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SARS-CoV-2 重组受体结合域(RBD)诱导针对 SARS-CoV-2 和 SARS-CoV-1 变异株的中和抗体。

SARS-COV-2 recombinant Receptor-Binding-Domain (RBD) induces neutralizing antibodies against variant strains of SARS-CoV-2 and SARS-CoV-1.

机构信息

Department of Medical Microbiology & Immunology, University of Alberta, Edmonton, Canada; Li Ka Shing Institute of Virology, University of Alberta, Edmonton, Canada.

Department of Medical Microbiology & Immunology, University of Alberta, Edmonton, Canada; Li Ka Shing Institute of Virology, University of Alberta, Edmonton, Canada.

出版信息

Vaccine. 2021 Sep 24;39(40):5769-5779. doi: 10.1016/j.vaccine.2021.08.081. Epub 2021 Aug 26.

Abstract

SARS-CoV-2 is the etiological agent of COVID19. There are currently several licensed vaccines approved for human use and most of them target the spike protein in the virion envelope to induce protective immunity. Recently, variants that spread more quickly have emerged. There is evidence that some of these variants are less sensitive to neutralization in vitro, but it is not clear whether they can evade vaccine induced protection. In this study, we tested SARS-CoV-2 spike RBD as a vaccine antigen and explored the effect of formulation with Alum/MPLA or AddaS03 adjuvants. Our results show that RBD induces high titers of neutralizing antibodies and activates strong cellular immune responses. There is also significant cross-neutralization of variants B.1.1.7 and B.1.351 and to a lesser extent, SARS-CoV-1. These results indicate that recombinant RBD can be a viable candidate as a stand-alone vaccine or as a booster shot to diversify our strategy for COVID19 protection.

摘要

SARS-CoV-2 是 COVID19 的病原体。目前已有几种获得许可的人类使用疫苗,其中大多数针对病毒包膜中的刺突蛋白,以诱导保护性免疫。最近,出现了传播速度更快的变体。有证据表明,其中一些变体在体外对中和作用的敏感性较低,但尚不清楚它们是否能够逃避疫苗诱导的保护。在这项研究中,我们测试了 SARS-CoV-2 刺突 RBD 作为疫苗抗原,并探索了与 Alum/MPLA 或 AddaS03 佐剂联合使用的效果。我们的结果表明,RBD 诱导高滴度的中和抗体,并激活强烈的细胞免疫反应。对变体 B.1.1.7 和 B.1.351 以及在较小程度上对 SARS-CoV-1 也有显著的交叉中和作用。这些结果表明,重组 RBD 可以作为一种可行的候选物,作为单一疫苗或作为加强针,多样化我们预防 COVID19 的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abe/8387217/14d9db4e80e2/gr1_lrg.jpg

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