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Antibodies elicited by mRNA-1273 vaccination bind more broadly to the receptor binding domain than do those from SARS-CoV-2 infection
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Abstract
Deep mutational scanning shows that the mRNA-1273 RBD-binding antibody response is less affected by single viral mutations than the infection response.
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“Furthermore, mRNA vaccines have recently been successfully used against COVID-19, validating the platform and showing that mRNA vaccines can prevent infectious diseases in the future (Greaney et al., 2021).”
From A novel Toxoplasma gondii TGGT1_316290 mRNA-LNP vaccine elicits protective immune response against toxoplasmosis in mice (2023) · cites this paper as Greaney et al., 2021
Experimental — accuracy not yet measuredIn the citing paper
“L452R has resulted in 3-fold to 10-fold reduced susceptibility to about one third of convalescent and vaccinee plasma samples”
From The biological and clinical significance of emerging SARS-CoV-2 variants (2021) · cites this paper as [164]
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“The levels of neutralizing mAbs elicited by the mRNA vaccines has been high and in most persons are likely to be maintained for many months above the levels required for protection against even the most resistant circulating variants 164,239,240 .”
From The biological and clinical significance of emerging SARS-CoV-2 variants (2021) · cites this paper as [164]
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Research works printed but not linked: 3
- Pfizer and BioNTech confirm high efficacy and no serious safety concerns through up to six months following second dose in updated topline analysis of landmark COVID-19 vaccine study; www.pfizer.com/news/press-release/press-release-detail/pfizer-and-biontech-confirm-high-efficacy-and-no-serious.
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B Cell Receptor Repertoire Kinetics after SARS-CoV-2 Infection and VaccinationPreprint
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El‐Baky, N. A., & Amara, A. A. A. F. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.903876 · Cited by 5
Intrinsic immunogenicity is a major determinant of type-specific responses in SARS-CoV-2 infections
Quirk, G., Schoenle, M. V., Peyton, K. L., Uhrlaub, J. L., Lau, B., Liang, C.-Y., Burgess, J. L., Ellingson, K., Beitel, S. C., Romine, J. K., et al. (2025) · Nature Immunology · doi:10.1038/s41590-025-02162-2 · Cited by 5
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mRNA delivery of mosaic-8 pan-sarbecovirus RBD vaccines elicits distinct antibody epitope signatures
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Dickson, A. M., Geerling, E., Stone, E. T., Hassert, M., Steffen, T. L., Makkena, T., Smither, M., Schwetye, K. E., Zhang, J., Georges, B., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1188392 · Cited by 3
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Identification of an Optimized Receptor-Binding Domain Subunit Vaccine against SARS-CoV-2
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SARS-CoV-2 Immunity: Review of Immune Response to Infection and Vaccination
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Deep mutational scanning of whole SARS-CoV-2 spike in an inverted infection systemPreprint
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Molecular basis of pathogenicity of the recently emerged FCoV-23 coronavirusPreprint
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Self-citationViral immunity: Basic mechanisms and therapeutic applications—a Keystone Symposia report
Cable, J., Balachandran, S., Daley‐Bauer, L. P., Rustagi, A., Antony, F., Frere, J. J., Strampe, J., Kedzierska, K., Cannon, J. L., McGargill, M. A., et al. (2023) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14960 · Cited by 1
Self-citation
Metadata
- Authors
- Greaney, A. J., Loes, A. N., Gentles, L. E., Crawford, K. H. D., Starr, T. N., Malone, K. D., Chu, H. Y., & Bloom, J. D.
- Affiliations
- University of Washington (US)
- Howard Hughes Medical Institute (US)
- Fred Hutch Cancer Center (US)
- Corresponding author
- Bloom, Jesse D.
- ORCID
- Venue
- Science Translational Medicine
- Published
- 2021-06-30
- Volume
- 13
- Issue
- 600
- ISSN
- 1946-6234 (ISSN-L)
- 1946-6242
- PMC
- PMC8369496
- OpenAlex
- W3169651048
- Cited by
- 244
- References
- 53
- Citations by year
- 2026: 11 · 2025: 23 · 2024: 29 · 2023: 52 · 2022: 79 · 2021: 49
- FWCI
- 16.63
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Science Translational Medicine (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- PubMed Central (submittedVersion, cc-by)
- Funders
- National Institutes of Health (UM1AI148373, UM1AI148576, UM1AI148684, NIH P51 OD011132, AI149644, R01AI127893, S10OD028685, T32AI083203, F30AI149928)
- National Institute of Allergy and Infectious Diseases (UM1AI148373, R01AI141707, R01AI127893, T32AI083203, F30AI149928, UM1AI148576, UM1AI148684, NIH AID AI149644)
- Howard Hughes Medical Institute
- ASCRS Research Foundation (R01AI141707, R01AI127893, T32AI083203, F30AI149928, INV-004949, INV-016575, S10OD028685, DRG-2381-19, RNA-1273, UM1AI148373, UM1AI148576, UM1AI148684, NIH P51 OD011132, NIH AID AI149644, HHSN272201500002C)
- Bill and Melinda Gates Foundation (INV-004949, INV-016575)
- Gates Foundation (INV-004949, INV-016575)
- Damon Runyon Cancer Research Foundation (DRG-2381-19)
- Department of Health and Human Services (HHSN272201500002C)
- 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
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Animal Virus Infections Studies
- Keywords
- SARS-CoV-2, mRNA-1273 vaccine, COVID-19 vaccination, natural infection, receptor binding domain, spike protein, neutralizing antibodies, epitope specificity, viral evolution, antigenic drift, deep mutational scanning, convalescent sera
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