用于 SARS-CoV-2 预防和免疫疗法的人类中和抗体。

IF 4.1 Q2 IMMUNOLOGY
Immunotherapy advances Pub Date : 2021-12-30 eCollection Date: 2022-01-01 DOI:10.1093/immadv/ltab027
Dongyan Zhou, Runhong Zhou, Zhiwei Chen
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引用次数: 0

摘要

严重急性呼吸系统综合征冠状病毒-2(SARS-CoV-2)是冠状病毒病 2019(COVID-19)的病原体。自 2019 年 12 月以来,SARS-CoV-2 一直在全球范围内传播,导致 COVID-19 持续大流行,截至 2021 年 10 月 11 日,感染人数达 2.37 亿,死亡人数达 480 万。虽然全球在疫苗接种方面做出了巨大努力,但结束这场大流行仍面临着病毒传染性极高、再感染、疫苗突破感染和免疫逃逸变异等问题的挑战。除了破纪录的疫苗研发速度,包括 SARS-CoV-2 特异性人类中和抗体(HuNAbs)在内的抗病毒药物也被积极探索用于被动免疫。为了支持以 HuNAb 为基础的免疫疗法,使用康复患者血浆进行被动免疫已取得了对轻度和重度 COVID-19 患者均有临床疗效的可喜证据。由于康复患者血浆的来源有限,广谱反应性 HuNAb 的发现可能会对抗击 COVID-19 大流行产生重大影响。因此,在本综述中,我们将讨论目前的基因克隆技术、作用模式、体外和体内效力和广度以及强效 SARS-CoV-2 特异性 HuNAbs 的临床开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Human neutralizing antibodies for SARS-CoV-2 prevention and immunotherapy.

Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is the causative agent of coronavirus disease 2019 (COVID-19). SARS-CoV-2 has been spreading worldwide since December 2019, resulting in the ongoing COVID-19 pandemic with 237 million infections and 4.8 million deaths by 11 October 2021. While there are great efforts of global vaccination, ending this pandemic has been challenged by issues of exceptionally high viral transmissibility, re-infection, vaccine-breakthrough infection, and immune escape variants of concern. Besides the record-breaking speed of vaccine research and development, antiviral drugs including SARS-CoV-2-specific human neutralizing antibodies (HuNAbs) have been actively explored for passive immunization. In support of HuNAb-based immunotherapy, passive immunization using convalescent patients' plasma has generated promising evidence on clinical benefits for both mild and severe COVID-19 patients. Since the source of convalescent plasma is limited, the discovery of broadly reactive HuNAbs may have significant impacts on the fight against the COVID-19 pandemic. In this review, therefore, we discuss the current technologies of gene cloning, modes of action, in vitro and in vivo potency and breadth, and clinical development for potent SARS-CoV-2-specific HuNAbs.

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