Theranostics 2021; 11(4):1690-1702. doi:10.7150/thno.53691


The 2020 race towards SARS-CoV-2 specific vaccines

Tomasz M. Karpiński1 Corresponding address, Marcin Ożarowski2, Agnieszka Seremak-Mrozikiewicz3,4,5, Hubert Wolski3,6, Donald Wlodkowic7

1. Chair and Department of Medical Microbiology, Poznań University of Medical Sciences, Wieniawskiego 3, 61-712 Poznań, Poland.
2. Department of Biotechnology, Institute of Natural Fibres and Medicinal Plants, Poznań, Poland.
3. Division of Perinatology and Women's Disease, Poznań University of Medical Sciences, Poznań, Poland.
4. Laboratory of Molecular Biology in Division of Perinatology and Women's Diseases, Poznań University of Medical Sciences, Poznań, Poland.
5. Department of Pharmacology and Phytochemistry, Institute of Natural Fibres and Medicinal Plants, Poznań, Poland.
6. Division of Obstetrics and Gynecology, Tytus Chałubiński's Hospital, Zakopane, Poland.
7. School of Science, RMIT University, Melbourne, VIC, Australia.

This is an open access article distributed under the terms of the Creative Commons Attribution License ( See for full terms and conditions.
Karpiński TM, Ożarowski M, Seremak-Mrozikiewicz A, Wolski H, Wlodkowic D. The 2020 race towards SARS-CoV-2 specific vaccines. Theranostics 2021; 11(4):1690-1702. doi:10.7150/thno.53691. Available from

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The global outbreak of a novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) highlighted a requirement for two pronged clinical interventions such as development of effective vaccines and acute therapeutic options for medium-to-severe stages of “coronavirus disease 2019" (COVID-19). Effective vaccines, if successfully developed, have been emphasized to become the most effective strategy in the global fight against the COVID-19 pandemic. Basic research advances in biotechnology and genetic engineering have already provided excellent progress and groundbreaking new discoveries in the field of the coronavirus biology and its epidemiology. In particular, for the vaccine development the advances in characterization of a capsid structure and identification of its antigens that can become targets for new vaccines. The development of the experimental vaccines requires a plethora of molecular techniques as well as strict compliance with safety procedures. The research and clinical data integrity, cross-validation of the results, and appropriated studies from the perspective of efficacy and potently side effects have recently become a hotly discussed topic.

In this review, we present an update on latest advances and progress in an ongoing race to develop 52 different vaccines against SARS-CoV-2. Our analysis is focused on registered clinical trials (current as of November 04, 2020) that fulfill the international safety and efficacy criteria in the vaccine development. The requirements as well as benefits and risks of diverse types of SARS-CoV-2 vaccines are discussed including those containing whole-virus and live-attenuated vaccines, subunit vaccines, mRNA vaccines, DNA vaccines, live vector vaccines, and also plant-based vaccine formulation containing coronavirus-like particle (VLP). The challenges associated with the vaccine development as well as its distribution, safety and long-term effectiveness have also been highlighted and discussed.

Keywords: severe acute respiratory syndrome coronavirus 2, SARS-CoV-2, coronavirus disease 2019, COVID-19, vaccine, clinical trials


In December 2019, the first cases of human infections by the zoonotic SARS-CoV-2 (initially named 2019-nCoV) were reported. Those initially occurred in Wuhan (China) and centered on a population of wet market traders where live seafood, as well as live farmed and wild animals, were commonly sold [1]. The virus causes a respiratory disease named as coronavirus disease 2019 (COVID-19) [2]. The number of infected patients has continued to increase at an alarming rate. In comparison from December 31, 2019, up to August 25, 2020, 23,673,902 cases of COVID-19 have been reported worldwide. More than two months later, up to November 04, 2020, there were double the number of infected patients, with 47,594,234 cases of COVID-19 and 1 215 892 deaths. On November 04, 2020, the highest numbers of patients with COVID-19 was stated in the United States (9,383,979), India (8,313,876), Brazil (5,566,049) and Russia (1,673,686) [3].

Similar to historical experience with majority of respiratory track infectious diseases, compliance with hygiene guidelines can only slow down the overall number of infections due to restriction of exposure pathways. An effective vaccine, if successfully developed, has been broadly emphasized to become the most effective strategy in the global fight against COVID-19 pandemic.

In this review, we present a critical update on latest advances and progress in an ongoing race to develop 51 different vaccines against SARS-CoV-2. The motivation of our work is to provide an up-to-date analysis focused on registered clinical trials (current as of November 04, 2020) that fulfill the international safety and efficacy criteria in the vaccine development. The data were obtained from six clinical trial registries of the European Union [4], India [5], China [6], Australia and New Zealand [7], Clinical Trials of US National Library of Medicine [8], Pan African Clinical Trials Registry [9], Cuban Registry of Clinical Trials [10], Indonesia Registry [11], and ISRCTN [12].

We discuss the requirements as well as benefits and risks of diverse types of SARS-CoV-2 vaccines are discussed including those containing whole-virus and live-attenuated vaccines, subunit vaccines, mRNA vaccines, DNA vaccines, live vector vaccines, and also plant-based vaccine formulation containing coronavirus-like particle (VLP). The challenges associated with the vaccine development as well as its distribution, safety and long-term effectiveness have also been highlighted and discussed.

SARS-CoV-2 biology

Coronaviruses name comes from a characteristic image that resembles a solar corona when observed using a transmission electron microscope [13]. Today over seven human coronaviruses have been identified. Four of them characterized by relatively low pathogenicity are HCoV-229E, HCoV-OC43, HCoV-NL63, and HCoV-HKU1. They are responsible for seasonal and usually mild infections of the upper respiratory tract. These four coronaviruses are responsible for up to 15-30% of common colds in adults [14]. The remaining are the highly pathogenic SARS-CoV-1, MERS-CoV, and SARS-CoV-2 viruses, responsible for severe lower respiratory tract infections. Human coronaviruses are now classified into the kingdom Riboviria, order Nidovirales, family Coronaviridae and the subfamily Orthocoronavirinae [15]. Four genera are distinguished in this subfamily: Alphacoronavirus, Betacoronavirus, Deltacoronavirus, and Gammacoronavirus. Viruses 229E and NL63 belong to Alphacoronaviruses, while OC43, HKU1, SARS-CoV-1, MERS-CoV, and SARS-CoV-2 belong to Betacoronaviruses. Alpha- and Beta-coronaviruses can cause infections in various species of mammals, including humans, but population of bats is their natural habitat. Wild birds are a common reservoir of delta- and gamma-coronaviruses. One of the most dangerous features of coronaviruses is their capability to break through the species barrier. In this regard, a plethora of reports demonstrated transfers from wild to domestic birds and some species of mammals, including even marine mammals [16,17].

SARS-CoV-2 has single-stranded, non-segmented RNA of positive polarity (+ ssRNA). RNA can act directly as mRNA in protein translation [15]. SARS-CoV-2 belongs to a new evolutionary branch within the genus Betacoronavirus and has 79% genetic similarity with SARS-CoV and nearly 50% similarity with MERS-CoV [18]. Phylogenetic analyses showed that SARS-CoV-2 is closely related (88% similarity) to two coronaviruses occurring in bats, namely bat-SL-CoVZC45 and bat-SL-CoVZXC21. Bats are likely the natural hosts for SARS-CoV-2, and pangolins can be one of the intermediate hosts significant to viral transfer to humans [19,20]. SARS-CoV-2 can be transmitted directly from person to person. Main ways are close contact and emission of respiratory droplets by infected person during coughs or sneezes. The virus can also be transmitted indirectly by touching contaminated surfaces or objects and touching the face, eyes, or mouth [21].

Antigens of SARS-COV-2

The antigens of the virus include all of its elements, including proteins, lipids, polysaccharide, and nucleic acids. The whole-cell antigens are used for developing the whole virus killed and live-attenuated vaccines [22].

Major structural proteins: spike protein (S), nucleocapsid protein (N), membrane glycoprotein (M), and envelope protein (E) can be distinguished in the SARS-CoV-2 structure (Figure 1).

Spike glycoprotein (S)

The S protein is surface fusion glycoprotein, which can be directly recognized by the host immune system. It gives the virion a corona or crown-like appearance [23]. Protein S mediates the entry of the virus into host cells. The mechanisms of SARS-CoV-2 infection rely on the entry of the virus into human cells by angiotensin-converting enzyme 2 (ACE2) receptor [2,24]. The virus attacks mainly epithelial cells in the respiratory and gastrointestinal tracts [25]. Binding capacity to the ACE2 receptor is approximately 10-20 times stronger in the case of SARS-CoV-2 than the SARS-CoV. Simultaneously, the density of the ACE2 is higher in adults than in children [26]. This can potentially explain why adults have a higher predisposition to infection and severe disease in comparison to children.

 Figure 1 

The structure of SARS-CoV-2. This coronavirus is an enveloped, positive-sense RNA virus and contains four main structural proteins, including spike (S), membrane (M), envelope (E) and nucleocapsid (N) proteins.

Theranostics Image (Click on the image to enlarge.)

The S protein forms a trimer on the viral membrane and consists of two subunits (S1 and S2) [23]. The S1 subunit contains two domains such as the N-terminal domain (NTD) and the C-terminal domain (CTD). The latter includes the receptor-binding domain (RBD). RBD is responsible for host cell receptor binding. The S2 subunit facilitates membrane fusion between the viral and host cell membranes [27]. The S protein binds to the angiotensin-converting enzyme 2 (ACE2) receptor and directly facilitates viral entry [25]. It is studied for use as antigens in vaccines both as full-length S protein, and also as the RBD domain, the S1 subunit, and NTD [22]. The S protein is one of the essential immunodominant proteins of coronaviruses, inducing host immune responses [28]. This glycoprotein is the most often target for SARS-CoV-2 developed vaccines, including adenoviral, RNA-based, DNA-based, and protein subunit vaccines [29].

Nucleocapsid protein (N)

The N protein has multiple functions. Self-association of the N protein is required for the packaging the viral genome and formation of the viral capsid. It is also involved in virus budding, RNA replication, and mRNA transcription [30]. The N protein can inhibit the activity of cyclin-cyclin-dependent kinase (cyclin-CDK) complex, which leads to inhibition of S phase (genome replication) progression in the mammalian cell cycle [31]. The N protein of SARS-CoV can activate an AP-1 pathway, which regulates many cellular processes, including cell proliferation, differentiation, and apoptosis [32]. Nucleocapsid protein can also inhibit type I interferon (IFN) and immune responses and simultaneously activate cyclooxygenase-2 (COX-2) leading to inflammation in the lungs [33].

Membrane glycoprotein (M)

The M protein is a transmembrane glycoprotein and has three transmembrane domains. It binds to the nucleocapsid and is involved in virus assembly [34]. It interacts with the N protein to encapsulate the RNA genome and generate virions [35]. The M protein can inhibit production of COX-2 and activation of nuclear factor kappa B (NFκB), thus enhancing the viral proliferation [33]. In the SARS virus, this protein has been reported to induce apoptosis by through the canonical caspases cascade [36].

Envelope protein (E)

The E protein is a small membrane protein with reported ion channel activity [37]. This protein also plays a role in viral assembly, virion release, and viral pathogenesis [34]. This protein was reported to have viroporin activity, and can mediate pathogenic processes and induce cytotoxicity [33]. In contrast to other major structural proteins, the E protein is not suitable for use as an immunogen [22]. The E protein affects the production of pro-inflammatory cytokines IL-1, IL-6 and TNF [38].

Types of SARS-CoV-2 vaccines

The vaccine against SARS-CoV-2 should meet at least the following requirements: minimize undesired immunopotentiation, be suitable for adult healthcare workers, be suitable for adults > 60 years old or with underlying diabetes or hypertension, and be suitable for long-term stockpiling [39].

As of November 04, 2020, fifty-two vaccines against SARS-CoV-2 are undergoing clinical trials, including 9 in Phase 3, three in Phase 2, 18 in Phase 1/2 and 22 in Phase 1 (Table 1). These include 13 protein subunit candidates, 11 non-replicating viral vector vaccines, 6 inactivated, 6 RNA and 4 DNA vaccines, four replicating viral vectored, two virus-like protein (VLP), and 6 others (Figures 2A,B & Figure 3). In Phase 1 are vaccines in small-scale safety, given to a small group of volunteers, in Phase 2 are vaccines in expanded safety, given to hundreds of volunteers, in Phase 3 are vaccines in large-scale safety and efficacy, given to thousands of volunteers [40].

 Figure 2 

Number of vaccine candidates against SARS-CoV-2 in (A) clinical and (B) preclinical development, selected according to vaccine platform technology. Classical (conventional) platforms include the inactivated virus, live attenuated virus, protein subunit, and virus-like particle vaccines. To the next-generation platforms belong viral vectored, RNA, DNA and antigen-presenting cells vaccines.

Theranostics Image (Click on the image to enlarge.)
 Table 1 

Clinical trials of SARS-CoV-2 vaccines, current as of October 19, 2020

Name of vaccineType of vaccineStage of clinical trialIdentifierDeveloper/manufacturer
SinovacInactivatedPhase 3NCT04582344Sinovac Research and Development Co., Ltd./Butantan Institute/Health Institutes of Turkey.
Phase 3NCT04456595
Phase 1/2NCT04551547
Phase 1/2NCT04352608
Phase 1/2NCT04383574
COVID-19 vaccine (Vero cells)InactivatedPhase 3ChiCTR2000039000Wuhan Institute of Biological Products Co., Ltd./Sinopharm,
Phase 3ChiCTR2000034780
Phase 1/2ChiCTR2000031809
Phase 3NCT04560881Beijing Institute of Biological Products Co., Ltd.
Phase 1/2ChiCTR2000032459
NVX-CoV2373/SARS-CoV-2 rS/Matrix-M1 AdjuvantRecombinant S protein subunit with matrix-M adjuvantPhase 3EudraCT 2020-004123-16Novavax
Phase 3NCT04611802
Phase 2NCT04533399
Phase 1NCT04368988
mRNA-1273Lipid nanoparticle (LNP)-encapsulated mRNAPhase 3NCT04470427Moderna TX, Inc./National Institute of Allergy and Infectious Diseases.
Phase 2NCT04405076
Phase 1NCT04283461
ChAdOx1 nCoV-19/AZD1222Non-replicating adenovirus vectoredPhase 3NCT04540393University of Oxford/Astra Zeneca/Serum Institute of India
Phase 3NCT04516746
Phase 3ISRCTN89951424
Phase 2/3CTRI/2020/08/027170
Phase 2/3NCT04400838
Phase 2/3EudraCT 2020-001228-32
Phase 1/2NCT04324606
Phase 1/2EudraCT 2020-001072-15
Phase 1/2PACTR202006922165132
Phase 1/2NCT04444674University of Witwatersrand, South Africa
Ad26.COV2.SNon-replicating adenovirus 26 vectoredPhase 3NCT04505722Janssen Vaccines & Prevention B.V.
Phase 1/2NCT04436276
Ad5-nCoVNon-replicating adenovirus type 5 vectoredPhase 3NCT04540419Insitute of Biotechnology, Academy of Military Medical Sciences, PLA of China/CanSino Biologics Inc.
Phase 3NCT04526990
Phase 2NCT04566770
Phase 2ChiCTR2000031781
Phase 2NCT04341389
Phase 1/2NCT04398147
Phase 1ChiCTR2000030906
Phase 1NCT04552366
Phase 1NCT04313127
Gam-COVID-VacNon-replicating adenovirus 5 and 26 vectoredPhase 3NCT04564716Gamaleya Research Institute of Epidemiology and Microbiology, Health Ministry of the Russian Federation.
Phase 3NCT04530396
Phase 2NCT04587219
Phase 1/2NCT04436471
Phase 1/2NCT04437875
BNT162a, BNT162bNucleoside-modified mRNAPhase 2/3NCT04368728BioNTech/Fosun Pharma/Pfizer
Phase 1/2NCT04537949
Phase 1/2EudraCT 2020-001038-36
Phase 1/2NCT04380701
Phase 1ChiCTR2000034825
SARS-CoV-2 Vaccine (Vero Cells)InactivatedPhase 2ChiCTR2000039462Shenzhen Kangtai Biological Products Co., Ltd./Beijing Minhai Biotechnology Co., Ltd.
Phase 1ChiCTR2000038804
2019-nCOV vaccineNon-replicating adenovirus vectoredPhase 2ChiCTR2000031781Insitute of Biotechnology, Academy of Military Medical Sciences, PLA of China
Phase 1ChiCTR2000030906
Vaccine (CHO cell)Recombinant RBD protein subunitPhase 2NCT04466085Anhui Zhifei Longcom Biologic Pharmacy Co., Ltd.
Phase 1/2NCT04550351
Phase 1NCT04445194
CVnCoVmRNAPhase 2NCT04515147CureVac AG
Phase 1NCT04449276
INO-4800DNA plasmidPhase 1/2NCT04447781Inovio Pharmaceuticals/International Vaccine Institute
Phase 1NCT04336410
nCov vaccineDNA plasmidPhase 1/2CTRI/2020/07/026352Cadila Healthcare Ltd.
GX-19DNAPhase 1/2NCT04445389Genexine, Inc.
AG0301-COVID19DNA plasmidPhase 1/2NCT04527081AnGes, Inc.
Phase 1/2NCT04463472
BBV152Whole virion inactivatedPhase 1/2CTRI/2020/09/027674Bharat Biotech International Ltd.
Phase 1/2CTRI/2020/07/026300
Phase 1/2NCT04471519
no nameInactivatedPhase 1/2NCT04470609Chinese Academy of Medical Sciences
Phase 1/2NCT04412538
QazCovid-inInactivatedPhase 1/2NCT04530357Research Institute for Biological Safety Problems
V-SARSPill vaccine from heat-inactivated plasma of donors with COVID-19Phase 1/2NCT04380532Immunitor LLC
AV-COVID-19Autologous dendritic cells loaded with antigens from SARS-CoV-2Phase 1/2NCT04386252Aivita Biomedical, Inc.
EpiVacCoronaProtein subunitPhase 1/2NCT04527575Federal Budgetary Research Institution State Research Center of Virology and Biotechnology “Vector”.
no nameProtein subunitPhase 1/2NCT04537208Sanofi Pasteur/GlaxoSmithKline
KBP-COVID-19RBD protein subunitPhase 1/2NCT04473690Kentucky BioProcessing, Inc.
FINLAY-FR-1RBD protein subunitPhase 1/2IFV/COR/04Finlay Vaccine Institute
RBD SARS-CoV-2 HBsAg VLPVLPPhase 1/2ACTRN12620000817943Serum Institute of India
ARCT-021Lipid nanoparticle (LNP)-mRNAPhase 1/2NCT04480957Arcturus Therapeutics, Inc.
AlloStimBioengineered allogeneic cellular vaccine derived from healthy blood donorsPhase 1/2NCT04441047Immunovative Therapies, Ltd.
LV-SMENP-DCMinigenes engineered based on multiple viral genes, lentiviral vectored (NHP/TYF)Phase 1/2NCT04276896Shenzhen Geno-Immune Medical Institute
rVSV-SARS-CoV-2-S/IIBR-100Replicating viral
VSV vectored
Phase 1/2NCT04608305Israel Institute for Biological Research
Pathogen-specific aAPCMinigenes engineered based on multiple viral genes, lentiviral vectored (NHP/TYF)Phase 1NCT04299724Shenzhen Geno-Immune Medical Institute
defective Simian adenovirus vectored
Phase 1NCT04528641ReiThera Srl
adenovirus Ad5 vectored
Phase 1NCT04591717ImmunityBio, Inc.
adenovirus Ad5 vectored
Phase 1NCT04563702Vaxart
modified vaccinia virus Ankara vectored
Phase 1NCT04569383Universitätsklinikum Hamburg-Eppendorf
intranasal based-RBD flu vectored
Phase 1ChiCTR2000037782Beijing Wantai Biological Pharmacy
TMV-083Replicating measles-vector basedPhase 1NCT04497298Institut Pasteur/Themis Bioscience/Coalition for Epidemic Preparedness Innovations
V590Replicating VSV-vector basedPhase 1NCT04569786Merck Sharp & Dohme Corp.
no namemRNAPhase 1ChiCTR2000039212Yunnan Walvax Biotechnology Co., Ltd.
Phase 1ChiCTR2000034112
LNP-nCoVsaRNALipid nanoparticle (LNP)-RNAPhase 1ISRCTN17072692Imperial College London
no nameRecombinant chimeric DC vaccinePhase 1ChiCTR2000030750Shenzhen Third People's Hospital
pVACProtein subunitPhase 1NCT04546841University Hospital Tuebingen
UB-612RBD protein subunitPhase 1NCT04545749United Biomedical Inc./COVAXX
Recombinant vaccine (Sf9)RBD protein subunitPhase 1ChiCTR2000037518West China Hospital, Sichuan University
SCB-2019Trimeric spike protein subunitPhase 1NCT04405908Clover Biopharmaceuticals AUS Pty Ltd
Covax-19Recombinant spike protein subunit with Advax-SM adjuvantPhase 1NCT04428073GeneCure Biotechnologies
Phase 1NCT04453852Vaxine Pty Ltd
no nameSpike protein subunit with MF59 adjuvantPhase 1ISRCTN51232965University of Queensland
MVC-COV1901S protein subunitPhase 1NCT04487210Medigen Vaccine Biologics Corp.
no namePlant-derived coronavirus-like particle (VLP)Phase 1NCT04450004Medicago
bacTRL-SpikeLive Bifidobacterium longum, engineered to deliver DNA plasmidsPhase 1NCT04334980Symvivo Corporation
no nameNucleocapsid-GM-CSF protein lactated Ringer's injectionEarly Phase 1NCT03305341,
Han Xu, Sponsor-Investigator, IRB Chair, Medicine Invention Design, Inc.

Data obtained from clinical trial registries of the European Union [4], India [5], China [6], Australia and New Zealand [7], Clinical Trials of US National Library of Medicine [8], Pan African Clinical Trials Registry [9], Cuban Registry of Clinical Trials [10], Indonesia Registry [11], and ISRCTN [12].

 Figure 3 

Number of candidates of SARS-CoV-2 vaccines by phase of clinical trial. As of November 04, 2020, fifty-two vaccines against SARS-CoV-2 are undergoing clinical trials, including 22 in Phase 1, 18 in Phase 1/2, three in Phase 2, and 9 in Phase 3.

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 Table 2 

Some characteristics of selected candidate vaccines against SARS-CoV-2 [86,89-91]

Type of vaccineAdvantagesDisadvantagesUsed examples against other pathogens
InactivatedEasy to prepare; proven technology; safety; multivalent; no adjuvants required; induce strong immune responsesPotential inappropriate for persons with immunosuppression; complicated to scale up manufacturingPolio
Live-AttenuatedRapid development; proven technology; multivalent; no adjuvants required; induce strong immune responsesPossibility of reversion; risk for infection; complicated to scale up manufacturingMeasles, Mumps, Rubella, Chickenpox
SubunitSafety; consistent production; induce strong cellular and humoral immune responsesHigh cost; lower immunogenicity; require repeated doses and adjuvants; complicated to scale up manufacturingPertussis, Hepatitis B, Influenza
Viral Vector-BasedSafety; induces strong cellular and humoral responsesPotential risk for infection, chromosomal integration and oncogenesis; possibly present pre-existing immunity against the vector; risk for inflammatory adverse reactionsEbola
RNASafety; rapid development and production; no risk of genetic integration; possibility of multivalency; induce strong immune responses, both humoral and cell-mediatedUnstable under physiological conditions; possibility of inflammatory reactions; risk for adverse reactions; high costNot currently licensed
DNASafety; rapid development and production; possibility of multivalency; immune response, both humoral and cell-mediated; long-term stability; possibility of oral formulationPoor immune responses in humans; repeated doses may cause toxicity; potential risk of genetic integationNot currently licensed
 Figure 4 

Classical and next-generation vaccine platforms used in development against SARS-CoV-2. Classical (conventional) include those that are based on vaccines already licensed and used in humans. The next generation vaccines do not require the actual viral particle and can be developed solely on the sequence of the antigenic viral proteins.

Theranostics Image (Click on the image to enlarge.)

Simultaneously, according to the data obtained from the World Health Organization database up to 155 candidate vaccines are recently in preclinical tests [41]. Among these are 55 protein subunit candidates, 19 RNA, 19 non-replicating viral vector vaccines, 17 replicating viral vector vaccines, 15 VLP, 13 DNA candidates, 12 inactivated, 3 containing live attenuated virus, and two others (Figure 2A & B).

Currently, both classic vaccine platforms and next-generation vaccine platforms can be distinguished (Figure 4). Classic (conventional) include those that are based on vaccines already licensed and used in humans. These vaccines are either virus-based or protein-based. Virus-based vaccines may contain live attenuated virus or inactivated virus. Vaccines contained live attenuated viruses are created by multiple passages of the virus in cell culture, leading to its loss of virulence. This type of vaccines leads to the development of a mild infection. Vaccines based on the inactivated virus ensure that the virion cannot replicate and is not contagious. However they do require adjuvants to properly stimulate the immune response. Protein-based vaccines may consist of a virus-purified protein, a recombinant protein, or virus-like particles (VLP). Inactivated virus vaccines and protein-based vaccines require adjuvants to stimulate the immune system [42-45]. Virus-like particles contain the structural proteins of viral capsid. Simultaneously, they do not have the viral genome and critical non-structural proteins [46].

The next generation vaccines do not require the actual viral particle and can be developed solely on the sequence of the antigenic viral proteins. The material present in the vaccine containing information about the protein coding sequence leads to its biosynthesis and thus to an immune response. Next-generation vaccines include viral vector, nucleic acid-based and antigen-presenting cells vaccines [43,44,46]. Characteristics of selected vaccines are presented in Table 2.

Classical vaccine platforms

Inactivated Vaccines

Inactivated vaccines belong to the classic strategy for viral vaccinations. These vaccines contain multiple antigenic components and therefore, can potentially induce diverse immunologic responses [22]. In comparison to live-attenuated vaccines, they reportedly have less reactogenicity and are typically characterized by weaker immune responses. Inactivated vaccines may require multiple inoculations and strong adjuvants to be effective. The advantages are, however, that development process is well established and streamlined but requires handling of the live virus [47]. At present the most advanced candidates are in phase 3 of the clinical trials, including the Sinovac vaccine (Sinovac Research and Development Co., Ltd./Butantan Institute), and the COVID-19 vaccine produced on Vero cells (Wuhan Institute of Biological Products Co., Ltd./Sinopharm/Beijing Institute of Biological Products Co., Ltd.). One candidate is in Phase 2 (Shenzhen Kangtai Biological Products Co., Ltd.; Beijing Minhai Biotechnology Co., Ltd.). Three other candidates are still in phase 1/2 of the clinical trials such as BBV152 (Bharat Biotech International Limited), QazCovid-in (Research Institute for Biological Safety Problems) and SARS-CoV-2 vaccine from the Chinese Academy of Medical Sciences. In preclinical evaluation are 12 inactivated candidates.

Live-Attenuated Vaccines

Live-attenuated vaccines also belong to the classic strategy for viral vaccinations and contain multiple antigenic components [22]. The advantage of whole-virus vaccines is strong immunogenicity and stimulation of Toll-like receptors. The protection is usually long-lasting as shown by examples of vaccines against smallpox, poliovirus and measles. Their effectiveness is confirmed, among others by eradication of smallpox and very close to successful eradication of polio diseases [48]. The development process is well established but also requires handling of live virus particles during production [47]. In immunocompromised persons, live vaccines can theoretically lead to development of fully-fledged infection. Therefore, they must have additional tests to confirm their safety [49]. At present there are no live-attenuated vaccines in clinical stages. Three live-attenuated vaccines are in preclinical evaluation, developed by Mehmet Ali Aydinlar University, Codagenix/Serum Institute of India and Indian Immunologicals Ltd/Griffith University [41].

Subunit Vaccines

Subunit vaccines contain one or more antigens with strong immunogenicity. They are safer and less difficult to manufacture because they do not require handling of live virus particles during the production process. Their disadvantage is that this type of vaccine often requires effective adjuvants to obtain stronger immune responses [22]. In general, subunit vaccines consisted of immunogenic proteins, which have properties of immunoprotective antigens. They are safer than immunization with all inactivated pathogen [50]. The first group of the SARS-CoV-2 subunit vaccines uses the S protein as antigens. Examples of such vaccines are SCB-2019 vaccine (Clover Biopharmaceuticals AUS Pty Ltd.), NVX-CoV2373 (Novavax), Covax-19 (GeneCure Biotechnologies; Vaxine Pty Ltd.), the vaccine developed by University of Queensland and MVC-COV1901 (Medigen Vaccine Biologics Corp.). The second group are subunit vaccines employing the RBD domain of S protein as antigen: KBP-COVID-19 (Kentucky BioProcessing, Inc.) and vaccine from Anhui Zhifei Longcom Biologic Pharmacy Co., Ltd. Vaccine NVX-CoV2373 (Novavax) is currently in phase 3, and others subunit vaccines against SARS-CoV-2 are in phase 1 or 2 of clinical trials. In preclinical evaluation are 55 protein subunit candidates.

In studies of NVX-CoV2373 vaccine, 83 and 25 participants received the vaccine with adjuvant and without adjuvant, respectively. In most persons, local and systemic reactogenicity was absent or mild. The most often adverse effects reported were headache, fatigue, and malaise. There have been no presented severe adverse events. In adjuvant-based trials enhanced immune responses and induction of T helper 1 (Th1) cells was demonstrated. Moreover, two doses of adjuvant vaccine induced production of anti-spike IgG with neutralization responses. Anti-spike IgG levels were approximately 100 times higher than in patients with symptomatic Covid-19 [51].

Virus-like particles vaccines (VLP)

VLP vaccines contain many viral structural proteins and mimic the organization and conformation of viruses. These vaccines do not contain the viral genome and therefore are non-infectious and very safe. The use of a combination of structural proteins from different viruses produces recombinant VLPs [52,53].

Of particular interest are vaccines produced in plants. The plant cells are ideal platforms for the production of oral delivery vaccines. They are also commonly referred to as edible vaccines [54]. The genes for viral proteins are most commonly introduced to host plant using pathogenic bacteria Agrobacterium. After infection, the gene of interest incorporates into nuclear or chloroplast genome. This transformation leads to biosynthesis of very large amounts of virus-like particles in the plant host [55]. It was shown that plant vaccines manufactured using Agrobacterium infiltration-based transient expression platform (Nicotiana benthamiana) against avian influenza H5 (AIV) pandemic and influenza A viruses (A/H1N1, A/H3N2) were safe and well-tolerated. Moreover, it was confirmed as inducing strong and cross-reactive humoral and cellular responses [56]. This type of vaccine was shown a promising source of the vaccine of Newcastle disease [57], of Lyme disease [58], a glycoprotein of bovine viral diarrhea virus [59], and recombinant colicin M [60]. Among candidates against SARS-CoV-2 are also RBD SARS-CoV-2 HBsAg VLP vaccine in Phase 1/2 (Serum Institute of India), and plant-derived coronavirus-VLP vaccine (Medicago), that recently entered phase 1 trials. In preclinical evaluation are 15 VLP candidates.

Next-generation vaccine platforms

Viral Vector-Based Vaccines

Live vector-based vaccines are live recombinant viruses, which deliver vaccine genes or antigens to the target host tissues. Attenuation is essential for safety; however, despite this vector-based vaccines have an elevated risk of certain adverse events (Table 2). The viral vector imitates infection caused by genuine virus. Therefore it can induce stronger cellular immune response than recombinant protein vaccine [47]. There is currently a number of non-replicating vaccines in development based on both adenoviral and lentiviral vectors. The adenoviral-vectored includes being in Phase 3 ChAdOx1 nCoV-19/AZD1222 (University of Oxford/Astra Zeneca; University of Witwatersrand, South Africa), Ad26.COV2.S (Janssen Vaccines & Prevention B.V.), Ad5-nCoV (Insitute of Biotechnology, Academy of Military Medical Sciences, PLA of China/CanSino Biologics Inc.) and Gam-COVID-Vac (Gamaleya Research Institute of Epidemiology and Microbiology, Health Ministry of the Russian Federation). Moreover, 2019-nCOV candidate (Institute of Biotechnology, Academy of Military Medical Sciences, PLA of China) is in Phase 2, and three vaccines: VXA-CoV2-1 (Vaxart), hAd5-S-Fusion+N-ETSD (ImmunityBio, Inc.) and defective Simian adenovirus vectored GRAd-COV2 (ReiThera Srl) are in Phase 1. Lentiviral vector-based vaccines in development include currently the LV-SMENP-DC in Phase 1/2 and Pathogen-specific aAPC vaccine in Phase 1, both tested by Shenzhen Geno-Immune Medical Institute.

In Phase 1/2 of clinical trials is replicating VSV vectored rVSV-SARS-CoV-2-S/IIBR-100 vaccine (Israel Institute for Biological Research), and in Phase 1 are also four replicating viral vectored vaccines (Table 1), it is intranasal flu vectored DelNS1-2019-nCoV-RBD-OPT1 (Beijing Wantai Biological Pharmacy), measles-vector based TMV-083 (Institut Pasteur/Themis Bioscience/Coalition for Epidemic Preparedness Innovations), VSV-vector based V590 (Merck Sharp & Dohme Corp.), and modified vaccinia virus Ankara vectored MVA-SARS-2-S (Universitätsklinikum Hamburg-Eppendorf). In preclinical evaluation are currently 19 non-replicating and 17 replicating candidates.

In a preliminary report of a phase 1/2, a single-blind, randomized controlled trial the ChAdOx1 nCoV-19 was shown an acceptable safety profile. Authors did not observe any serious adverse effects related to ChAdOx1 nCoV-19. Spike-specific T-cell responses peaked on day 14 post inoculation. Neutralizing antibody responses against SARS-CoV-2 were also detected in more than 90% of participants [61].

Good tolerability and immunogenicity were also reported for recombinant adenovirus type-5 (Ad5) vectored vaccine, currently in phase 1 trial. Among 108 participants neutralizing antibodies increased significantly on day 14 and peaked 28 days post-vaccination. After administration of a single dose of the vaccine, a four-fold increase in the number of RBD-binding antibodies was found in up to 100% of participants, and of neutralizing antibodies in up to 75% of participants. However, most of the individuals exhibited adverse side effects such as pain at the injection site, fever, fatigue, headache, and muscle pain. No serious and systemic side effects were reported so far [62]. In the phase 2 trial, two doses of the Ad5-vectored vaccine induced significant neutralizing antibody responses to live coronavirus. Severe adverse reactions were reported in about 10% of participants. No serious adverse effects were documented [63].

In Russian studies it was shown that Gam-COVID-Vac vaccine was safe and well tolerated by 76 participants. The adverse events were mild and most common were pain at injection site, fever, headache, asthenia, and muscle and joint pain. After 21 days, in all subjects production of antibodies against SARS-CoV-2 glycoprotein was observed. Formation of T-helper (CD4+) and T-killer (CD8+) cells was confirmed in all participants at day 28 [64].

mRNA Vaccines

mRNA vaccines are characterized by high potency what is connected with adjuvant. They have short production cycles and potential for rapid and low-cost manufacturing [65]. These vaccines induce activation of both B cell responses and T cell cytotoxicity [66]. In some mRNA vaccines, lipid nanoparticles (LNPs) are used to enhance the mRNA transfection efficacy [67]. One vaccine mRNA-1273 (Moderna TX, Inc./National Institute of Allergy and Infectious Diseases) is currently in Phase 3 of clinical trials and one BNT162 (BioNTech/Fosun Pharma/Pfizer) in Phase 2/3. CVnCoV (CureVac AG) is in Phase 2 and ARCT-021 (Arcturus Therapeutics, Inc.) in Phase 1/2. The other two vaccines, LNP-nCoVsaRNA (Imperial College London) and vaccine from Yunnan Walvax Biotechnology Co., Ltd, are currently in Phase 1 of clinical trials. In preclinical evaluation are 19 RNA candidates.

The mRNA-1273 vaccine consists of a mRNA drug surrounded by lipid nanoparticles (LNPs). It was recently observed that immunization with mRNA-1273 vaccine induced strong SARS-CoV-2 neutralizing activity in non-human primates [68]. In phase 1 trials, it has been also demonstrated that the mRNA-1273 vaccine was effective in eliciting immune responses in all tested 45 participants when used in two injections 28 days apart. Side effects included predominantly pain and inflammation at the injection site, fatigue, chills, headache, and myalgia. Systemic adverse effects after the first vaccination were reported as mild to moderate, but were more severe and frequent after the second vaccination [69].

DNA Vaccines

DNA vaccines mainly contain plasmid DNA that encodes one or more antigens. They need to enter the nucleus for the production of antigen proteins to take place [70]. This type of vaccine eliminates the need for using live viruses and are amenable for freeze-drying and long-term storage [47]. So far, four SARS-CoV-2 DNA vaccines are under development including INO-4800 (International Vaccine Institute; Inovio Pharmaceuticals), nCov vaccine (Cadila Healthcare Ltd.), AG0301-COVID19 (AnGes, Inc.) and GX-19 (Genexine, Inc.). All of these candidates are in Phase 1/2 of clinical trials. In preclinical evaluation are currently 13 DNA candidate vaccines.

Challenges with accelerated vaccine development

It has been shown that candidate vaccines lead to production of antibodies against SARS-CoV-2 [51,61,62]. However, it is unknown how long immunity will last after vaccination. Antibody titers in persons after SARS-CoV-1 or MERS-CoV infections often weakened after 1-3 years [71,72]. Studies in rhesus macaques showed that anti-S-IgG antibodies did not inhibit SARS-CoV infection, but instead exacerbated macrophage-mediated lung damage [73]. In persons with COVID-19, it was shown that antibodies can be undetectable three months after infection [74]. Today we know, that both neutralizing antibodies and cellular immune responses are important in responding to SARS-CoV-2, and potential vaccines should elicit both of these responses [75,76]. Some case reports presented that in patients is possible reinfection with SARS-CoV-2 [77,78]. Unfortunately, in some persons, second infection can be harder than first, which may indicate a short time of persistence of antibodies after primary infection. It is also possible, as in Denga virus, occurrence of antibody-dependent enhancement (ADE) leading to exacerbation of COVID-19 by anti-SARS-CoV-2 antibodies [79].

According to Logunov et al., the COVID-19 vector vaccine candidates were well tolerated and did not cause serious adverse events during phase 1 and 2 studies [64]. However, according to observation during other trials [61-63], after vaccination against SARS-CoV-2 may occur side effects including injection site pain, fever, fatigue, headache, muscle pain, diarrhoea, nausea, appetite impaired, swelling, and cough. At present, phase 3 studies are underway for the Moderna and BioNTech/Pfizer vaccines, the Oxford/AstraZeneca viral vector vaccine and the Johnson & Johnson viral vector vaccine, enrolling 30,000-40,000 subjects [80]. However, at last scientists urge caution in global vaccine race because the next phase of clinical trials is hold after “suspected adverse event” (the inflammation of spinal cord) in a person who received the vaccine in the UK [80,81].

The main purpose of vaccination is to eliminate or significantly reduce disease transmission in a population by inducing herd immunity. The herd immunity in healthy persons is obtained in case of influenza after vaccination of above 80% of population [82], and in case of measles more than 90% [83]. It is estimated that 67% of the population are required to be vaccinated to obtain herd immunity to SARS-CoV-2 [84]. This would require production of over 5 billion doses of one-dose vaccine or more than 10 billion of double-doses vaccine. The challenge will be also production and distribution of vials to store the vaccines and syringes to administer them.

Until outbreak of current pandemic, the development of vaccines and their approval lasted on average more than 15 years [85]. Vaccines against SARS-CoV-1 have not been introduced for 17 years since the outbreak of the epidemic and MERS-CoV for 6 years. Therefore, in recent pandemic the timing of the first vaccine implementation is unknown, but due to social and economic costs the pressure for rapid development and implementation is immense. There are advantages and disadvantages to each vaccine platforms. No DNA or RNA vaccine is currently licensed and approved for therapeutic use in humans. Viral vector vaccines exhibit potential risk such as chromosomal integration and oncogenesis, and generally cannot be used in immunocompromised subjects. Protein vaccines need adjuvants to enhance immunological response. At the same time global scale deployment of attenuated vaccines is always associated with risks of pathogen reactivation and regaining its virulence in the future [86]. At present every vaccine technology represents a compromise between good efficacy, safety, and a lack of side-effects.

Future outlook

Development and dissemination of vaccines has been one of the great achievements of contemporary medicine. However, despite benefits, their clinical use carries also some risks. It should be remembered that e.g. the influenza virus changes its antigenic structure. Within each type and subtype of seasonal influenza virus, new major antigenic variants arise approximately every 3-8 years [87]. Even if we manage to develop and deploy a COVID-19 vaccine the main uncertainty lies in how mutations of the SARS-CoV-2 strains will affect its effectiveness. According to Mercatelli and Giorgi [88], the SARS-CoV-2 virus has at least six identified strains and its variability is not high. This means that the vaccines under development can be potentially effective against major strains of the virus [88].

Global efforts are continuing to attempt to inhibit and eradicate of the COVID-19 pandemic. The unprecedented race towards effective and suitable candidates for SARS-CoV-2 vaccines is ongoing. The most advanced so far are eight very different vaccines that just entered phase 3 trials. The results obtained in clinical trials so far are promising, but more research is required on the efficacy and safety of these vaccines. However, the development and introduction of a vaccine for use is a multi-stage and long-term process. In addition, the production and distribution of a huge number of vaccine doses will be a problem. Ultimately, even if a vaccine becomes available, it will take many years to get herd immunity in human society.


Author contributions

TMK and MO contributed to the conception and design of the work. TMK, MO, AS-M, HW and DW analyzed data and wrote the manuscript. TMK, MO and DW revised and approved the manuscript. TMK performed the figures and tables.

Competing Interests

The authors have declared that no competing interest exists.


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Corresponding address Corresponding author: E-mail:

Received 2020-9-24
Accepted 2020-11-8
Published 2021-1-1