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Long-term, infection-acquired immunity against the SARS-CoV-2 Delta variant in a hamster model

The emergence of the SARS-CoV-2 Delta variant (B.1.617.2) raises concerns about potential reduced sensitivity of the virus to antibody neutralization and subsequent vaccine breakthrough infections. Here, we use a live virus neutralization assay with sera from Pfizer- and Moderna-vaccinated individua...

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Autores principales: Halfmann, Peter J., Kuroda, Makoto, Armbrust, Tammy, Accola, Molly, Valdez, Riccardo, Kowalski-Dobson, Theresa, Rehrauer, William, Gordon, Aubree, Kawaoka, Yoshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8801307/
https://www.ncbi.nlm.nih.gov/pubmed/35139368
http://dx.doi.org/10.1016/j.celrep.2022.110394
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author Halfmann, Peter J.
Kuroda, Makoto
Armbrust, Tammy
Accola, Molly
Valdez, Riccardo
Kowalski-Dobson, Theresa
Rehrauer, William
Gordon, Aubree
Kawaoka, Yoshihiro
author_facet Halfmann, Peter J.
Kuroda, Makoto
Armbrust, Tammy
Accola, Molly
Valdez, Riccardo
Kowalski-Dobson, Theresa
Rehrauer, William
Gordon, Aubree
Kawaoka, Yoshihiro
author_sort Halfmann, Peter J.
collection PubMed
description The emergence of the SARS-CoV-2 Delta variant (B.1.617.2) raises concerns about potential reduced sensitivity of the virus to antibody neutralization and subsequent vaccine breakthrough infections. Here, we use a live virus neutralization assay with sera from Pfizer- and Moderna-vaccinated individuals to examine neutralizing antibody titers against SARS-CoV-2 and observe a 3.9- and 2.7-fold reduction, respectively, in neutralizing antibody titers against the Delta variant compared with an early isolate bearing only a D614G substitution in its spike protein. We observe similar reduced sensitivity with sera from hamsters that were previously infected with an early isolate of SARS-CoV-2. Despite this reduction in neutralizing antibody titers against the Delta variant, hamsters previously infected (up to 15 months earlier) with an early isolate are protected from infection with the Delta variant, suggesting that the immune response to the first infection is sufficient to provide protection against subsequent infection with the Delta variant.
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spelling pubmed-88013072022-01-31 Long-term, infection-acquired immunity against the SARS-CoV-2 Delta variant in a hamster model Halfmann, Peter J. Kuroda, Makoto Armbrust, Tammy Accola, Molly Valdez, Riccardo Kowalski-Dobson, Theresa Rehrauer, William Gordon, Aubree Kawaoka, Yoshihiro Cell Rep Report The emergence of the SARS-CoV-2 Delta variant (B.1.617.2) raises concerns about potential reduced sensitivity of the virus to antibody neutralization and subsequent vaccine breakthrough infections. Here, we use a live virus neutralization assay with sera from Pfizer- and Moderna-vaccinated individuals to examine neutralizing antibody titers against SARS-CoV-2 and observe a 3.9- and 2.7-fold reduction, respectively, in neutralizing antibody titers against the Delta variant compared with an early isolate bearing only a D614G substitution in its spike protein. We observe similar reduced sensitivity with sera from hamsters that were previously infected with an early isolate of SARS-CoV-2. Despite this reduction in neutralizing antibody titers against the Delta variant, hamsters previously infected (up to 15 months earlier) with an early isolate are protected from infection with the Delta variant, suggesting that the immune response to the first infection is sufficient to provide protection against subsequent infection with the Delta variant. The Authors. 2022-02-15 2022-01-31 /pmc/articles/PMC8801307/ /pubmed/35139368 http://dx.doi.org/10.1016/j.celrep.2022.110394 Text en © 2022 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
Halfmann, Peter J.
Kuroda, Makoto
Armbrust, Tammy
Accola, Molly
Valdez, Riccardo
Kowalski-Dobson, Theresa
Rehrauer, William
Gordon, Aubree
Kawaoka, Yoshihiro
Long-term, infection-acquired immunity against the SARS-CoV-2 Delta variant in a hamster model
title Long-term, infection-acquired immunity against the SARS-CoV-2 Delta variant in a hamster model
title_full Long-term, infection-acquired immunity against the SARS-CoV-2 Delta variant in a hamster model
title_fullStr Long-term, infection-acquired immunity against the SARS-CoV-2 Delta variant in a hamster model
title_full_unstemmed Long-term, infection-acquired immunity against the SARS-CoV-2 Delta variant in a hamster model
title_short Long-term, infection-acquired immunity against the SARS-CoV-2 Delta variant in a hamster model
title_sort long-term, infection-acquired immunity against the sars-cov-2 delta variant in a hamster model
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8801307/
https://www.ncbi.nlm.nih.gov/pubmed/35139368
http://dx.doi.org/10.1016/j.celrep.2022.110394
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