Broadly neutralizing antibodies against COVID-19

IF 5.7 2区 医学 Q1 VIROLOGY Current opinion in virology Pub Date : 2023-08-01 DOI:10.1016/j.coviro.2023.101332
Daming Zhou , Jingshan Ren , Elizabeth E Fry , David I Stuart
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引用次数: 4

Abstract

The COVID-19 pandemic caused by SARS-CoV-2 has led to hundreds of millions of infections and millions of deaths, however, human monoclonal antibodies (mAbs) can be an effective treatment. Since SARS-CoV-2 emerged, a variety of strains have acquired increasing numbers of mutations to gain increased transmissibility and escape from the immune response. Most reported neutralizing human mAbs, including all approved therapeutic ones, have been knocked down or out by these mutations. Broadly neutralizing mAbs are therefore of great value, to treat current and possible future variants. Here, we review four types of neutralizing mAbs against the spike protein with broad potency against previously and currently circulating variants. These mAbs target the receptor-binding domain, the subdomain 1, the stem helix, or the fusion peptide. Understanding how these mAbs retain potency in the face of mutational change could guide future development of therapeutic antibodies and vaccines.

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广泛中和抗COVID-19抗体
由SARS-CoV-2引起的新冠肺炎大流行已导致数亿人感染和数百万人死亡,然而,人类单克隆抗体(mAbs)可能是一种有效的治疗方法。自严重急性呼吸系统综合征冠状病毒2型出现以来,各种毒株获得了越来越多的突变,以增加传播性并逃避免疫反应。大多数报道的中和性人类单克隆抗体,包括所有批准的治疗性单克隆抗体,都已被这些突变击倒或淘汰。因此,广泛中和的单克隆抗体对治疗当前和未来可能的变体具有巨大价值。在这里,我们回顾了四种针对刺突蛋白的中和单克隆抗体,它们对以前和现在流行的变体具有广泛的效力。这些mAb靶向受体结合结构域、亚结构域1、干螺旋或融合肽。了解这些单克隆抗体在面对突变变化时如何保持效力,可以指导未来治疗性抗体和疫苗的开发。
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来源期刊
CiteScore
11.80
自引率
5.10%
发文量
76
审稿时长
83 days
期刊介绍: Current Opinion in Virology (COVIRO) is a systematic review journal that aims to provide specialists with a unique and educational platform to keep up to date with the expanding volume of information published in the field of virology. It publishes 6 issues per year covering the following 11 sections, each of which is reviewed once a year: Emerging viruses: interspecies transmission; Viral immunology; Viral pathogenesis; Preventive and therapeutic vaccines; Antiviral strategies; Virus structure and expression; Animal models for viral diseases; Engineering for viral resistance; Viruses and cancer; Virus vector interactions. There is also a section that changes every year to reflect hot topics in the field.
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