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SARS-CoV-2 variant B.1.1.7 is susceptible to neutralizing antibodies elicited by ancestral spike vaccines

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...

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Autores principales: Shen, Xiaoying, Tang, Haili, McDanal, Charlene, Wagh, Kshitij, Fischer, William, Theiler, James, Yoon, Hyejin, Li, Dapeng, Haynes, Barton F., Sanders, Kevin O., Gnanakaran, Sandrasegaram, Hengartner, Nick, Pajon, Rolando, Smith, Gale, Glenn, Gregory M., Korber, Bette, Montefiori, David C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934674/
https://www.ncbi.nlm.nih.gov/pubmed/33705729
http://dx.doi.org/10.1016/j.chom.2021.03.002
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author Shen, Xiaoying
Tang, Haili
McDanal, Charlene
Wagh, Kshitij
Fischer, William
Theiler, James
Yoon, Hyejin
Li, Dapeng
Haynes, Barton F.
Sanders, Kevin O.
Gnanakaran, Sandrasegaram
Hengartner, Nick
Pajon, Rolando
Smith, Gale
Glenn, Gregory M.
Korber, Bette
Montefiori, David C.
author_facet Shen, Xiaoying
Tang, Haili
McDanal, Charlene
Wagh, Kshitij
Fischer, William
Theiler, James
Yoon, Hyejin
Li, Dapeng
Haynes, Barton F.
Sanders, Kevin O.
Gnanakaran, Sandrasegaram
Hengartner, Nick
Pajon, Rolando
Smith, Gale
Glenn, Gregory M.
Korber, Bette
Montefiori, David C.
author_sort Shen, Xiaoying
collection PubMed
description 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.
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spelling pubmed-79346742021-03-05 SARS-CoV-2 variant B.1.1.7 is susceptible to neutralizing antibodies elicited by ancestral spike vaccines Shen, Xiaoying Tang, Haili McDanal, Charlene Wagh, Kshitij Fischer, William Theiler, James Yoon, Hyejin Li, Dapeng Haynes, Barton F. Sanders, Kevin O. Gnanakaran, Sandrasegaram Hengartner, Nick Pajon, Rolando Smith, Gale Glenn, Gregory M. Korber, Bette Montefiori, David C. Cell Host Microbe Short Article 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. Elsevier Inc. 2021-04-14 2021-03-05 /pmc/articles/PMC7934674/ /pubmed/33705729 http://dx.doi.org/10.1016/j.chom.2021.03.002 Text en © 2021 Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Short Article
Shen, Xiaoying
Tang, Haili
McDanal, Charlene
Wagh, Kshitij
Fischer, William
Theiler, James
Yoon, Hyejin
Li, Dapeng
Haynes, Barton F.
Sanders, Kevin O.
Gnanakaran, Sandrasegaram
Hengartner, Nick
Pajon, Rolando
Smith, Gale
Glenn, Gregory M.
Korber, Bette
Montefiori, David C.
SARS-CoV-2 variant B.1.1.7 is susceptible to neutralizing antibodies elicited by ancestral spike vaccines
title SARS-CoV-2 variant B.1.1.7 is susceptible to neutralizing antibodies elicited by ancestral spike vaccines
title_full SARS-CoV-2 variant B.1.1.7 is susceptible to neutralizing antibodies elicited by ancestral spike vaccines
title_fullStr SARS-CoV-2 variant B.1.1.7 is susceptible to neutralizing antibodies elicited by ancestral spike vaccines
title_full_unstemmed SARS-CoV-2 variant B.1.1.7 is susceptible to neutralizing antibodies elicited by ancestral spike vaccines
title_short SARS-CoV-2 variant B.1.1.7 is susceptible to neutralizing antibodies elicited by ancestral spike vaccines
title_sort sars-cov-2 variant b.1.1.7 is susceptible to neutralizing antibodies elicited by ancestral spike vaccines
topic Short Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934674/
https://www.ncbi.nlm.nih.gov/pubmed/33705729
http://dx.doi.org/10.1016/j.chom.2021.03.002
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