Rapid COVID-19 vaccine development
Abstract
Finding the fastest pathway to vaccine availability includes the avoidance of safety pitfalls
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TH1 and TH2 cell responses support B cell activation and differentiation for antigen-specific antibody production and long-term memory development through germinal cell responses.
“TH1 and TH2 cell responses support B cell activation and differentiation for antigen-specific antibody production and long-term memory development through germinal cell responses34,35.”
From An Omicron-specific, self-amplifying mRNA booster vaccine for COVID-19: a phase 2/3 randomized trial (2024) · cites this paper as [34]
Cellular immune responses are protective in SARS-CoV-2 infection.
“Cellular immune responses are protective in SARS-CoV-2 infection”
From Safety and immunogenicity of the SARS-CoV-2 ARCoV mRNA vaccine in Chinese adults: a randomised, double-blind, placebo-controlled, phase 1 trial (2022) · cites this paper as [24]
T-helper-1-biased responses might reduce the risk of vaccine-associated antibody-dependent enhancement of virus replication or other adverse reactions.
“and T-helper-1-biased responses might reduce the risk of vaccine-associated antibody-dependent enhancement of virus replication or other adverse reactions.24”
From Safety and immunogenicity of the SARS-CoV-2 ARCoV mRNA vaccine in Chinese adults: a randomised, double-blind, placebo-controlled, phase 1 trial (2022) · cites this paper as [24]
Previous experience with veterinary coronavirus vaccines and animal models of SARS-CoV and MERS-CoV infection have raised safety concerns about the potential for vaccine-associated enhanced respiratory disease.
“Previous experience with veterinary coronavirus vaccines and animal models of SARS-CoV and MERS-CoV infection have raised safety concerns about the potential for vaccine-associated enhanced respiratory disease.”
From An mRNA Vaccine against SARS-CoV-2 — Preliminary Report (2020) · cites this paper as [31]
These events were associated either with macrophage-tropic coronaviruses susceptible to antibody-dependent enhancement of replication or with vaccine antigens that induced antibodies with poor neutralizing activity and Th2-biased responses.
“These events were associated either with macrophage-tropic coronaviruses susceptible to antibody-dependent enhancement of replication or with vaccine antigens that induced antibodies with poor neutralizing activity and Th2-biased responses.31”
From An mRNA Vaccine against SARS-CoV-2 — Preliminary Report (2020) · cites this paper as [31]
Preclinical trials showed MRT5500 induced a Th1-biased immune response in mice and non-human primates and prevented Th2-bias response which can induce vaccine-related enhanced respiratory disease (VAERD).
“Results of preclinical trials showed that MRT5500 induced a Th1-biased immune response in mice and non-human primates and prevented Th2-bias response which can induce vaccine-related enhanced respiratory disease (VAERD).433–435”
From Advances in COVID-19 mRNA vaccine development (2022) · cites this paper as [433]
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“31 Reducing the risk of vaccine-associated enhanced respiratory disease or antibody-dependent enhancement of replication involves induction of high-quality functional antibody responses and Th1-biased T-cell responses.”
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“An ideal COVID-19 vaccine is supposed to avoid induction of non-neutralizing antibody and Th2-biased cellular immune responses because of safety concerns (Graham, 2020).”
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“A large number of different vaccine strategies for SARS-CoV-2 are being simultaneously pursued by multiple pharmaceutical companies and laboratories around the world (Amanat and Krammer, 2020; Graham, 2020; Sempowski et al., 2020).”
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“T H 1 and T H 2 cell responses support B cell activation and differentiation for antigen-specific antibody production and long-term memory development through germinal cell responses 34,35 .”
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- Authors
- Graham, B. S.
- Affiliations
- National Institutes of Health (US)
- Corresponding author
- Graham, Barney S.
- ORCID
- Graham, Barney S.
- Venue
- Science
- Published
- 2020-05-29
- Volume
- 368
- Issue
- 6494
- Pages
- 945-946
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W3023230016
- Cited by
- 771
- References
- 16
- Citations by year
- 2026: 25 · 2025: 25 · 2024: 58 · 2023: 81 · 2022: 170 · 2021: 248 · 2020: 163 · 2018: 1
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › vaccines and immunoinformatics approaches
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Legal, Health, Environmental and COVID-19 Challenges
- Keywords
- COVID-19 vaccines, vaccine development, vaccine safety, vaccine availability, SARS-CoV-2
- MeSH terms
- Betacoronavirus, COVID-19, SARS-CoV-2, COVID-19 Vaccines, Animals, Antibodies, Viral, Disease Models, Animal, Humans, Pneumonia, Viral, T-Lymphocytes, Viral Vaccines, Virus Replication, Cytokines, Coronavirus Infections, Antibody-Dependent Enhancement, Antibodies, Neutralizing, Pandemics
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