delivery will be discussed in depth (Table 1).

4.2 Biomimetic Modifications

Biological targeting functionality can be achieved by employing naturally occurring moieties to modify the surface of nanoparticles, thus enhancing uptake efficiency by target immune cells. These modifications are oftentimes achieved through chemical conjugation or physical incorporation processes that are easy to implement and highly controllable [66]. One representative ligand is mannose, which has affinity to receptors that are abundant on APCs [119]. Mannose receptors on macrophages and DCs enhance affinity towards the cell surface of microorganisms, facilitating their uptake and subsequent presentation to T cells [120]. When mannose is attached as a targeting ligand to immunostimulant delivery platforms, these mannosylated vehicles can be readily recognized and internalized by APCs, resulting in enhanced immune stimulation. In one example, a vaccine delivery system based on mannosylated chitosan microspheres was formulated for intranasal mucosal vaccination [121]. Compared to unmodified particles, the mannosylated microspheres could tightly bind with mannose receptors on murine macrophages and stimulated immunoglobulin production. Similarly, a PEG-sheddable, mannose-modified polymeric nanoparticle platform has been assembled and shown to efficiently target tumor-associated macrophages after PEG shedding in the acidic tumor microenvironment [122]. In a case of DC targeting, mannose was used to modify lipid-calcium phosphate nanoparticles, which contained the Trp2 melanoma self-antigen and CpG ODN as an adjuvant for immunotherapy against melanoma [123, 124].

Mannosylation can help to enhance nanoparticle localization in the lymph nodes, facilitating antigen presentation by DCs. In an example, mannose was selected to decorate chitosan nanoparticles [125]. Due to the innate immunostimulatory effect of chitosan, the nanoparticles were able to elicit strong immune responses without the addition of any other immunostimulants. The mannose-modified chitosan nanoparticles were loaded with whole tumor cell lysate prepared from B16 melanoma cells. Prompt uptake by endogenous DCs within the draining lymph node was observed, which correlated with an elevation in IFNγ and IL4 levels. The therapeutic effects of this formulation were remarkable and resulted in a significant delay of tumor growth in an animal model of melanoma.

DC targeting can also be achieved using other sugar monomers, and galactose modification is another example of biomimetic targeting using simple sugar ligands. Galactosylation was performed on dextran-retinal nanogels for cancer vaccine delivery [126]. The formulation exhibited improved cell targeting, which translated to significantly improved DC maturation. With its inherent adjuvancy, this immunostimulatory nanogel platform represented a potent delivery system for anticancer vaccination. Additionally, more complex carbohydrates have been studied for their natural binding interactions with immune cells. Among these, glycans have been employed as biomimetic targeting moieties. Lewis-type (Le) glycan structures can be grafted to delivery vehicles for specific binding to DC-specific intercellular adhesion molecule-3-grabbing nonintegrin (DC-SIGN) expressed on DCs [127]. In one example, liposomes were modified with targeting glycans LeB or LeX, which result in increased binding and internalization by bone marrow-derived DCs expressing DC-SIGN [128]. This glycoliposome-based vaccine could boost CD4+ and CD8+ T cell responses when the melanoma antigen MART1 was co-delivered.

4.3 Natural Carriers

Leveraging natural constructs for biomolecule transportation is another strategy for delivering immunostimulatory agents. By deriving nanovehicles from biological systems and loading them with immunostimulants, these delivery platforms can induce potent immune responses by targeting and interacting with specific immune cell subtypes. Additionally, because many of these carriers are either naturally occurring or easily self-assembled, their production can be readily streamlined, which enhances their translational potential.

 Table 1 

Biomimetic strategies for the nanodelivery of immunostimulatory agents.

StrategyKey pointsExamples
Biomimetic modifications
  • Direct modification of traditional nanocarriers.
  • Facile and controllable processes.
Simple sugars[123, 124, 126]
Glycans[128]
Natural carriers
  • Adaptation of natural carriers from biological systems.
  • Straightforward collection, derivation, or self-assembly.
  • Natural immune stimulation or targeting properties.
  • High biocompatibility.
Virus nanoparticles[133, 137, 138]
Protein nanoparticles[148, 150, 153, 157, 159]
Oligonucleotides/polypeptides[169-173]
Lipoproteins[163-165]
Cell membrane vesicles [176-178, 180, 184]
Genetically modified vesicles[187, 189, 193, 194]
Cell membrane hybrids
  • Combination of naturally occurring and synthetic nanomaterials.
  • Natural immune stimulation or targeting properties.
  • Multimodal functionality.
White blood cell hybrids[200, 202, 203]
Red blood cell hybrids[208-210]
Cancer cell hybrids[216, 217, 219-221]

4.3.1 Virus Nanoparticles

Among the naturally occurring nanocarriers, virus-like particles (VLPs) have attracted significant attention, as they can be readily used to induce immune responses. VLPs are protein structures isolated from viruses that can inherit viral targeting capabilities and lack the presence of potentially dangerous genetic material [129]. Viruses can inherently activate immune responses through repetitive surface structures and pathogen-associated molecular patterns, which often carry over to VLPs [130]. Identified as exogenous, VLPs can trigger potent immunity on their own, which can greatly reduce the need for incorporating other immunostimulants. Thus, owing to their intrinsic targeting and immunogenicity, VLPs can promote better antigen delivery, boost immune responses, and enhance antigen presentation to the adaptive immune system [131].

A notable example of a VLP platform for immunomodulation is one based on the cowpea mosaic virus (CPMV), which has been shown to interact with APCs [132]. In one such work, VLPs made from CPMV (CPMV-VLPs) suppressed established metastatic B16F10 melanoma and generated potent systemic antitumor immunity against the poorly immunogenic cancer cells [133]. After intratracheal administration, CPMV-VLPs activated neutrophils in the tumor microenvironment and coordinated downstream antitumor immune responses. In combination with an antigenic peptide derived from the human epidermal growth factor receptor 2 (HER2) protein, CPMV-VLPs have also served as a cancer vaccine for the treatment of HER2+ tumors [134]. Upon in vivo administration, the CPMV-VLP platform shows significant lymph node accumulation and potently activates APCs [135].

Rod-shaped plant viruses such as the tobacco mosaic virus (TMV) have also been investigated. For example, vaccination using antigen-carrying TMV-VLPs has demonstrated efficacy against various tumor models [136]. TMV-VLPs have been found to participate in specific interactions with DCs and lymphocytes and can effectively stimulate APC activation. VLP systems based on the bacteriophage Qβ have demonstrated the ability to promote DC maturation and CTL stimulation [137]. CpG ODN was loaded into Qβ-VLPs for synergistic immune activation, and the resulting formulation was shown to potently prime CTL responses and maintain memory CTL levels. Additionally, a lentivector has been engineered for specific targeting to DCs [138]. The platform employed a viral glycoprotein from the Sindbis virus, enabling it to avidly bind with the DC surface protein DC-SIGN and induce cell maturation. Using OVA as a model antigen, the engineered lentivector promoted production of a high frequency of OVA-specific CD8+ T cells after subcutaneous administration in a murine model. VLPs derived from other virus sources, such as human papillomavirus [139, 140], enterovirus 71 [141, 142], and hepatitis B [143, 144], have also been evaluated for cancer immunotherapy applications.

4.3.2 Protein Nanoparticles

Protein-based nanoparticles can be obtained by the self-assembly of protein structures from sources other than viruses [145]. These particles exhibit highly-ordered surface patterns and geometries, which make them competitive delivery platforms for cancer immunotherapy applications [146]. Nanoparticles assembled from the E2 component of pyruvate dehydrogenase have become an emerging class of nanocarriers for biomimetic delivery [147]. Because of their small size, E2 nanoparticles are well-suited for lymphatic transport and DC uptake. Systematic work on the utilization of E2 nanoparticles as biomimetic carriers for cancer immunotherapy have been published. In one work, a virus-mimicking DC-targeted vaccine platform was engineered to deliver the DC-activating CpG ODN (Figure 5) [148]. By co-delivering a peptide epitope from OVA along with the adjuvant using the E2 nanoparticle, DC maturation and antigen cross-presentation were achieved after particle uptake by DCs. Impressively, CpG ODN in the E2 formulation could activate DCs at a 25-fold lower concentration than free CpG ODN, which highlights the high delivery efficiency of this approach. Ultimately, the formulation was able to increase and prolong antigen-specific CD8+ T cell activation. In subsequent works, a variety of TAAs have been successfully delivered together with CpG ODN using E2 nanoparticles for cancer vaccination [149, 150].

Heat-shock proteins (HSPs) have also been explored for use in nanoformulations for cancer immunotherapy [151]. Protein nanoparticles derived from HSPs can exhibit strong receptor-specific interactions with APCs, which facilitates downstream antigen presentation and immune stimulation [152]. Several in vivo studies have been conducted on the use of HSP nanoparticles for immunization applications. For example, antigenic peptides bound to HSP96 have been used as cancer vaccines for patients with recurrent glioblastoma multiforme and colorectal liver metastases [153, 154]. Similarly, immunization with natural HSP110 complexed with the melanoma-associated antigen gp100 protected mice against subsequent challenge with gp100-expressing B16 melanoma by bolstering both CD4+ and CD8+ T cell populations [155].

Other protein nanoparticles that have been used as natural carriers for antigen delivery include ferritin and protein vault nanoparticles. Other than their applications in drug delivery and imaging, ferritin nanoparticles were recently studied for cancer immunotherapy [156]. Antigenic peptides derived from OVA were introduced to ferritin nanoparticles via attachment onto the exterior surface or encapsulation inside the interior cavity [157]. Immunization with the antigen-loaded ferritin nanoparticles could efficiently induce antigen-specific CD4+ and CD8+ T cell proliferation in mice. Similarly, the inner cavity of vault nanoparticles can be used to encapsulate payloads, including immunostimulatory agents [158]. For example, they were used to efficiently deliver CCL21, a lymphoid chemokine predominantly expressed in lymph nodes, in order to promote antitumor activity and inhibit lung cancer growth in vivo [159]. Intratumoral administration of the CCL21-complexed formulation enhanced CCL21-associated leukocytic infiltrates and reduced the frequency of immunosuppressive cells.

4.3.3 Lipoproteins

Another popular type of biomimetic material that can be used for immunotherapeutic applications is lipoproteins, which are endogenous nanocarriers involved in the metabolic transport of fat molecules, as well as biomolecules such proteins, vitamins, hormones, and miRNA [160]. Due to their high biocompatibility and long lifespan, lipoprotein-based nanocarriers have become emerging delivery vehicles for exogenous payload transport [161]. Furthermore, the size of lipoproteins can be tuned for efficient lymph node draining and promotion of adaptive immune responses [162]. Synthetic high-density lipoprotein (sHDL)-mimicking nanodiscs for personalized neoantigen vaccination and cancer immunotherapy have recently been reported (Figure 6) [163]. In the design, cholesterol-modified CpG ODN and identified neoantigen peptides were added to the sHDL nanodiscs to prepare homogeneous ultrasmall cancer nanovaccines. The sHDL nanodiscs improved delivery to lymphoid organs and stimulated antigen presentation by DCs. Remarkably, the nanodiscs elicited a more than 30-fold greater frequency of antigen-specific CTLs compared with a soluble CpG ODN formulation, validating the robustness of using sHDL as an immunostimulant delivery platform. When combined with other immunotherapies such as anti-PD-L1 or anti-CTLA-4 mAbs, the sHDL nanodiscs could eradicate established MC-38 and B16F10 tumors in vivo .

 Figure 5 

Adjuvant and antigen delivery using protein-based nanoparticles. (A) CpG ODN and a peptide antigen can be encapsulated into E2 protein nanoparticles for use as an anticancer vaccine formulation. Upon delivery into immature DCs (iDCs), they can promote transition into a mature phenotype (mDC) and enhance antigen cross-presentation to T cells. (B) The CpG-loaded E2 protein nanoparticles enhance dendritic cell maturation. Adapted with permission from [148]. Copyright 2013 American Chemical Society.

Theranostics Image (Click on the image to enlarge.)
 Figure 6 

Adjuvant and antigen delivery using lipoprotein nanoparticles. (A) Synthetic high-density lipoprotein (sHDL) nanodiscs can be inserted with antigens (Ag) and adjuvants (CpG) using a cysteine-serine-serine (CSS) linker and cholesterol (Cho), respectively. Upon administration, the nanoparticles can drain into nearby lymph nodes, where they are uptaken by DCs that can subsequently activate tumor-specific T cell populations. (B) The dual-loaded nanodisc formulation elicits strong antigen-specific T cell responses and greatly inhibits tumor growth. Adapted with permission from [163]. Copyright 2017 Nature Publishing Group.

Theranostics Image (Click on the image to enlarge.)

Furthermore, other TLR agonists such as MPLA have been successfully incorporated into nanolipoproteins via self-assembly [164]. Compared to administration of the agonist alone, its immunostimulatory profile could be significantly enhanced in the nanoformulation, resulting in elevated cytokine levels and upregulation of immunoregulatory genes. In another work, MPLA and CpG ODN were readily loaded into Ni2+-chelating nanodiscs via insertion into loosely packed lipid bilayers [165]. His-tagged antigens were then loaded into the nanodiscs via binding to Ni2+. It is noteworthy that the adjuvant dosages in the nanodisc formulations were 10-fold lower than what was needed to elicit similar antibody levels and immune responses by independent administration of the components. Overall, lipoprotein-based nanocarriers represent an effective platform for antigen and adjuvant co-delivery. Additionally, it has been shown that co-delivery of chemotherapeutics along with immunostimulatory payloads via these platforms can help to further amplify antitumor efficacy [166, 167].

4.3.4 Oligonucleotides and Polypeptides

Oligonucleotides can be designed to self-assemble into nanoparticles with well-defined structures and uniform sizes, and these particles have been leveraged for the delivery of immunostimulatory agents [168]. In particular, CpG ODNs have been attached to structural oligonucleotides and assembled into multivalent DNA nanostructures [169]. These particles were readily taken up by APCs and engaged TLR9 to activate proinflammatory immune processes. In another approach, flower-like nanostructures were self-assembled from long nucleotides integrated with tandem CpG ODNs through rolling circle replication [170]. These DNA nanoparticles were able to efficiently deliver the CpG payload while preventing it from nuclease degradation. CpG-containing oligonucleotide nanostructures can also be used for the co-delivery of additional payloads. In one of such example, a programmable DNA nanocomplex was constructed through the self-assembly of a model antigen streptavidin and CpG ODN with precise control over valency and spatial arrangement [171]. The resulting antigen-adjuvant nanocomplex could be used to induce long-lasting antigen-specific immunity. In another work, anti-PD-1 mAbs were loaded into a CpG ODN nanostructure to achieve synergistic action while reducing potential side effects [172]. Similar to oligonucleotide nanoparticles, those based on polypeptides have also been tested for the delivery of immunostimulatory payloads. In one representative work, CpG ODN was conjugated onto polyglutamic acid, and microparticles were obtained through infiltration of the conjugates into porous silica templates, followed by crosslinking of the polypeptide chains and subsequent template removal [173]. The formulation was used to successfully deliver CpG ODN to primary human DCs.

4.3.5 Cell Membrane Vesicles

The last major class of naturally occurring delivery vehicles is cell membrane vesicles. Payload delivery using cell-derived membrane vesicles enables concurrent use of multiple membrane biomolecules and biomarkers for functions such as immune cell targeting, cytosolic localization, and elicitation of cytokine production, among others [115]. Exosomes are fragmented vesicles secreted from cells and have essential roles in cellular signaling and metabolic transport [174]. Depending on their origin, they can exhibit natural affinity towards specific tissues within the body. In the presence of proper immune stimulation, tumor cell-derived exosomes containing TAAs can induce strong adaptive immunity when delivered to APCs [175]. For instance, CpG ODN was incorporated onto exosomes derived from modified B16BL6 cells [176]. The CpG ODN-carrying exosomes were effective at inducing maturation of DCs for enhanced TAA presentation and generation of B16BL6-specific CTLs. Immunization with the modified exosome vaccine resulted in stronger in vivo immunotherapeutic efficacy on B16BL6-challenged mice compared with the co-administration of exosomes and CpG ODN. Tumor membrane has also been utilized for antigen inclusion and adjuvant delivery in a different type of approach [177]. In the example, OVA-expressing B16F10 melanoma cells were lysed and vesiculated by sonication. Lipid-conjugated PEG and cholesterol-linked CpG ODN were then loaded onto the nanoparticles via lipid insertion. The resulting tumor membrane vesicle-based formulation exhibited effective lymph node draining and induced the generation of OVA-specific CTLs. When combined with anti-PD-L1 immunotherapy, the treatment mediated complete tumor regression in more than half of the animals that were treated and protected all survivors against a subsequent tumor cell re-challenge. Adjuvant loading can also be achieved by incorporation into tumor membrane particles both before and after vesiculation. In an example, whole B16F10 melanoma cells were broken down into membrane-enclosed vesicular compartments by extrusion or sonication in the presence of CpG ODN, followed by incubation with MPLA [178]. The breadth and diversity of the TAA repertoire was maintained on these membrane particles. The formulation promoted the uptake of the loaded adjuvant payloads and potentiated DC activation. When administered in vivo, the adjuvant-loaded particles stimulated antigen-specific cellular and humoral immune responses against B16F10.

Unlike membrane vesicles from tumor origins, those derived from innate immune cells can be directly leveraged for downstream immune stimulation. For instance, membrane vesicles derived from DCs primed with tumor vesicles have been shown to activate T cells and promote robust antitumor immunity [179]. In another example, immature DCs separated from C57BL/6 mice were pretreated and stimulated by the TLR4 agonist MPLA, which led to the elevated expression of costimulatory markers [180]. DC membrane vesicles were then obtained after multiple freeze-thaw cycles. A model antigenic peptide from OVA was loaded into the membrane vesicles, and the resulting formulation was shown to activate immature DCs in situ and augment the expansion of antigen-specific CD8+ T cells.

Bacterial outer membrane vesicles (OMVs) have also been explored for cancer immunotherapy applications. OMVs are lipid vesicles released from the outer membrane of Gram-negative bacteria and serve a variety of roles during infection [181]. They contain a number of natural adjuvants such as LPS, flagellin, and peptidoglycan that can be used to trigger strong immune reactions [182]. This intrinsic immunostimulatory property has been tested in different disease applications [183]. The potential of Escherichia coli OMVs as an effective anticancer agent has been explored, where they were tested against four different tumor models (CT26, MC38, B16BL6, and 4T1) [184]. Intravenous administration of the OMVs led to accumulation in tumor tissue and induced cytokine production that enabled the growth of established tumors to be controlled.

4.3.6 Genetically Modified Membrane Vesicles

In addition to their ability to encapsulate and deliver immunotherapeutic payloads, natural membrane vesicles can be genetically modified to introduce additional functionalities. IL12 plays an important role in the activation of NK cells and CTLs [185]. However, the direct administration of IL12 can cause severe adverse effects, which undermine its benefits in cancer immunotherapy applications [186]. In one work, cells were genetically modified to express functional IL12 using a glycolipid anchor [187]. The anchored IL12 could then be efficiently intercalated and transferred onto membrane vesicles isolated from various tumor cell lines. It was found that the incorporation of IL12 onto the tumor membrane vesicles could significantly induce T cell proliferation and the release of IFNγ. In a subsequent work, together with IL12, glycolipid-anchored HER2 and CD80 were also transferred to plasma membrane vesicles homogenized from tumor tissues [188]. The IL12 and CD80 served to enhance immune stimulation against the HER2 antigen. Immunization with these vesicles induced strong HER2-specific immune responses and resulted in complete protection against HER2+ tumor challenge.

In another type of approach, the engineering of membrane vesicles to express immunoregulatory proteins can be used to achieve a checkpoint blockade effect for antitumor therapy. In one work, PD-1 was stably expressed on the membrane of HEK 293T cells, which were subsequently extruded to form nanovesicles [189]. The resulting PD-1-presenting membrane vesicles could effectively bind to and neutralize the PD-L1 ligand on tumor cells, leading to the reactivation of exhausted antigen-specific CD8+ T cells. Furthermore, using a similar editing process, PD-1 receptors were expressed on megakaryocytes before differentiation into platelets [190]. Taking advantage of the outstanding tumor targeting ability of platelets, the platelet-derived PD-1-containing membrane vesicles could be retained at the tumor site post-resection to enhance the activity of CD8+ T cells against residual disease.

Other protein ligands can be integrated into membrane vesicles using similar genetic modification approaches. A virus-mimetic nanovesicle was produced by expressing viral proteins in mammalian cells, which were then sonicated in the presence of surfactants [191]. This approach enabled the display of functional polypeptides with correct conformations and could aid in future vaccine design. In a different type of example, a hepatitis B virus receptor was engineered into nanovesicles in order to generate nanoscale decoys that could block infection by the virus in vivo [192]. Besides viral proteins, tumor-targeting moieties, such as human epidermal growth factor or anti-HER2 affibodies, have been successfully integrated onto nanovesicles [193]. The engineered liposome-like nanovesicles could be used to enhance the delivery of phototheranostic or chemotherapeutic agents to tumor cells.

In terms of bacterial vesicles, OMVs can also be easily modified to introduce additional functional components. As an example, E. coli OMVs were genetically decorated with two epitopes present in B16F10 melanoma cells expressing epidermal growth factor receptor variant III, and the resulting formulation was tested for its protective activity against tumor growth [194]. High levels of antigen-specific antibody titers were elicited, and significant amounts of tumor-infiltrating lymphocytes were found at the tumor site. This ultimately led to effective protection of the immunized mice upon tumor challenge.

4.4 Engineered Cell Membrane Hybrids

For payload delivery, naturally occurring membrane can be integrated with other synthetic materials in a manner that takes advantage of the distinct strengths of each component. Specifically, for the delivery of immunostimulants, the presence of cell membrane-derived functionality can facilitate targeting to immune cells and accumulation in immune-rich organs, while other components can be included to augment immune stimulation performance. The membrane component can be further engineered to confer exogenous functional moieties, including cytokines, receptor-binding ligands, targeting antibodies, and immunogenic antigens, among others [195]. Compared with traditional nanoformulations, a major advantage of these hybrid platforms is the ability of the natural component to camouflage artificial materials that would normally be cleared quickly by the immune system [196]. These approaches also enable sophisticated delivery strategies where different payload combinations can be employed in unique ways [197]. Additionally, in these hybrid systems, the intrinsic properties of various synthetic nanomaterials can be readily leveraged to achieve multimodal functionality or to create combinatorial treatments [115].

4.4.1 White Blood Cell Membrane Hybrids

Mimicking the function of immune cells can be an effective means for achieving targeted delivery of immunostimulatory agents for cancer therapy. The transfer of bioactive cellular components to synthetic particles is one of the strategies that can bestow the biological functions of immune cells to synthetic hybrids [198]. A bottom-up approach has been proposed based on the extraction of plasma membrane proteins from macrophages and subsequent incorporation of these proteins with synthetic choline-based phospholipids [199]. The assembled hybrid vesicles retained the targeting capability of macrophages and were used for preferential targeting to inflamed vasculature. Similarly, porous silicon particles have been cloaked using membrane derived from leukocytes [200]. The resulting hybrid particles possessed immunological functionalities similar to the source cells, including protection from opsonization, reduced phagocytic uptake, and binding to tumor endothelium. It has been shown that the source of membrane is critical for improving systemic tolerance and minimizing inflammatory responses [201]. Membrane hybrid particles derived from syngeneic membrane exhibited less uptake by the murine immune system compared with those fabricated from xenogeneic membrane, possibly due to the presence of critical biomarkers and self-recognition receptors preserved after cloaking.

A recent work described the coating of leukocyte membrane onto magnetic nanoclusters for the construction of artificial APCs [202]. Specifically, a macrophage cell line was pre-modified with azide before membrane extraction and uniformly coated onto the nanocluster cores. The nanohybrids were then functionalized with an MHC complex and anti-CD28 for antigen presentation to CD8+ T cells. The resulting artificial APCs could not only stimulate the expansion of antigen-specific CTLs, but also helped to effectively guide reinfused CTLs to tumor tissues through magnetic control. Immunotherapeutic nanoformulations cloaked by membrane from another leukocyte cell type, NK cells, have also been reported [203]. NK cells were selected because of their immunoregulatory roles. By coating polymeric nanoparticles with NK cell membrane, the resulting particles were able to induce M1 macrophage polarization and elicit tumor-specific immune responses. A photosensitizer was loaded into the polymeric cores for photodynamic therapy, which helped to improve immunotherapeutic efficacy of the system by inducing expression of damage-associated molecular patterns on dying tumor cells.

4.4.2 Red Blood Cell Membrane Hybrids

Owing to their high blood abundancy, facile processing, and remarkable biocompatibility, red blood cells (RBCs) have used extensively as a source of membrane coating material to construct versatile platforms for nanodelivery applications [204, 205]. The resulting membrane-coated nanoparticles can protect encapsulated payloads from immune clearance and facilitate enhanced delivery. As recently discovered, RBCs can help to mediate certain immune processes [206, 207], which may eventually be leveraged for immunotherapeutic applications. Their ability to interact with certain pathological immune cell subsets has also aided in the design of targeted membrane-coated nanoformulations [208]. In the work, a subpopulation of B cells was positively labelled by RBC membrane-coated nanoparticles based on cognate receptor binding. Additionally, an active particulate vaccine system based on RBC membrane-coated micromotors has recently been reported [209]. Antigen-inserted RBC membrane was integrated with core-shell micromotors that provided propulsion properties for enhanced oral vaccination. The RBC membrane-coated vaccine formulation demonstrated improved retention in the mucosal layer of the small intestine, which led to more robust antibody production.

Specifically in terms of cancer applications, an RBC membrane-based nanovaccine platform for the stimulation of antitumor immunity was recently reported [210]. The platform was constructed by enveloping RBC membrane around a polymeric PLGA core, which was used to load MPLA adjuvant and an antigenic peptide. Additionally, mannose was inserted into the RBC membrane for active APC targeting. Enhanced retention in the draining lymph nodes after intradermal injection was observed, along with elevated IFNγ secretion and CD8+ T cell responses. This nanovaccine effectively inhibited tumor growth and suppressed tumor metastasis in a murine B16F10 melanoma model.

4.4.3 Cancer Cell Membrane Hybrids

Cancer cell membrane represents a rich source of functional ligands as well as TAAs [115, 116], and these properties have been leveraged in the design of hybrid nanostructures for cancer imaging [211], photothermal therapy [212], photodynamic therapy [213], virotherapy [214], and immunotherapy [215]. In one such work on cancer immunotherapy, the immunogenic properties of HSP70 was leveraged to enhance immune responses against cancer cell membrane antigens [216]. The protein was incorporated into a membrane structure along with TAAs from B16-OVA cell membrane, which was subsequently coated around a phosphate calcium core encapsulating CpG ODN. The platform effectively delivered the antigen and adjuvant payloads to APCs and NK cells, which led to the expansion of IFNγ-expressing CD8+ T cells and NKG2D+ NK cells. In another approach, the membrane from MDA-MB-231 breast cancer cells was coated around thermally oxidized porous silica, which was used as a novel immunostimulatory agent [217]. The resulting hybrid nanoparticles greatly enhanced IFNγ secretion by peripheral blood monocytes and oriented the polarization of T cells towards a Th1 phenotype.

Without the assistance of immunostimulatory agents, the immunogenicity of TAAs is generally insufficient to elicit potent antitumor responses [218]. In addition to the above examples, there are many other strategies by which adjuvants can be included in cancer cell membrane-based nanoformulations. In an example, cell membrane from B16F10 melanoma coated onto PLGA nanoparticles was incorporated with the adjuvant MPLA [219]. Besides its ability to homotypically target the source cancer cells, this cell membrane hybrid platform could efficiently induce the maturation of professional APCs and improved downstream T cell stimulation. In a follow-up study, CpG ODN loaded into PLGA cores was used to generate another anticancer vaccine formulation (Figure 7) [220]. The nanoparticulate delivery of the adjuvant significantly enhanced its biological activity compared with CpG ODN in free form. Upon uptake by DCs, the nanovaccine formulation promoted the generation of multiple CTL populations with tumor specificity. When combined with other immunotherapies such as checkpoint blockades, the nanoformulation demonstrated the ability to significantly enhance control of tumor growth in a therapeutic setting. Over time, increasingly sophisticated nanovaccine formulations have been developed using the membrane coating concept. In a recent design, PLGA nanoparticles were loaded with the TLR7 agonist R837 and then coated with membrane from B16-OVA cancer cells (Figure 8) [221]. To provide APC targeting functionality, the membrane shell was further modified with a mannose moiety using a lipid anchoring approach. The hybrid nanoformulation not only exhibited efficacy in delaying tumor growth as a preventative vaccine, but also displayed activity against established tumors when co-administered with anti-PD-1 mAbs.

 Figure 7 

Anticancer vaccination using cancer cell membrane-coated nanoparticles (CCNPs). (A) The membrane derived from cancer cells, along with its associated tumor antigens, is coated onto CpG ODN-loaded nanoparticle cores to yield a nanoparticulate anticancer vaccine (CpG-CCNPs). Upon delivery to APCs, the vaccine formulation enables activation of T cells with multiple antitumor specificities. (B) The co-delivery of both tumor antigens and CpG together in CpG-CCNPs greatly protects against tumor growth and enhances survival. Adapted with permission from [220]. Copyright 2017 Wiley-VCH.

Theranostics Image (Click on the image to enlarge.)
 Figure 8 

Anticancer vaccination using targeted CCNPs. (A) Tumor cell membrane-coated, R837-loaded, and mannose-modified PLGA nanoparticles (NP-R@M-M) can promote transition of DCs from an immature (iDC) to mature (mDC) phenotype. (B) When combined with checkpoint blockade therapy, tumor growth can be effectively inhibited, and survival is enhanced. Adapted with permission from [221]. Copyright 2018 American Chemical Society.

Theranostics Image (Click on the image to enlarge.)

5. Conclusions and Perspectives

In this review, we have discussed current progress in the development of nanoscale platforms for the delivery of immunostimulatory agents. Adjuvants, cytokines, and mAbs all represent immunotherapeutic agents that can benefit from the enhanced transport afforded by nanodelivery. The formulation of these compounds into particulate nanocarriers protects their biological activity and elevates their bioavailability, both of which can contribute to stronger immune stimulation. To address the need for specific delivery to target immune cell subsets and immune-rich tissues, bioinspired platforms and modifications can provide certain advantages over current nanoparticle technologies. Biomimetic delivery approaches generally enable facile immune cell targeting, and the inherent immunogenicity or antigenicity associated with many of these platforms can be directly leveraged for more efficient vaccine design. Furthermore, by integrating immunostimulants with tumor antigens in the same particulate system, significant immunotherapeutic efficacy against established tumors can be achieved.

Although the emerging biomimetic approaches discussed in this review have shown significant potential for cancer immunotherapy, there are still several areas in which improvements can be made. For one, further enhancement of immunostimulatory potency in a safe manner is highly desirable. This can be achieved by improving targeting efficacy or developing new materials with better immunostimulatory characteristics. As tumor immunosuppression occurs by a variety of different mechanisms, it is likely that a large percentage of patients will not respond to mono-immunotherapies. Therefore, effort will need to be placed on the exploration of how to best combine different immunotherapeutic modalities to maximize antitumor responses. For example, agents that affect innate and adaptive immunity can be combined together to provide comprehensive immune activation. Otherwise, immunotherapies can also be combined with other therapeutic modalities, including surgery, radiation, chemotherapy, and targeted therapy, among many others. Finally, as biomimetic technologies mature, more work will need to be done in order to facilitate clinical translation. Challenges along these lines include the cost-effective sourcing of biological nanomaterials, large-scale production of pharmaceutical grade products, and optimization of long-term storage conditions. As many of these promising new platforms exist at the interface between natural and synthetic, this is a new frontier that will need to be explored in concert with regulatory agencies.

Competing Interests

The authors have declared that no competing interest exists.

References

1. Banchereau J, Briere F, Caux C, Davoust J, Lebecque S, Liu Y-J. et al. Immunobiology of dendritic cells. Annu Rev Immunol. 2000;18:767-811

2. Fang RH, Zhang L. Nanoparticle-based modulation of the immune system. Annu Rev Chem Biomol Eng. 2016;7:305-26

3. Blankenstein T, Coulie PG, Gilboa E, Jaffee EM. The determinants of tumour immunogenicity. Nat Rev Cancer. 2012;12:307-13

4. Ribas A. Adaptive immune resistance: How cancer protects from immune attack. Cancer Discov. 2015;5:915-9

5. Swann JB, Smyth MJ. Immune surveillance of tumors. J Clin Invest. 2007;117:1137-46

6. Mellman I, Coukos G, Dranoff G. Cancer immunotherapy comes of age. Nature. 2011;480:480-9

7. Pardoll DM. The blockade of immune checkpoints in cancer immunotherapy. Nat Rev Cancer. 2012;12:252-64

8. Noy R, Pollard Jeffrey W. Tumor-associated macrophages: From mechanisms to therapy. Immunity. 2014;41:49-61

9. Dranoff G. Cytokines in cancer pathogenesis and cancer therapy. Nat Rev Cancer. 2004;4:11-22

10. Dubensky TW, Reed SG. Adjuvants for cancer vaccines. Semin Immunol. 2010;22:155-61

11. Lee S, Margolin K. Cytokines in cancer immunotherapy. Cancers. 2011;3:3856-93

12. Melero I, Grimaldi AM, Perez-Gracia JL, Ascierto PA. Clinical development of immunostimulatory monoclonal antibodies and opportunities for combination. Clin Cancer Res. 2013;19:997-1008

13. Apostolico Jde S, Lunardelli VA, Coirada FC, Boscardin SB, Rosa DS. Adjuvants: Classification, modus operandi, and licensing. J Immunol Res. 2016;2016:1459394

14. Akira S, Takeda K. Toll-like receptor signalling. Nat Rev Immunol. 2004;4:499-511

15. Kawai T, Akira S. The role of pattern-recognition receptors in innate immunity: Update on Toll-like receptors. Nat Immunol. 2010;11:373-84

16. Foureau DM, Mielcarz DW, Menard LC, Schulthess J, Werts C, Vasseur V. et al. TLR9-dependent induction of intestinal α-defensins by Toxoplasma gondii. J Immunol. 2010;184:7022-9

17. Vollmer J, Weeratna R, Payette P, Jurk M, Schetter C, Laucht M. et al. Characterization of three CpG oligodeoxynucleotide classes with distinct immunostimulatory activities. Eur J Immunol. 2004;34:251-62

18. Duthie MS, Windish HP, Fox CB, Reed SG. Use of defined TLR ligands as adjuvants within human vaccines. Immunol Rev. 2011;239:178-96

19. Hopkins M, Lees BG, Richardson DG, Woroniecki SR, Wheeler AW. Standardisation of glutaraldehyde-modified tyrosine-adsorbed tree pollen vaccines containing the Th1-inducing adjuvant, monophosphoryl lipid A (MPL). Allergol Immunopathol. 2001;29:245-54

20. Mitchell MS. Perspective on allogeneic melanoma lysates in active specific immunotherapy. Semin Oncol. 1998;25:623-35

21. De Vincenzo R, Conte C, Ricci C, Scambia G, Capelli G. Long-term efficacy and safety of human papillomavirus vaccination. Int J Womens Health. 2014;6:999-1010

22. Mata-Haro V, Cekic C, Martin M, Chilton PM, Casella CR, Mitchell TC. The vaccine adjuvant monophosphoryl lipid A as a TRIF-biased agonist of TLR4. Science. 2007;316:1628-32

23. Alexopoulou L, Holt AC, Medzhitov R, Flavell RA. Recognition of double-stranded RNA and activation of NF-kB by Toll-like receptor 3. Nature. 2001;413:732-8

24. Stahl-Hennig C, Eisenblatter M, Jasny E, Rzehak T, Tenner-Racz K, Trumpfheller C. et al. Synthetic double-stranded RNAs are adjuvants for the induction of T helper 1 and humoral immune responses to human papillomavirus in rhesus macaques. PLoS Pathog. 2009;5:e1000373

25. Huleatt JW, Jacobs AR, Tang J, Desai P, Kopp EB, Huang Y. et al. Vaccination with recombinant fusion proteins incorporating Toll-like receptor ligands induces rapid cellular and humoral immunity. Vaccine. 2007;25:763-75

26. Shukla NM, Malladi SS, Mutz CA, Balakrishna R, David SA. Structure-activity relationships in human Toll-like receptor 7-active imidazoquinoline analogues. J Med Chem. 2010;53:4450-65

27. Caperton C, Berman B. Safety, efficacy, and patient acceptability of imiquimod for topical treatment of actinic keratoses. Clin Cosmet Investig Dermatol. 2011;4:35-40

28. Micali G, Lacarrubba F, Nasca MR, Ferraro S, Schwartz RA. Topical pharmacotherapy for skin cancer: Part II. Clinical applications. J Am Acad Dermatol. 2014;70(e1-12):979

29. Rosen T, Nelson A, Ault K. Imiquimod cream 2.5% and 3.75% applied once daily to treat external genital warts in men. Cutis. 2015;96:277-82

30. Barbe F, Douglas T, Saleh M. Advances in NOD-like receptors (NLR) biology. Cytokine Growth Factor Rev. 2014;25:681-97

31. Girardin SE, Boneca IG, Viala J, Chamaillard M, Labigne A, Thomas G. et al. NOD2 is a general sensor of peptidoglycan through muramyl dipeptide (MDP) detection. J Biol Chem. 2003;278:8869-72

32. Burdette DL, Monroe KM, Sotelo-Troha K, Iwig JS, Eckert B, Hyodo M. et al. STING is a direct innate immune sensor of cyclic di-GMP. Nature. 2011;478:515-8

33. Marinho FV, Benmerzoug S, Oliveira SC, Ryffel B, Quesniaux VFJ. The emerging roles of STING in bacterial infections. Trends Microbiol. 2017;25:906-18

34. Li XD, Wu J, Gao D, Wang H, Sun L, Chen ZJ. Pivotal roles of cGAS-cGAMP signaling in antiviral defense and immune adjuvant effects. Science. 2013;341:1390-4

35. Chen K, Liu J, Cao X. Regulation of type I interferon signaling in immunity and inflammation: A comprehensive review. J Autoimmun. 2017;83:1-11

36. Platanias LC. Mechanisms of type-I- and type-II-interferon-mediated signalling. Nat Rev Immunol. 2005;5:375-86

37. Lazear HM, Nice TJ, Diamond MS. Interferon-l: Immune functions at barrier surfaces and beyond. Immunity. 2015;43:15-28

38. Petrella T, Quirt I, Verma S, Haynes AE, Charette M, Bak K. et al. Single-agent interleukin-2 in the treatment of metastatic melanoma: A clinical practice guideline. Curr Oncol. 2007;14:21-6

39. Atkins MB, Regan M, McDermott D. Update on the role of interleukin 2 and other cytokines in the treatment of patients with stage IV renal carcinoma. Clin Cancer Res. 2004;10:6342S-6S

40. Thornton AM, Donovan EE, Piccirillo CA, Shevach EM. Cutting edge: IL-2 is critically required for the in vitro activation of CD4+CD25+ T cell suppressor function. J Immunol. 2004;172:6519-23

41. Del Vecchio M, Bajetta E, Canova S, Lotze MT, Wesa A, Parmiani G. et al. Interleukin-12: Biological properties and clinical application. Clin Cancer Res. 2007;13:4677-85

42. Melero I, Hervas-Stubbs S, Glennie M, Pardoll DM, Chen L. Immunostimulatory monoclonal antibodies for cancer therapy. Nat Rev Cancer. 2007;7:95-106

43. Aranda F, Vacchelli E, Eggermont A, Galon J, Fridman WH, Zitvogel L. et al. Trial watch: Immunostimulatory monoclonal antibodies in cancer therapy. OncoImmunology. 2014;3:e27297

44. Beyersdorf N, Kerkau T, Hunig T. CD28 co-stimulation in T-cell homeostasis: A recent perspective. Immunotargets Ther. 2015;4:111-22

45. Vinay DS, Kwon BS. Immunotherapy of cancer with 4-1BB. Mol Cancer Ther. 2012;11:1062-70

46. Aspeslagh S, Postel-Vinay S, Rusakiewicz S, Soria JC, Zitvogel L, Marabelle A. Rationale for anti-OX40 cancer immunotherapy. Eur J Cancer. 2016;52:50-66

47. Vonderheide RH, Glennie MJ. Agonistic CD40 antibodies and cancer therapy. Clin Cancer Res. 2013;19:1035-43

48. Cohen AD, Schaer DA, Liu C, Li Y, Hirschhorn-Cymmerman D, Kim SC. et al. Agonist anti-GITR monoclonal antibody induces melanoma tumor immunity in mice by altering regulatory T cell stability and intra-tumor accumulation. PLoS One. 2010;5:e10436

49. Sharma P, Allison JP. The future of immune checkpoint therapy. Science. 2015;348:56-61

50. Postow MA, Callahan MK, Wolchok JD. Immune checkpoint blockade in cancer therapy. J Clin Oncol. 2015;33:1974-82

51. Zhan MM, Hu XQ, Liu XX, Ruan BF, Xu J, Liao C. From monoclonal antibodies to small molecules: The development of inhibitors targeting the PD-1/PD-L1 pathway. Drug Discov Today. 2016;21:1027-36

52. Liu Y, Zheng P. How does an anti-CTLA-4 antibody promote cancer immunity?. Trends Immunol. 2018;39:953-6

53. O'Garra A, Barrat FJ, Castro AG, Vicari A, Hawrylowicz C. Strategies for use of IL-10 or its antagonists in human disease. Immunol Rev. 2008;223:114-31

54. Goldberg MV, Drake CG. LAG-3 in cancer immunotherapy. In: (ed.) Dranoff G. Cancer Immunology and Immunotherapy. Berlin, Heidelberg: Springer Berlin Heidelberg. 2011 p. 269-78

55. Anderson AC. Tim-3: An emerging target in the cancer immunotherapy landscape. Cancer Immunol Res. 2014;2:393-8

56. Manieri NA, Chiang EY, Grogan JL. TIGIT: A key inhibitor of the cancer immunity cycle. Trends Immunol. 2017;38:20-8

57. Lines JL, Sempere LF, Broughton T, Wang L, Noelle R. VISTA is a novel broad-spectrum negative checkpoint regulator for cancer immunotherapy. Cancer Immunol Res. 2014;2:510-7

58. Castellanos JR, Purvis IJ, Labak CM, Guda MR, Tsung AJ, Velpula KK. et al. B7-H3 role in the immune landscape of cancer. Am J Clin Exp Immunol. 2017;6:66-75

59. Peek LJ, Middaugh CR, Berkland C. Nanotechnology in vaccine delivery. Adv Drug Deliv Rev. 2008;60:915-28

60. Ventola CL. Cancer immunotherapy, part 2: Efficacy, safety, and other clinical considerations. P&T. 2017;42:452-63

61. Shao K, Singha S, Clemente-Casares X, Tsai S, Yang Y, Santamaria P. Nanoparticle-based immunotherapy for cancer. ACS Nano. 2015;9:16-30

62. Xiao Y, Shi K, Qu Y, Chu B, Qian Z. Engineering nanoparticles for targeted delivery of nucleic acid therapeutics in tumor. Mol Ther Methods Clin Dev. 2019;12:1-18

63. Reddy ST, van der Vlies AJ, Simeoni E, Angeli V, Randolph GJ, O'Neil CP. et al. Exploiting lymphatic transport and complement activation in nanoparticle vaccines. Nat Biotechnol. 2007;25:1159-64

64. Thomas SN, Vokali E, Lund AW, Hubbell JA, Swartz MA. Targeting the tumor-draining lymph node with adjuvanted nanoparticles reshapes the anti-tumor immune response. Biomaterials. 2014;35:814-24

65. Bertrand N, Wu J, Xu X, Kamaly N, Farokhzad OC. Cancer nanotechnology: The impact of passive and active targeting in the era of modern cancer biology. Adv Drug Deliv Rev. 2014;66:2-25

66. Dehaini D, Fang RH, Zhang L. Biomimetic strategies for targeted nanoparticle delivery. Bioeng Transl Med. 2016;1:30-46

67. Zhuang J, Fang RH, Zhang L. Preparation of particulate polymeric therapeutics for medical applications. Small Methods. 2017;1:1700147

68. Fang RH, Kroll AV, Zhang L. Nanoparticle-based manipulation of antigen-presenting cells for cancer immunotherapy. Small. 2015;11:5483-96

69. Greish K. Enhanced permeability and retention (EPR) effect for anticancer nanomedicine drug targeting. Methods Mol Biol. 2010;624:25-37

70. Chen Q, Xu L, Liang C, Wang C, Peng R, Liu Z. Photothermal therapy with immune-adjuvant nanoparticles together with checkpoint blockade for effective cancer immunotherapy. Nat Commun. 2016;7:13193

71. Sato-Kaneko F, Yao S, Ahmadi A, Zhang SS, Hosoya T, Kaneda MM. et al. Combination immunotherapy with TLR agonists and checkpoint inhibitors suppresses head and neck cancer. JCI Insight. 2017;2:e93397

72. Engel AL, Holt GE, Lu H. The pharmacokinetics of Toll-like receptor agonists and the impact on the immune system. Expert Rev Clin Pharmacol. 2011;4:275-89

73. Nuhn L, De Koker S, Van Lint S, Zhong Z, Catani JP, Combes F. et al. Nanoparticle-conjugate TLR7/8 agonist localized immunotherapy provokes safe antitumoral responses. Adv Mater. 2018;30:1803397

74. Tohme S, Simmons RL, Tsung A. Surgery for cancer: A trigger for metastases. Cancer Res. 2017;77:1548-52

75. Buchan SL, Rogel A, Al-Shamkhani A. The immunobiology of CD27 and OX40 and their potential as targets for cancer immunotherapy. Blood. 2018;131:39-48

76. Diehl L, den Boer AT, Schoenberger SP, van der Voort EI, Schumacher TN, Melief CJ. et al. CD40 activation in vivo overcomes peptide-induced peripheral cytotoxic T-lymphocyte tolerance and augments anti-tumor vaccine efficacy. Nat Med. 1999;5:774-9

77. Chen WL, Liu SJ, Leng CH, Chen HW, Chong P, Huang MH. Disintegration and cancer immunotherapy efficacy of a squalane-in-water delivery system emulsified by bioresorbable poly(ethylene glycol)-block-polylactide. Biomaterials. 2014;35:1686-95

78. Mi Y, Smith CC, Yang F, Qi Y, Roche KC, Serody JS. et al. A dual immunotherapy nanoparticle improves T-cell activation and cancer immunotherapy. Adv Mater. 2018;30:1706098

79. Broaders KE, Cohen JA, Beaudette TT, Bachelder EM, Frechet JM. Acetalated dextran is a chemically and biologically tunable material for particulate immunotherapy. Proc Natl Acad Sci USA. 2009;106:5497-502

80. Watkins-Schulz R, Tiet P, Gallovic MD, Junkins RD, Batty C, Bachelder EM. et al. A microparticle platform for STING-targeted immunotherapy enhances natural killer cell- and CD8+ T cell-mediated anti-tumor immunity. Biomaterials. 2019;205:94-105

81. Peine KJ, Bachelder EM, Vangundy Z, Papenfuss T, Brackman DJ, Gallovic MD. et al. Efficient delivery of the Toll-like receptor agonists polyinosinic:polycytidylic acid and CpG to macrophages by acetalated dextran microparticles. Mol Pharm. 2013;10:2849-57

82. Lu J, Liu X, Liao YP, Wang X, Ahmed A, Jiang W. et al. Breast cancer chemo-immunotherapy through liposomal delivery of an immunogenic cell death stimulus plus interference in the IDO-1 pathway. ACS Nano. 2018;12:11041-61

83. Meraz IM, Savage DJ, Segura-Ibarra V, Li J, Rhudy J, Gu J. et al. Adjuvant cationic liposomes presenting MPL and IL-12 induce cell death, suppress tumor growth, and alter the cellular phenotype of tumors in a murine model of breast cancer. Mol Pharm. 2014;11:3484-91

84. Zhang Y, Li N, Suh H, Irvine DJ. Nanoparticle anchoring targets immune agonists to tumors enabling anti-cancer immunity without systemic toxicity. Nat Commun. 2018;9:6

85. Seya T, Shime H, Takeda Y, Tatematsu M, Takashima K, Matsumoto M. Adjuvant for vaccine immunotherapy of cancer - Focusing on Toll-like receptor 2 and 3 agonists for safely enhancing antitumor immunity. Cancer Sci. 2015;106:1659-68

86. Song YC, Cheng HY, Leng CH, Chiang SK, Lin CW, Chong P. et al. A novel emulsion-type adjuvant containing CpG oligodeoxynucleotides enhances CD8+ T-cell-mediated anti-tumor immunity. J Control Release. 2014;173:158-65

87. Huang C-H, Huang C-Y, Cheng C-P, Dai S-H, Chen H-W, Leng C-H. et al. Degradable emulsion as vaccine adjuvant reshapes antigen-specific immunity and thereby ameliorates vaccine efficacy. Sci Rep. 2016;6:36732

88. Rahimian S, Fransen MF, Kleinovink JW, Amidi M, Ossendorp F, Hennink WE. Polymeric microparticles for sustained and local delivery of antiCD40 and antiCTLA-4 in immunotherapy of cancer. Biomaterials. 2015;61:33-40

89. Tahara Y, Akiyoshi K. Current advances in self-assembled nanogel delivery systems for immunotherapy. Adv Drug Deliv Rev. 2015;95:65-76

90. Akiyoshi K, Deguchi S, Moriguchi N, Yamaguchi S, Sunamoto J. Self-aggregates of hydrophobized polysaccharides in water. Formation and characteristics of nanoparticles. Macromolecules. 1993;26:3062-8

91. Muraoka D, Harada N, Hayashi T, Tahara Y, Momose F, Sawada S-i. et al. Nanogel-based immunologically stealth vaccine targets macrophages in the medulla of lymph node and induces potent antitumor immunity. ACS Nano. 2014;8:9209-18

92. Uenaka A, Wada H, Isobe M, Saika T, Tsuji K, Sato E. et al. T cell immunomonitoring and tumor responses in patients immunized with a complex of cholesterol-bearing hydrophobized pullulan (CHP) and NY-ESO-1 protein. Cancer Immunol Res. 2007;7:9

93. Li P, Luo Z, Liu P, Gao N, Zhang Y, Pan H. et al. Bioreducible alginate-poly(ethylenimine) nanogels as an antigen-delivery system robustly enhance vaccine-elicited humoral and cellular immune responses. J Control Release. 2013;168:271-9

94. Miyamoto N, Mochizuki S, Fujii S, Yoshida K, Sakurai K. Adjuvant activity enhanced by cross-linked CpG-oligonucleotides in β-glucan nanogel and its antitumor effect. Bioconjug Chem. 2017;28:565-73

95. Shimizu T, Kishida T, Hasegawa U, Ueda Y, Imanishi J, Yamagishi H. et al. Nanogel DDS enables sustained release of IL-12 for tumor immunotherapy. Biochem Biophys Res Commun. 2008;367:330-5

96. Hasegawa U, Sawada S-i, Shimizu T, Kishida T, Otsuji E, Mazda O. et al. Raspberry-like assembly of cross-linked nanogels for protein delivery. J Control Release. 2009;140:312-7

97. Park J, Wrzesinski SH, Stern E, Look M, Criscione J, Ragheb R. et al. Combination delivery of TGF-β inhibitor and IL-2 by nanoscale liposomal polymeric gels enhances tumour immunotherapy. Nat Mater. 2012;11:895-905

98. Dreaden EC, Austin LA, Mackey MA, El-Sayed MA. Size matters: Gold nanoparticles in targeted cancer drug delivery. Ther Deliv. 2012;3:457-78

99. Zhang P, Chiu YC, Tostanoski LH, Jewell CM. Polyelectrolyte multilayers assembled entirely from immune signals on gold nanoparticle templates promote antigen-specific T cell response. ACS Nano. 2015;9:6465-77

100. Curnis F, Fiocchi M, Sacchi A, Gori A, Gasparri A, Corti A. NGR-tagged nano-gold: A new CD13-selective carrier for cytokine delivery to tumors. Nano Res. 2016;9:1393-408

101. Meir R, Shamalov K, Sadan T, Motiei M, Yaari G, Cohen CJ. et al. Fast image-guided stratification using anti-programmed death ligand 1 gold nanoparticles for cancer immunotherapy. ACS Nano. 2017;11:11127-34

102. Emami F, Banstola A, Vatanara A, Lee S, Kim JO, Jeong JH. et al. Doxorubicin and anti-PD-L1 antibody conjugated gold nanoparticles for colorectal cancer photochemotherapy. Mol Pharm. 2019;16:1184-99

103. Wang X, Li X, Ito A, Sogo Y, Watanabe Y, Tsuji NM. et al. Biodegradable metal ion-doped mesoporous silica nanospheres stimulate anticancer Th1 immune response in vivo. ACS Appl Mater Interfaces. 2017;9:43538-44

104. An M, Li M, Xi J, Liu H. Silica nanoparticle as a lymph node targeting platform for vaccine delivery. ACS Appl Mater Interfaces. 2017;9:23466-75

105. Lu J, Liu X, Liao Y-P, Salazar F, Sun B, Jiang W. et al. Nano-enabled pancreas cancer immunotherapy using immunogenic cell death and reversing immunosuppression. Nat Commun. 2017;8:1811

106. Sidhu RS, Bollon AP. Tumor necrosis factor activities and cancer therapy — A perspective. Pharmacol Ther. 1993;57:79-128

107. Kienzle A, Kurch S, Schloder J, Berges C, Ose R, Schupp J. et al. Dendritic mesoporous silica nanoparticles for pH-stimuli-responsive drug delivery of TNF-alpha. Adv Healthcare Mater. 2017;6:1700012

108. Mercuri LP, Carvalho LV, Lima FA, Quayle C, Fantini MC, Tanaka GS. et al. Ordered mesoporous silica SBA-15: A new effective adjuvant to induce antibody response. Small. 2006;2:254-6

109. Ding B, Shao S, Yu C, Teng B, Wang M, Cheng Z. et al. Large-pore mesoporous-silica-coated upconversion nanoparticles as multifunctional immunoadjuvants with ultrahigh photosensitizer and antigen loading efficiency for improved cancer photodynamic immunotherapy. Adv Mater. 2018;30:1802479

110. Lu Y, Yang Y, Gu Z, Zhang J, Song H, Xiang G. et al. Glutathione-depletion mesoporous organosilica nanoparticles as a self-adjuvant and co-delivery platform for enhanced cancer immunotherapy. Biomaterials. 2018;175:82-92

111. Mohan T, Verma P, Rao DN. Novel adjuvants & delivery vehicles for vaccines development: A road ahead. Indian J Med Res. 2013;138:779-95

112. Bachmann MF, Jennings GT. Vaccine delivery: A matter of size, geometry, kinetics and molecular patterns. Nat Rev Immunol. 2010;10:787-96

113. Conniot J, Silva JM, Fernandes JG, Silva LC, Gaspar R, Brocchini S. et al. Cancer immunotherapy: Nanodelivery approaches for immune cell targeting and tracking. Front Chem. 2014;2:105

114. Leleux J, Roy K. Micro and nanoparticle-based delivery systems for vaccine immunotherapy: An immunological and materials perspective. Adv Healthcare Mater. 2013;2:72-94

115. Fang RH, Kroll AV, Gao W, Zhang L. Cell membrane coating nanotechnology. Adv Mater. 2018;30:1706759

116. Kroll AV, Jiang Y, Zhou J, Holay M, Fang RH, Zhang L. Biomimetic nanoparticle vaccines for cancer therapy. Adv Biosyst. 2019;3:1800219

117. Yoo JW, Irvine DJ, Discher DE, Mitragotri S. Bio-inspired, bioengineered and biomimetic drug delivery carriers. Nat Rev Drug Discov. 2011;10:521-35

118. Fang RH, Hu CM, Zhang L. Nanoparticles disguised as red blood cells to evade the immune system. Expert Opin Biol Ther. 2012;12:385-9

119. Irache JM, Salman HH, Gamazo C, Espuelas S. Mannose-targeted systems for the delivery of therapeutics. Expert Opin Drug Deliv. 2008;5:703-24

120. Taylor PR, Gordon S, Martinez-Pomares L. The mannose receptor: Linking homeostasis and immunity through sugar recognition. Trends Immunol. 2005;26:104-10

121. Jiang H-L, Kang ML, Quan J-S, Kang SG, Akaike T, Yoo HS. et al. The potential of mannosylated chitosan microspheres to target macrophage mannose receptors in an adjuvant-delivery system for intranasal immunization. Biomaterials. 2008;29:1931-9

122. Zhu S, Niu M, O'Mary H, Cui Z. Targeting of tumor-associated macrophages made possible by PEG-sheddable, mannose-modified nanoparticles. Mol Pharm. 2013;10:3525-30

123. Xu Z, Ramishetti S, Tseng Y-C, Guo S, Wang Y, Huang L. Multifunctional nanoparticles co-delivering Trp2 peptide and CpG adjuvant induce potent cytotoxic T-lymphocyte response against melanoma and its lung metastasis. J Control Release. 2013;172:259-65

124. Xu Z, Wang Y, Zhang L, Huang L. Nanoparticle-delivered transforming growth factor-β siRNA enhances vaccination against advanced melanoma by modifying tumor microenvironment. ACS Nano. 2014;8:3636-45

125. Shi G-N, Zhang C-N, Xu R, Niu J-F, Song H-J, Zhang X-Y. et al. Enhanced antitumor immunity by targeting dendritic cells with tumor cell lysate-loaded chitosan nanoparticles vaccine. Biomaterials. 2017;113:191-202

126. Wang C, Li P, Liu L, Pan H, Li H, Cai L. et al. Self-adjuvanted nanovaccine for cancer immunotherapy: Role of lysosomal rupture-induced ROS in MHC class I antigen presentation. Biomaterials. 2016;79:88-100

127. Lepenies B, Lee J, Sonkaria S. Targeting C-type lectin receptors with multivalent carbohydrate ligands. Adv Drug Deliv Rev. 2013;65:1271-81

128. Unger WWJ, van Beelen AJ, Bruijns SC, Joshi M, Fehres CM, van Bloois L. et al. Glycan-modified liposomes boost CD4+ and CD8+ T-cell responses by targeting DC-SIGN on dendritic cells. J Control Release. 2012;160:88-95

129. Roldão A, Mellado MCM, Castilho LR, Carrondo MJT, Alves PM. Virus-like particles in vaccine development. Expert Rev Vaccines. 2010;9:1149-76

130. Yan D, Wei Y-Q, Guo H-C, Sun S-Q. The application of virus-like particles as vaccines and biological vehicles. Appl Microbiol Biotechnol. 2015;99:10415-32

131. Neek M, Kim TI, Wang S-W. Protein-based nanoparticles in cancer vaccine development. Nanomedicine. 2019;15:164-74

132. Gonzalez MJ, Plummer EM, Rae CS, Manchester M. Interaction of cowpea mosaic virus (CPMV) nanoparticles with antigen presenting cells in vitro and in vivo. PLoS One. 2009;4:e7981

133. Lizotte PH, Wen AM, Sheen MR, Fields J, Rojanasopondist P, Steinmetz NF. et al. In situ vaccination with cowpea mosaic virus nanoparticles suppresses metastatic cancer. Nat Nanotechnol. 2015;11:295-303

134. Shukla S, Jandzinski M, Wang C, Gong X, Bonk KW, Keri RA. et al. A viral nanoparticle cancer vaccine delays tumor progression and prolongs survival in a HER2+ tumor mouse model. Adv Ther. 2019;2:1800139

135. Shukla S, Myers JT, Woods SE, Gong X, Czapar AE, Commandeur U. et al. Plant viral nanoparticles-based HER2 vaccine: Immune response influenced by differential transport, localization and cellular interactions of particulate carriers. Biomaterials. 2017;121:15-27

136. McCormick AA, Corbo TA, Wykoff-Clary S, Nguyen LV, Smith ML, Palmer KE. et al. TMV-peptide fusion vaccines induce cell-mediated immune responses and tumor protection in two murine models. Vaccine. 2006;24:6414-23

137. Schwarz K, Meijerink E, Speiser DE, Tissot AC, Cielens I, Renhof R. et al. Efficient homologous prime-boost strategies for T cell vaccination based on virus-like particles. Eur J Immunol. 2005;35:816-21

138. Yang L, Yang H, Rideout K, Cho T, Joo Ki, Ziegler L. et al. Engineered lentivector targeting of dendritic cells for in vivo immunization. Nat Biotechnol. 2008;26:326-34

139. Pineo CB, Hitzeroth II, Rybicki EP. Immunogenic assessment of plant-produced human papillomavirus type 16 L1/L2 chimaeras. Plant Biotechnol J. 2013;11:964-75

140. Huber B, Schellenbacher C, Jindra C, Fink D, Shafti-Keramat S, Kirnbauer R. A chimeric 18L1-45RG1 virus-like particle vaccine cross-protects against oncogenic alpha-7 human papillomavirus types. PLoS One. 2015;10:e0120152

141. Ng Q, He F, Kwang J. Recent progress towards novel EV71 anti-therapeutics and vaccines. Viruses. 2015;7:6441-57

142. Lin Y-L, Hu Y-C, Liang C-C, Lin S-Y, Liang Y-C, Yuan H-P. et al. Enterovirus-71 virus-like particles induce the activation and maturation of human monocyte-derived dendritic cells through TLR4 signaling. PLoS One. 2014;9:e111496

143. Zhang Y, Song S, Liu C, Wang Y, Xian X, He Y. et al. Generation of chimeric HBc proteins with epitopes in E. coli: Formation of virus-like particles and a potent inducer of antigen-specific cytotoxic immune response and anti-tumor effect in vivo. Cell Immunol. 2007;247:18-27

144. Ding F-X, Wang F, Lu Y-M, Li K, Wang K-H, He X-W. et al. Multiepitope peptide-loaded virus-like particles as a vaccine against hepatitis B virus-related hepatocellular carcinoma. Hepatology. 2009;49:1492-502

145. Lohcharoenkal W, Wang L, Chen YC, Rojanasakul Y. Protein nanoparticles as drug delivery carriers for cancer therapy. BioMed Res Int. 2014;2014:180549

146. Molino NM, Wang S-W. Caged protein nanoparticles for drug delivery. Curr Opin Biotechnol. 2014;28:75-82

147. Izard T, Ævarsson A, Allen MD, Westphal AH, Perham RN, de Kok A. et al. Principles of quasi-equivalence and Euclidean geometry govern the assembly of cubic and dodecahedral cores of pyruvate dehydrogenase complexes. Proc Natl Acad Sci USA. 1999;96:1240-5

148. Molino NM, Anderson AKL, Nelson EL, Wang S-W. Biomimetic protein nanoparticles facilitate enhanced dendritic cell activation and cross-presentation. ACS Nano. 2013;7:9743-52

149. Molino NM, Neek M, Tucker JA, Nelson EL, Wang S-W. Viral-mimicking protein nanoparticle vaccine for eliciting anti-tumor responses. Biomaterials. 2016;86:83-91

150. Neek M, Tucker JA, Kim TI, Molino NM, Nelson EL, Wang S-W. Co-delivery of human cancer-testis antigens with adjuvant in protein nanoparticles induces higher cell-mediated immune responses. Biomaterials. 2018;156:194-203

151. Ciocca DR, Calderwood SK. Heat shock proteins in cancer: Diagnostic, prognostic, predictive, and treatment implications. Cell Stress Chaperon. 2005;10:86-103

152. Binder RJ, Srivastava PK. HSP-APC interactions: Initiation of immune responses. In: (ed.) Asea AAA, Maio AD. Heat Shock Proteins: Potent Mediators of Inflammation and Immunity. Dordrecht: Springer Netherlands. 2007 p. 131-45

153. Crane CA, Han SJ, Ahn B, Oehlke J, Kivett V, Fedoroff A. et al. Individual patient-specific immunity against high-grade glioma after vaccination with autologous tumor derived peptides bound to the 96 kD chaperone protein. Clin Cancer Res. 2013;19:205-14

154. Mazzaferro V, Coppa J, Carrabba MG, Rivoltini L, Schiavo M, Regalia E. et al. Vaccination with autologous tumor-derived heat-shock protein gp96 after liver resection for metastatic colorectal cancer. Clin Cancer Res. 2003;9:3235-45

155. Wang X-Y, Chen X, Manjili MH, Repasky E, Henderson R, Subjeck JR. Targeted immunotherapy using reconstituted chaperone complexes of heat shock protein 110 and melanoma-associated antigen gp100. Cancer Res. 2003;63:2553-60

156. Wang Z, Gao H, Zhang Y, Liu G, Niu G, Chen X. Functional ferritin nanoparticles for biomedical applications. Front Chem Sci Eng. 2017;11:633-46

157. Han J-A, Kang YJ, Shin C, Ra J-S, Shin H-H, Hong SY. et al. Ferritin protein cage nanoparticles as versatile antigen delivery nanoplatforms for dendritic cell (DC)-based vaccine development. Nanomedicine. 2014;10:561-9

158. Benner NL, Zang X, Buehler DC, Kickhoefer VA, Rome ME, Rome LH. et al. Vault nanoparticles: Chemical modifications for imaging and enhanced delivery. ACS Nano. 2017;11:872-81

159. Kar UK, Srivastava MK, Andersson Å, Baratelli F, Huang M, Kickhoefer VA. et al. Novel CCL21-vault nanocapsule intratumoral delivery inhibits lung cancer growth. PLoS One. 2011;6:e18758

160. Feingold KR, Grunfeld C. Introduction to lipids and lipoproteins. Endotext: MDText.com, Inc. 2018

161. Kuai R, Li D, Chen YE, Moon JJ, Schwendeman A. High-density lipoproteins: Nature's multifunctional nanoparticles. ACS Nano. 2016;10:3015-41

162. Randolph GJ, Miller NE. Lymphatic transport of high-density lipoproteins and chylomicrons. J Clin Invest. 2014;124:929-35

163. Kuai R, Ochyl LJ, Bahjat KS, Schwendeman A, Moon JJ. Designer vaccine nanodiscs for personalized cancer immunotherapy. Nat Mater. 2016;16:489-96

164. Weilhammer DR, Blanchette CD, Fischer NO, Alam S, Loots GG, Corzett M. et al. The use of nanolipoprotein particles to enhance the immunostimulatory properties of innate immune agonists against lethal influenza challenge. Biomaterials. 2013;34:10305-18

165. Fischer NO, Rasley A, Corzett M, Hwang MH, Hoeprich PD, Blanchette CD. Colocalized delivery of adjuvant and antigen using nanolipoprotein particles enhances the immune response to recombinant antigens. J Am Chem Soc. 2013;135:2044-7

166. Han Y, Ding B, Zhao Z, Zhang H, Sun B, Zhao Y. et al. Immune lipoprotein nanostructures inspired relay drug delivery for amplifying antitumor efficiency. Biomaterials. 2018;185:205-18

167. Kadiyala P, Li D, Nuñez FM, Altshuler D, Doherty R, Kuai R. et al. High-density lipoprotein-mimicking nanodiscs for chemo-immunotherapy against glioblastoma multiforme. ACS Nano. 2019;13:1365-84

168. Hu Q, Li H, Wang L, Gu H, Fan C. DNA nanotechnology-enabled drug delivery systems. Chem Rev. 2019;119:6459-506

169. Li J, Pei H, Zhu B, Liang L, Wei M, He Y. et al. Self-assembled multivalent DNA nanostructures for noninvasive intracellular delivery of immunostimulatory CpG oligonucleotides. ACS Nano. 2011;5:8783-9

170. Zhang L, Zhu G, Mei L, Wu C, Qiu L, Cui C. et al. Self-assembled DNA immunonanoflowers as multivalent CpG nanoagents. ACS Appl Mater Interfaces. 2015;7:24069-74

171. Liu X, Xu Y, Yu T, Clifford C, Liu Y, Yan H. et al. A DNA nanostructure platform for directed assembly of synthetic vaccines. Nano Lett. 2012;12:4254-9

172. Wang C, Sun W, Wright G, Wang AZ, Gu Z. Inflammation-triggered cancer immunotherapy by programmed delivery of CpG and anti-PD1 antibody. Adv Mater. 2016;28:8912-20

173. Cui J, De Rose R, Best JP, Johnston APR, Alcantara S, Liang K. et al. Mechanically tunable, self-adjuvanting nanoengineered polypeptide particles. Adv Mater. 2013;25:3468-72

174. Théry C, Zitvogel L, Amigorena S. Exosomes: Composition, biogenesis and function. Nat Rev Immunol. 2002;2:569-79

175. Gao L, Wang L, Dai T, Jin K, Zhang Z, Wang S. et al. Tumor-derived exosomes antagonize innate antiviral immunity. Nat Immunol. 2018;19:233-45

176. Morishita M, Takahashi Y, Matsumoto A, Nishikawa M, Takakura Y. Exosome-based tumor antigens-adjuvant co-delivery utilizing genetically engineered tumor cell-derived exosomes with immunostimulatory CpG DNA. Biomaterials. 2016;111:55-65

177. Ochyl LJ, Bazzill JD, Park C, Xu Y, Kuai R, Moon JJ. PEGylated tumor cell membrane vesicles as a new vaccine platform for cancer immunotherapy. Biomaterials. 2018;182:157-66

178. Cheung AS, Koshy ST, Stafford AG, Bastings MMC, Mooney DJ. Adjuvant-loaded subcellular vesicles derived from disrupted cancer cells for cancer vaccination. Small. 2016;12:2321-33

179. Wu T, Qi Y, Zhang D, Song Q, Yang C, Hu X. et al. Bone marrow dendritic cells derived microvesicles for combinational immunochemotherapy against tumor. Adv Funct Mater. 2017;27:1703191

180. Ochyl LJ, Moon JJ. Dendritic cell membrane vesicles for activation and maintenance of antigen-specific T cells. Adv Healthcare Mater. 2019;8:1801091

181. Wang S, Gao J, Wang Z. Outer membrane vesicles for vaccination and targeted drug delivery. Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2019;11:e1523

182. van der Pol L, Stork M, van der Ley P. Outer membrane vesicles as platform vaccine technology. Biotechnol J. 2015;10:1689-706

183. Tan K, Li R, Huang X, Liu Q. Outer membrane vesicles: Current status and future direction of these novel vaccine adjuvants. Front Microbiol. 2018;9:783

184. Kim OY, Park HT, Dinh NTH, Choi SJ, Lee J, Kim JH. et al. Bacterial outer membrane vesicles suppress tumor by interferon-γ-mediated antitumor response. Nat Commun. 2017;8:626

185. Nastala CL, Edington HD, McKinney TG, Tahara H, Nalesnik MA, Brunda MJ. et al. Recombinant IL-12 administration induces tumor regression in association with IFN-gamma production. J Immunol. 1994;153:1697-706

186. Lasek W, Zagożdżon R, Jakobisiak M. Interleukin 12: Still a promising candidate for tumor immunotherapy?. Cancer Immunol Immunother. 2014;63:419-35

187. Nagarajan S, Selvaraj P. Human tumor membrane vesicles modified to express glycolipid-anchored IL-12 by protein transfer induce T cell proliferation in vitro : A potential approach for local delivery of cytokines during vaccination. Vaccine. 2006;24:2264-74

188. Patel JM, Vartabedian VF, Bozeman EN, Caoyonan BE, Srivatsan S, Pack CD. et al. Plasma membrane vesicles decorated with glycolipid-anchored antigens and adjuvants via protein transfer as an antigen delivery platform for inhibition of tumor growth. Biomaterials. 2016;74:231-44

189. Zhang X, Wang C, Wang J, Hu Q, Langworthy B, Ye Y. et al. PD-1 blockade cellular vesicles for cancer immunotherapy. Adv Mater. 2018;30:1707112

190. Zhang X, Wang J, Chen Z, Hu Q, Wang C, Yan J. et al. Engineering PD-1-presenting platelets for cancer immunotherapy. Nano Lett. 2018;18:5716-25

191. Zhang P, Chen Y, Zeng Y, Shen C, Li R, Guo Z. et al. Virus-mimetic nanovesicles as a versatile antigen-delivery system. Proc Natl Acad Sci USA. 2015;112:E6129-E38

192. Liu X, Yuan L, Zhang L, Mu Y, Li X, Liu C. et al. Bioinspired artificial nanodecoys for hepatitis B virus. Angew Chem Int Ed. 2018;57:12499-503

193. Zhang P, Zhang L, Qin Z, Hua S, Guo Z, Chu C. et al. Genetically engineered liposome-like nanovesicles as active targeted transport platform. Adv Mater. 2018;30:1705350

194. Grandi A, Tomasi M, Zanella I, Ganfini L, Caproni E, Fantappiè L. et al. Synergistic protective activity of tumor-specific epitopes engineered in bacterial outer membrane vesicles. Front Oncol. 2017;7:253

195. Saeui CT, Mathew MP, Liu L, Urias E, Yarema KJ. Cell surface and membrane engineering: Emerging technologies and applications. J Funct Biomater. 2015;6:454-85

196. Hu C-MJ, Zhang L, Aryal S, Cheung C, Fang RH, Zhang L. Erythrocyte membrane-camouflaged polymeric nanoparticles as a biomimetic delivery platform. Proc Natl Acad Sci USA. 2011;108:10980-5

197. Cheng H, Jiang X-Y, Zheng R-R, Zuo S-J, Zhao L-P, Fan G-L. et al. A biomimetic cascade nanoreactor for tumor targeted starvation therapy-amplified chemotherapy. Biomaterials. 2019;195:75-85

198. Buddingh' BC, van Hest JCM. Artificial cells: Synthetic compartments with life-like functionality and adaptivity. Acc Chem Res. 2017;50:769-77

199. Molinaro R, Corbo C, Martinez JO, Taraballi F, Evangelopoulos M, Minardi S. et al. Biomimetic proteolipid vesicles for targeting inflamed tissues. Nat Mater. 2016;15:1037-46

200. Parodi A, Quattrocchi N, van de Ven AL, Chiappini C, Evangelopoulos M, Martinez JO. et al. Synthetic nanoparticles functionalized with biomimetic leukocyte membranes possess cell-like functions. Nat Nanotechnol. 2012;8:61-8

201. Evangelopoulos M, Parodi A, Martinez JO, Yazdi IK, Cevenini A, van de Ven AL. et al. Cell source determines the immunological impact of biomimetic nanoparticles. Biomaterials. 2016;82:168-77

202. Zhang Q, Wei W, Wang P, Zuo L, Li F, Xu J. et al. Biomimetic magnetosomes as versatile artificial antigen-presenting cells to potentiate T-cell-based anticancer therapy. ACS Nano. 2017;11:10724-32

203. Deng G, Sun Z, Li S, Peng X, Li W, Zhou L. et al. Cell-membrane immunotherapy based on natural killer cell membrane coated nanoparticles for the effective inhibition of primary and abscopal tumor growth. ACS Nano. 2018;12:12096-108

204. Gao W, Zhang L. Engineering red-blood-cell-membrane-coated nanoparticles for broad biomedical applications. AIChE J. 2015;61:738-46

205. Zhuang J, Ying M, Spiekermann K, Holay M, Zhang Y, Chen F. et al. Biomimetic nanoemulsions for oxygen delivery in vivo. Adv Mater. 2018;30:1804693

206. Karsten E, Breen E, Herbert BR. Red blood cells are dynamic reservoirs of cytokines. Sci Rep. 2018;8:3101

207. Nombela I, Ortega-Villaizan MdM. Nucleated red blood cells: Immune cell mediators of the antiviral response. PLoS Pathog. 2018;14:e1006910

208. Luk BT, Jiang Y, Copp JA, Hu C-MJ, Krishnan N, Gao W. et al. Biomimetic targeting of nanoparticles to immune cell subsets via cognate antigen interactions. Mol Pharm. 2018;15:3723-8

209. Wei X, Beltrán-Gastélum M, Karshalev E, Esteban-Fernández de Ávila B, Zhou J, Ran D. et al. Biomimetic micromotor enables active delivery of antigens for oral vaccination. Nano Lett. 2019;19:1914-21

210. Guo Y, Wang D, Song Q, Wu T, Zhuang X, Bao Y. et al. Erythrocyte membrane-enveloped polymeric nanoparticles as nanovaccine for induction of antitumor immunity against melanoma. ACS Nano. 2015;9:6918-33

211. Rao L, Bu L-L, Cai B, Xu J-H, Li A, Zhang W-F. et al. Cancer cell membrane-coated upconversion nanoprobes for highly specific tumor imaging. Adv Mater. 2016;28:3460-6

212. Chen Z, Zhao P, Luo Z, Zheng M, Tian H, Gong P. et al. Cancer cell membrane-biomimetic nanoparticles for homologous-targeting dual-modal imaging and photothermal therapy. ACS Nano. 2016;10:10049-57

213. Yu Z, Zhou P, Pan W, Li N, Tang B. A biomimetic nanoreactor for synergistic chemiexcited photodynamic therapy and starvation therapy against tumor metastasis. Nat Commun. 2018;9:5044

214. Lv P, Liu X, Chen X, Liu C, Zhang Y, Chu C. et al. Genetically engineered cell membrane nanovesicles for oncolytic adenovirus delivery: A versatile platform for cancer virotherapy. Nano Lett. 2019;19:2993-3001

215. Liu W-L, Zou M-Z, Liu T, Zeng J-Y, Li X, Yu W-Y. et al. Expandable immunotherapeutic nanoplatforms engineered from cytomembranes of hybrid cells derived from cancer and dendritic cells. Adv Mater. 2019;31:1900499

216. Kang T, Huang Y, Zhu Q, Cheng H, Pei Y, Feng J. et al. Necroptotic cancer cells-mimicry nanovaccine boosts anti-tumor immunity with tailored immune-stimulatory modality. Biomaterials. 2018;164:80-97

217. Fontana F, Shahbazi M-A, Liu D, Zhang H, Mäkilä E, Salonen J. et al. Multistaged nanovaccines based on porous silicon@acetalated dextran@cancer cell membrane for cancer immunotherapy. Adv Mater. 2017;29:1603239

218. Zalba S, ten Hagen TLM. Cell membrane modulation as adjuvant in cancer therapy. Cancer Treat Rev. 2017;52:48-57

219. Fang RH, Hu C-MJ, Luk BT, Gao W, Copp JA, Tai Y. et al. Cancer cell membrane-coated nanoparticles for anticancer vaccination and drug delivery. Nano Lett. 2014;14:2181-8

220. Kroll AV, Fang RH, Jiang Y, Zhou J, Wei X, Yu CL. et al. Nanoparticulate delivery of cancer cell membrane elicits multiantigenic antitumor immunity. Adv Mater. 2017;29:1703969

221. Yang R, Xu J, Xu L, Sun X, Chen Q, Zhao Y. et al. Cancer cell membrane-coated adjuvant nanoparticles with mannose modification for effective anticancer vaccination. ACS Nano. 2018;12:5121-9

Author contact

Corresponding address Corresponding authors: J. Zhang: jie.zhangcom and L. Zhang. zhangedu


Received 2019-6-2
Accepted 2019-6-26
Published 2019-10-15