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SARS-CoV-2 variant B.1.1.7 is susceptible to neutralizing antibodies elicited by ancestral spike vaccines.
- Source :
-
Cell host & microbe [Cell Host Microbe] 2021 Apr 14; Vol. 29 (4), pp. 529-539.e3. Date of Electronic Publication: 2021 Mar 05. - Publication Year :
- 2021
-
Abstract
- All current vaccines for COVID-19 utilize ancestral SARS-CoV-2 spike with the goal of generating protective neutralizing antibodies. The recent emergence and rapid spread of several SARS-CoV-2 variants carrying multiple spike mutations raise concerns about possible immune escape. One variant, first identified in the United Kingdom (B.1.1.7, also called 20I/501Y.V1), contains eight spike mutations with potential to impact antibody therapy, vaccine efficacy, and risk of reinfection. Here, we show that B.1.1.7 remains sensitive to neutralization, albeit at moderately reduced levels (∼sim;2-fold), by serum samples from convalescent individuals and recipients of an mRNA vaccine (mRNA-1273, Moderna) and a protein nanoparticle vaccine (NVX-CoV2373, Novavax). A subset of monoclonal antibodies to the receptor binding domain (RBD) of spike are less effective against the variant, while others are largely unaffected. These findings indicate that variant B.1.1.7 is unlikely to be a major concern for current vaccines or for an increased risk of reinfection.<br />Competing Interests: Declaration of interests R.P. is an employee of Moderna, Inc. G.S. and G.M.G. are employees of Novavax, Inc.<br /> (Copyright © 2021 Elsevier Inc. All rights reserved.)
- Subjects :
- 2019-nCoV Vaccine mRNA-1273
Adolescent
Adult
Aged
Aged, 80 and over
Antibodies, Monoclonal immunology
Female
Humans
Male
Middle Aged
Mutation
Neutralization Tests
Spike Glycoprotein, Coronavirus genetics
Spike Glycoprotein, Coronavirus immunology
Young Adult
Antibodies, Neutralizing immunology
Antibodies, Viral immunology
COVID-19 Vaccines immunology
SARS-CoV-2 immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1934-6069
- Volume :
- 29
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Cell host & microbe
- Publication Type :
- Academic Journal
- Accession number :
- 33705729
- Full Text :
- https://doi.org/10.1016/j.chom.2021.03.002