The effect of SARS-CoV-2 D614G mutation on BNT162b2 vaccine-elicited neutralization
Abstract Initial COVID-19 vaccine candidates were based on the original sequence of SARS-CoV-2. However, the virus has since accumulated mutations, among which the spike D614G is dominant in circulating virus, raising questions about potential virus escape from vaccine-elicited immunity. Here, we re...
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Nature Portfolio
2021
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oai:doaj.org-article:ec866784239c40d8b7031906e2ca75862021-12-02T14:02:53ZThe effect of SARS-CoV-2 D614G mutation on BNT162b2 vaccine-elicited neutralization10.1038/s41541-021-00313-82059-0105https://doaj.org/article/ec866784239c40d8b7031906e2ca75862021-03-01T00:00:00Zhttps://doi.org/10.1038/s41541-021-00313-8https://doaj.org/toc/2059-0105Abstract Initial COVID-19 vaccine candidates were based on the original sequence of SARS-CoV-2. However, the virus has since accumulated mutations, among which the spike D614G is dominant in circulating virus, raising questions about potential virus escape from vaccine-elicited immunity. Here, we report that the D614G mutation modestly reduced (1.7–2.4-fold) SARS-CoV-2 neutralization by BNT162b2 vaccine-elicited mouse, rhesus, and human sera, concurring with the 95% vaccine efficacy observed in clinical trial.Jing ZouXuping XieCamila R. Fontes-GarfiasKena A. SwansonIsis KanevskyKristin TompkinsMark CutlerDavid CooperPhilip R. DormitzerPei-Yong ShiNature PortfolioarticleImmunologic diseases. AllergyRC581-607Neoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENnpj Vaccines, Vol 6, Iss 1, Pp 1-4 (2021) |
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Immunologic diseases. Allergy RC581-607 Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 |
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Immunologic diseases. Allergy RC581-607 Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 Jing Zou Xuping Xie Camila R. Fontes-Garfias Kena A. Swanson Isis Kanevsky Kristin Tompkins Mark Cutler David Cooper Philip R. Dormitzer Pei-Yong Shi The effect of SARS-CoV-2 D614G mutation on BNT162b2 vaccine-elicited neutralization |
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Abstract Initial COVID-19 vaccine candidates were based on the original sequence of SARS-CoV-2. However, the virus has since accumulated mutations, among which the spike D614G is dominant in circulating virus, raising questions about potential virus escape from vaccine-elicited immunity. Here, we report that the D614G mutation modestly reduced (1.7–2.4-fold) SARS-CoV-2 neutralization by BNT162b2 vaccine-elicited mouse, rhesus, and human sera, concurring with the 95% vaccine efficacy observed in clinical trial. |
format |
article |
author |
Jing Zou Xuping Xie Camila R. Fontes-Garfias Kena A. Swanson Isis Kanevsky Kristin Tompkins Mark Cutler David Cooper Philip R. Dormitzer Pei-Yong Shi |
author_facet |
Jing Zou Xuping Xie Camila R. Fontes-Garfias Kena A. Swanson Isis Kanevsky Kristin Tompkins Mark Cutler David Cooper Philip R. Dormitzer Pei-Yong Shi |
author_sort |
Jing Zou |
title |
The effect of SARS-CoV-2 D614G mutation on BNT162b2 vaccine-elicited neutralization |
title_short |
The effect of SARS-CoV-2 D614G mutation on BNT162b2 vaccine-elicited neutralization |
title_full |
The effect of SARS-CoV-2 D614G mutation on BNT162b2 vaccine-elicited neutralization |
title_fullStr |
The effect of SARS-CoV-2 D614G mutation on BNT162b2 vaccine-elicited neutralization |
title_full_unstemmed |
The effect of SARS-CoV-2 D614G mutation on BNT162b2 vaccine-elicited neutralization |
title_sort |
effect of sars-cov-2 d614g mutation on bnt162b2 vaccine-elicited neutralization |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/ec866784239c40d8b7031906e2ca7586 |
work_keys_str_mv |
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