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定义由 SARS-CoV-2 抗体靶向的变异耐药表位:全球联盟研究。

Defining variant-resistant epitopes targeted by SARS-CoV-2 antibodies: A global consortium study.

机构信息

Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, 9420 Athena Circle, La Jolla, CA 92037, USA.

Carterra, 825 N. 300 W. Ste C309, Salt Lake City, UT 84103, USA.

出版信息

Science. 2021 Oct 22;374(6566):472-478. doi: 10.1126/science.abh2315. Epub 2021 Sep 23.

Abstract

Antibody-based therapeutics and vaccines are essential to combat COVID-19 morbidity and mortality after severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Multiple mutations in SARS-CoV-2 that could impair antibody defenses propagated in human-to-human transmission and spillover or spillback events between humans and animals. To develop prevention and therapeutic strategies, we formed an international consortium to map the epitope landscape on the SARS-CoV-2 spike protein, defining and structurally illustrating seven receptor binding domain (RBD)–directed antibody communities with distinct footprints and competition profiles. Pseudovirion-based neutralization assays reveal spike mutations, individually and clustered together in variants, that affect antibody function among the communities. Key classes of RBD-targeted antibodies maintain neutralization activity against these emerging SARS-CoV-2 variants. These results provide a framework for selecting antibody treatment cocktails and understanding how viral variants might affect antibody therapeutic efficacy.

摘要

基于抗体的治疗药物和疫苗对于应对严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染后的发病率和死亡率至关重要。SARS-CoV-2 发生了多种突变,这些突变可能会削弱在人际传播和人类与动物之间溢出或回溢事件中产生的抗体防御。为了制定预防和治疗策略,我们成立了一个国际联盟来绘制 SARS-CoV-2 刺突蛋白上的表位图谱,确定并结构说明了七个受体结合域(RBD)指导的抗体群体,它们具有不同的足迹和竞争特征。基于假病毒的中和测定显示,刺突突变单独存在以及在变体中聚集在一起,会影响各群体中的抗体功能。针对 RBD 的关键抗体类别保持对这些新出现的 SARS-CoV-2 变体的中和活性。这些结果为选择抗体治疗鸡尾酒提供了框架,并阐明了病毒变体如何影响抗体治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91e7/10765609/72d3d964ce25/science.abh2315-f1.jpg

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