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High-titer neutralization of Mu and C.1.2 SARS-CoV-2 variants by vaccine-elicited antibodies of previously infected individuals

Recently identified severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants Mu and C.1.2 have spike proteins with mutations that may confer resistance to natural and vaccine-elicited antibodies. Analysis of neutralizing antibody titers in the sera of vaccinated individuals without prev...

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Autores principales: Tada, Takuya, Zhou, Hao, Dcosta, Belinda M., Samanovic, Marie I., Cornelius, Amber, Herati, Ramin S., Mulligan, Mark J., Landau, Nathaniel R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8687746/
https://www.ncbi.nlm.nih.gov/pubmed/34982967
http://dx.doi.org/10.1016/j.celrep.2021.110237
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author Tada, Takuya
Zhou, Hao
Dcosta, Belinda M.
Samanovic, Marie I.
Cornelius, Amber
Herati, Ramin S.
Mulligan, Mark J.
Landau, Nathaniel R.
author_facet Tada, Takuya
Zhou, Hao
Dcosta, Belinda M.
Samanovic, Marie I.
Cornelius, Amber
Herati, Ramin S.
Mulligan, Mark J.
Landau, Nathaniel R.
author_sort Tada, Takuya
collection PubMed
description Recently identified severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants Mu and C.1.2 have spike proteins with mutations that may confer resistance to natural and vaccine-elicited antibodies. Analysis of neutralizing antibody titers in the sera of vaccinated individuals without previous history of infection and from convalescent individuals show partial resistance of the viruses. In contrast, sera from individuals with a previous history of SARS-CoV-2 infection who were subsequently vaccinated neutralize variants with titers 4- to 11-fold higher, providing a rationale for vaccination of individuals with previous infection. The heavily mutated C.1.2 spike is the most antibody neutralization-resistant spike to date; however, the avidity of C.1.2 spike protein for angiotensin-converting enzyme 2 (ACE2) is low. This finding suggests that the virus evolved to escape the humoral response but has a decrease in fitness, suggesting that it may cause milder disease or be less transmissible. It may be difficult for the spike protein to evolve to escape neutralizing antibodies while maintaining high affinity for ACE2.
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spelling pubmed-86877462021-12-21 High-titer neutralization of Mu and C.1.2 SARS-CoV-2 variants by vaccine-elicited antibodies of previously infected individuals Tada, Takuya Zhou, Hao Dcosta, Belinda M. Samanovic, Marie I. Cornelius, Amber Herati, Ramin S. Mulligan, Mark J. Landau, Nathaniel R. Cell Rep Report Recently identified severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants Mu and C.1.2 have spike proteins with mutations that may confer resistance to natural and vaccine-elicited antibodies. Analysis of neutralizing antibody titers in the sera of vaccinated individuals without previous history of infection and from convalescent individuals show partial resistance of the viruses. In contrast, sera from individuals with a previous history of SARS-CoV-2 infection who were subsequently vaccinated neutralize variants with titers 4- to 11-fold higher, providing a rationale for vaccination of individuals with previous infection. The heavily mutated C.1.2 spike is the most antibody neutralization-resistant spike to date; however, the avidity of C.1.2 spike protein for angiotensin-converting enzyme 2 (ACE2) is low. This finding suggests that the virus evolved to escape the humoral response but has a decrease in fitness, suggesting that it may cause milder disease or be less transmissible. It may be difficult for the spike protein to evolve to escape neutralizing antibodies while maintaining high affinity for ACE2. The Authors. 2022-01-11 2021-12-21 /pmc/articles/PMC8687746/ /pubmed/34982967 http://dx.doi.org/10.1016/j.celrep.2021.110237 Text en © 2021 The Authors 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 Report
Tada, Takuya
Zhou, Hao
Dcosta, Belinda M.
Samanovic, Marie I.
Cornelius, Amber
Herati, Ramin S.
Mulligan, Mark J.
Landau, Nathaniel R.
High-titer neutralization of Mu and C.1.2 SARS-CoV-2 variants by vaccine-elicited antibodies of previously infected individuals
title High-titer neutralization of Mu and C.1.2 SARS-CoV-2 variants by vaccine-elicited antibodies of previously infected individuals
title_full High-titer neutralization of Mu and C.1.2 SARS-CoV-2 variants by vaccine-elicited antibodies of previously infected individuals
title_fullStr High-titer neutralization of Mu and C.1.2 SARS-CoV-2 variants by vaccine-elicited antibodies of previously infected individuals
title_full_unstemmed High-titer neutralization of Mu and C.1.2 SARS-CoV-2 variants by vaccine-elicited antibodies of previously infected individuals
title_short High-titer neutralization of Mu and C.1.2 SARS-CoV-2 variants by vaccine-elicited antibodies of previously infected individuals
title_sort high-titer neutralization of mu and c.1.2 sars-cov-2 variants by vaccine-elicited antibodies of previously infected individuals
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8687746/
https://www.ncbi.nlm.nih.gov/pubmed/34982967
http://dx.doi.org/10.1016/j.celrep.2021.110237
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