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BNT162b2 诱导的针对 B.1.617 和其他 SARS-CoV-2 变体的中和作用。

BNT162b2-elicited neutralization of B.1.617 and other SARS-CoV-2 variants.

机构信息

Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.

Institute for Human Infections and Immunity, University of Texas Medical Branch, Galveston, TX, USA.

出版信息

Nature. 2021 Aug;596(7871):273-275. doi: 10.1038/s41586-021-03693-y. Epub 2021 Jun 10.

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is continuing to evolve around the world, generating new variants that are of concern on the basis of their potential for altered transmissibility, pathogenicity, and coverage by vaccines and therapeutic agents. Here we show that serum samples taken from twenty human volunteers, two or four weeks after their second dose of the BNT162b2 vaccine, neutralize engineered SARS-CoV-2 with a USA-WA1/2020 genetic background (a virus strain isolated in January 2020) and spike glycoproteins from the recently identified B.1.617.1, B.1.617.2, B.1.618 (all of which were first identified in India) or B.1.525 (first identified in Nigeria) lineages. Geometric mean plaque reduction neutralization titres against the variant viruses-particularly the B.1.617.1 variant-seemed to be lower than the titre against the USA-WA1/2020 virus, but all sera tested neutralized the variant viruses at titres of at least 1:40. The susceptibility of the variant strains to neutralization elicited by the BNT162b2 vaccine supports mass immunization as a central strategy to end the coronavirus disease 2019 (COVID-19) pandemic globally.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)在全球范围内持续进化,产生了新的变种,这些变种基于其潜在的传染性、致病性和疫苗及治疗药物的覆盖范围而令人担忧。在这里,我们展示了从二十名人类志愿者采集的血清样本,这些志愿者在接种 BNT162b2 疫苗的第二剂后两到四周,能够中和具有美国 WA1/2020 遗传背景(2020 年 1 月分离出的病毒株)和最近发现的 B.1.617.1、B.1.617.2、B.1.618(均在印度首次发现)或 B.1.525(首次在尼日利亚发现)谱系的刺突糖蛋白的工程 SARS-CoV-2。针对变体病毒的几何平均噬斑减少中和滴度(尤其是针对 B.1.617.1 变体)似乎低于针对美国 WA1/2020 病毒的滴度,但所有测试的血清都能以至少 1:40 的滴度中和变体病毒。变异株对 BNT162b2 疫苗引发的中和作用的敏感性支持大规模免疫接种,这是在全球范围内结束 2019 冠状病毒病(COVID-19)大流行的核心策略。

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