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接种疫苗后针对关注变异株的新冠病毒T细胞免疫

SARS -CoV-2 T-cell immunity to variants of concern following vaccination.

作者信息

Gallagher Kathleen M E, Leick Mark B, Larson Rebecca C, Berger Trisha R, Katsis Katelin, Yam Jennifer Y, Brini Gabrielle, Grauwet Korneel, Maus Marcela V

机构信息

Immune Monitoring Laboratory, Cancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.

Cellular Immunotherapy Program, Cancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.

出版信息

bioRxiv. 2021 May 3:2021.05.03.442455. doi: 10.1101/2021.05.03.442455.

Abstract

Recently, two mRNA vaccines to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have become available, but there is also an emergence of SARS-CoV-2 variants with increased transmissibility and virulence. A major concern is whether the available vaccines will be equally effective against these variants. The vaccines are designed to induce an immune response against the SARS-CoV-2 spike protein, which is required for viral entry to host cells. Immunity to SARS-CoV-2 is often evaluated by antibody production, while less is known about the T-cell response. Here we developed, characterized, and implemented two standardized, functional assays to measure T-cell immunity to SARS-CoV-2 in uninfected, convalescent, and vaccinated individuals. We found that vaccinated individuals had robust T-cell responses to the wild type spike and nucleocapsid proteins, even more so than convalescent patients. We also found detectable but diminished T-cell responses to spike variants (B.1.1.7, B.1.351, and B.1.1.248) among vaccinated but otherwise healthy donors. Since decreases in antibody neutralization have also been observed with some variants, investigation into the T-cell response to these variants as an alternative means of viral control is imperative. Standardized measurements of T-cell responses to SARS-CoV-2 are feasible and can be easily adjusted to determine changes in response to variants.

摘要

最近,两种针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的mRNA疫苗已可供使用,但同时也出现了传播性和毒性增加的SARS-CoV-2变体。一个主要担忧是现有的疫苗对这些变体是否同样有效。这些疫苗旨在诱导针对SARS-CoV-2刺突蛋白的免疫反应,而该蛋白是病毒进入宿主细胞所必需的。对SARS-CoV-2的免疫力通常通过抗体产生来评估,而对T细胞反应的了解则较少。在此,我们开发、表征并实施了两种标准化的功能测定方法,以测量未感染、康复和接种疫苗个体对SARS-CoV-2的T细胞免疫力。我们发现,接种疫苗的个体对野生型刺突蛋白和核衣壳蛋白有强烈的T细胞反应,甚至比康复患者更强烈。我们还发现,在接种疫苗但其他方面健康的供体中,对刺突变体(B.1.1.7、B.1.351和B.1.1.248)的T细胞反应可检测到但有所减弱。由于在一些变体中也观察到抗体中和作用的下降,因此必须将对这些变体的T细胞反应作为一种替代的病毒控制手段进行研究。对SARS-CoV-2的T细胞反应进行标准化测量是可行的,并且可以很容易地进行调整以确定对变体反应的变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/096f/8109204/6072c1fac30a/nihpp-2021.05.03.442455-f0005.jpg

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