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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors.
2022
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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. |
format | Online Article Text |
id | pubmed-8801307 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Authors. |
record_format | MEDLINE/PubMed |
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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