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一种强效、广谱中和的人源单克隆抗体,可有效保护 hACE2 转基因小鼠免受武汉、BA.5 和 XBB.1.5 等 SARS-CoV-2 变异株的感染。

A potent, broadly neutralizing human monoclonal antibody that efficiently protects hACE2-transgenic mice from infection with the Wuhan, BA.5, and XBB.1.5 SARS-CoV-2 variants.

机构信息

Institute of Molecular and Cellular Biology, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.

Department of Vaccinology, Smorodintsev Research Institute of Influenza, Saint Petersburg, Russia.

出版信息

Front Immunol. 2024 Jul 19;15:1442160. doi: 10.3389/fimmu.2024.1442160. eCollection 2024.

Abstract

The COVID-19 pandemic has uncovered the high genetic variability of the SARS-CoV-2 virus and its ability to evade the immune responses that were induced by earlier viral variants. Only a few monoclonal antibodies that have been reported to date are capable of neutralizing a broad spectrum of SARS-CoV-2 variants. Here, we report the isolation of a new broadly neutralizing human monoclonal antibody, iC1. The antibody was identified through sorting the SARS-CoV-1 RBD-stained individual B cells that were isolated from the blood of a vaccinated donor following a breakthrough infection. , iC1 potently neutralizes pseudoviruses expressing a wide range of SARS-CoV-2 Spike variants, including those of the XBB sublineage. In an hACE2-transgenic mouse model, iC1 provided effective protection against the Wuhan strain of the virus as well as the BA.5 and XBB.1.5 variants. Therefore, iC1 can be considered as a potential component of the broadly neutralizing antibody cocktails resisting the SARS-CoV-2 mutation escape.

摘要

COVID-19 大流行揭示了 SARS-CoV-2 病毒的高遗传变异性及其逃避早期病毒变异诱导的免疫反应的能力。迄今为止,只有少数几种已报道的单克隆抗体能够中和广谱的 SARS-CoV-2 变体。在这里,我们报告了一种新的广泛中和的人源单克隆抗体 iC1 的分离。该抗体是通过对从接种疫苗的供体突破性感染后血液中分离的 SARS-CoV-1 RBD 染色的个体 B 细胞进行分选而鉴定出来的。iC1 能够有效地中和表达广泛 SARS-CoV-2 Spike 变体的假病毒,包括 XBB 亚系的变体。在 hACE2 转基因小鼠模型中,iC1 对武汉株病毒以及 BA.5 和 XBB.1.5 变体提供了有效保护。因此,iC1 可以被认为是抵抗 SARS-CoV-2 突变逃逸的广泛中和抗体鸡尾酒的潜在成分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3c5/11294225/98edb055cc2e/fimmu-15-1442160-g001.jpg

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