A human coronavirus evolves antigenically to escape antibody immunity
Open accessPreprint — published as 10.1371/journal.ppat.1009453
Abstract
There is intense interest in antibody immunity to coronaviruses. However, it is unknown if coronaviruses evolve to escape such immunity, and if so, how rapidly. Here we address this question by characterizing the historical evolution of human coronavirus 229E. We identify human sera from the 1980s and 1990s that have neutralizing titers against contemporaneous 229E that are comparable to the anti-SARS-CoV-2 titers induced by SARS-CoV-2 infection or vaccination. We test these sera against 229E strains isolated after sera collection, and find that neutralizing titers are lower against these “future” viruses. In some cases, sera that neutralize contemporaneous 229E viral strains with titers >1:100 do not detectably neutralize strains isolated 8–17 years later. The decreased neutralization of “future” viruses is due to antigenic evolution of the viral spike, especially in the receptor-binding domain. If these results extrapolate to other coronaviruses, then it may be advisable to periodically update SARS-CoV-2 vaccines.
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Other groups have reported comparable findings with vaccinee and convalescent plasma across various pseudotype and authentic virus assays.
“In addition, similar results have been reported by others using vaccinee and convalescent plasmas and a variety of different pseudotype and authentic virus assays15,31,45–49.”
From mRNA vaccine-elicited antibodies to SARS-CoV-2 and circulating variants (2021) · cites this paper as [49]
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- Authors
- Eguia, R., Crawford, K. H. D., Stevens-Ayers, T., Kelnhofer-Millevolte, L., Greninger, A. L., Englund, J. A., Boeckh, M. J., & Bloom, J. D.
- Affiliations
- Fred Hutch Cancer Center (US)
- University of Washington (US)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Bloom, Jesse D.
- ORCID
- Venue
- PLoS Pathogens
- Publisher
- openRxiv
- Published
- 2020-12-18
- Volume
- 17
- Issue
- 4
- Pages
- e1009453-e1009453
- ISSN
- 1553-7366 (ISSN-L)
- PMC
- PMC8031418
- OpenAlex
- W3144378969
- Cited by
- 258
- References
- 101
- Citations by year
- 2026: 7 · 2025: 21 · 2024: 11 · 2023: 33 · 2022: 69 · 2021: 103 · 2020: 2 · 2018: 1 · 2017: 1 · 2015: 1 · 2014: 3 · 2013: 1
- FWCI
- 17.09
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- PLoS Pathogens (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Howard Hughes Medical Institute
- Pfizer
- AstraZeneca
- GlaxoSmithKline
- Sanofi
- Fred Hutchinson Cancer Research Center
- Regeneron Pharmaceuticals
- Moderna
- National Institutes of Health
- Sanofi Pasteur
- National Institute of General Medical Sciences (T32GM007266)
- National Institute of Allergy and Infectious Diseases (R01AI127893, F30AI149928, R01AI141707)
- Topics
- Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Animal Virus Infections Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › vaccines and immunoinformatics approaches
- Keywords
- HCoV-229E, antigenic evolution, antibody escape, neutralizing antibodies, spike protein, receptor binding domain, coronavirus evolution
- MeSH terms
- SARS-CoV-2, Antibodies, Viral, Humans, Coronavirus 229E, Human, Immune Evasion, Antibodies, Neutralizing
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