Cargando…
B.1.526 SARS-CoV-2 Variants Identified in New York City are Neutralized by Vaccine-Elicited and Therapeutic Monoclonal Antibodies
DNA sequence analysis recently identified the novel SARS-CoV-2 variant B.1.526 that is spreading at an alarming rate in the New York City area. Two versions of the variant were identified, both with the prevalent D614G mutation in the spike protein, together with four novel point mutations and with...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406170/ https://www.ncbi.nlm.nih.gov/pubmed/34311587 http://dx.doi.org/10.1128/mBio.01386-21 |
_version_ | 1783746468790665216 |
---|---|
author | Zhou, Hao Dcosta, Belinda M. Samanovic, Marie I. Mulligan, Mark J. Landau, Nathaniel R. Tada, Takuya |
author_facet | Zhou, Hao Dcosta, Belinda M. Samanovic, Marie I. Mulligan, Mark J. Landau, Nathaniel R. Tada, Takuya |
author_sort | Zhou, Hao |
collection | PubMed |
description | DNA sequence analysis recently identified the novel SARS-CoV-2 variant B.1.526 that is spreading at an alarming rate in the New York City area. Two versions of the variant were identified, both with the prevalent D614G mutation in the spike protein, together with four novel point mutations and with an E484K or S477N mutation in the receptor-binding domain, raising concerns of possible resistance to vaccine-elicited and therapeutic antibodies. We report that convalescent-phase sera and vaccine-elicited antibodies retain full neutralizing titer against the S477N B.1.526 variant and neutralize the E484K version with a modest 3.5-fold decrease in titer compared to D614G. The E484K version was neutralized with a 12-fold decrease in titer by the REGN10933 monoclonal antibody, but the combination cocktail with REGN10987 was fully active. The findings suggest that current vaccines and Regeneron therapeutic monoclonal antibodies will remain protective against the B.1.526 variants. The findings further support the value of widespread vaccination. |
format | Online Article Text |
id | pubmed-8406170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-84061702021-09-09 B.1.526 SARS-CoV-2 Variants Identified in New York City are Neutralized by Vaccine-Elicited and Therapeutic Monoclonal Antibodies Zhou, Hao Dcosta, Belinda M. Samanovic, Marie I. Mulligan, Mark J. Landau, Nathaniel R. Tada, Takuya mBio Observation DNA sequence analysis recently identified the novel SARS-CoV-2 variant B.1.526 that is spreading at an alarming rate in the New York City area. Two versions of the variant were identified, both with the prevalent D614G mutation in the spike protein, together with four novel point mutations and with an E484K or S477N mutation in the receptor-binding domain, raising concerns of possible resistance to vaccine-elicited and therapeutic antibodies. We report that convalescent-phase sera and vaccine-elicited antibodies retain full neutralizing titer against the S477N B.1.526 variant and neutralize the E484K version with a modest 3.5-fold decrease in titer compared to D614G. The E484K version was neutralized with a 12-fold decrease in titer by the REGN10933 monoclonal antibody, but the combination cocktail with REGN10987 was fully active. The findings suggest that current vaccines and Regeneron therapeutic monoclonal antibodies will remain protective against the B.1.526 variants. The findings further support the value of widespread vaccination. American Society for Microbiology 2021-07-27 /pmc/articles/PMC8406170/ /pubmed/34311587 http://dx.doi.org/10.1128/mBio.01386-21 Text en Copyright © 2021 Zhou et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Observation Zhou, Hao Dcosta, Belinda M. Samanovic, Marie I. Mulligan, Mark J. Landau, Nathaniel R. Tada, Takuya B.1.526 SARS-CoV-2 Variants Identified in New York City are Neutralized by Vaccine-Elicited and Therapeutic Monoclonal Antibodies |
title | B.1.526 SARS-CoV-2 Variants Identified in New York City are Neutralized by Vaccine-Elicited and Therapeutic Monoclonal Antibodies |
title_full | B.1.526 SARS-CoV-2 Variants Identified in New York City are Neutralized by Vaccine-Elicited and Therapeutic Monoclonal Antibodies |
title_fullStr | B.1.526 SARS-CoV-2 Variants Identified in New York City are Neutralized by Vaccine-Elicited and Therapeutic Monoclonal Antibodies |
title_full_unstemmed | B.1.526 SARS-CoV-2 Variants Identified in New York City are Neutralized by Vaccine-Elicited and Therapeutic Monoclonal Antibodies |
title_short | B.1.526 SARS-CoV-2 Variants Identified in New York City are Neutralized by Vaccine-Elicited and Therapeutic Monoclonal Antibodies |
title_sort | b.1.526 sars-cov-2 variants identified in new york city are neutralized by vaccine-elicited and therapeutic monoclonal antibodies |
topic | Observation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406170/ https://www.ncbi.nlm.nih.gov/pubmed/34311587 http://dx.doi.org/10.1128/mBio.01386-21 |
work_keys_str_mv | AT zhouhao b1526sarscov2variantsidentifiedinnewyorkcityareneutralizedbyvaccineelicitedandtherapeuticmonoclonalantibodies AT dcostabelindam b1526sarscov2variantsidentifiedinnewyorkcityareneutralizedbyvaccineelicitedandtherapeuticmonoclonalantibodies AT samanovicmariei b1526sarscov2variantsidentifiedinnewyorkcityareneutralizedbyvaccineelicitedandtherapeuticmonoclonalantibodies AT mulliganmarkj b1526sarscov2variantsidentifiedinnewyorkcityareneutralizedbyvaccineelicitedandtherapeuticmonoclonalantibodies AT landaunathanielr b1526sarscov2variantsidentifiedinnewyorkcityareneutralizedbyvaccineelicitedandtherapeuticmonoclonalantibodies AT tadatakuya b1526sarscov2variantsidentifiedinnewyorkcityareneutralizedbyvaccineelicitedandtherapeuticmonoclonalantibodies |