Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1784618236355018752 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8687746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Authors. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT tadatakuya hightiterneutralizationofmuandc12sarscov2variantsbyvaccineelicitedantibodiesofpreviouslyinfectedindividuals AT zhouhao hightiterneutralizationofmuandc12sarscov2variantsbyvaccineelicitedantibodiesofpreviouslyinfectedindividuals AT dcostabelindam hightiterneutralizationofmuandc12sarscov2variantsbyvaccineelicitedantibodiesofpreviouslyinfectedindividuals AT samanovicmariei hightiterneutralizationofmuandc12sarscov2variantsbyvaccineelicitedantibodiesofpreviouslyinfectedindividuals AT corneliusamber hightiterneutralizationofmuandc12sarscov2variantsbyvaccineelicitedantibodiesofpreviouslyinfectedindividuals AT heratiramins hightiterneutralizationofmuandc12sarscov2variantsbyvaccineelicitedantibodiesofpreviouslyinfectedindividuals AT mulliganmarkj hightiterneutralizationofmuandc12sarscov2variantsbyvaccineelicitedantibodiesofpreviouslyinfectedindividuals AT landaunathanielr hightiterneutralizationofmuandc12sarscov2variantsbyvaccineelicitedantibodiesofpreviouslyinfectedindividuals |