在SARS-CoV-2中和抗体反应中频繁使用IGHV3-30-3。

IF 2 Q4 VIROLOGY Frontiers in virology Pub Date : 2023-03-01 DOI:10.3389/fviro.2023.1128253
Pradeepa Pushparaj, Andrea Nicoletto, Xaquin Castro Dopico, Daniel J Sheward, Sungyong Kim, Simon Ekström, Ben Murrell, Martin Corcoran, Gunilla B Karlsson Hedestam
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摘要

对SARS-CoV-2的抗体反应显示有偏倚的免疫球蛋白重链变量(IGHV)基因使用,允许定义某些类别的中和抗体的遗传特征。我们通过在大流行早期从SARS-CoV-2感染者中分选刺特异性单记忆B细胞来调查IGHV基因的使用频率。从两名研究参与者和703个尖刺特异性B细胞中,最常用的基因是IGHV1-69、IGHV3-30-3和IGHV3-30。在这里,我们重点研究了IGHV3-30组基因和使用超强中和单克隆抗体CAB-F52的IGHV3-30-3,该单克隆抗体在其种系恢复形式中也显示出广泛的中和活性。IGHV3-30-3是由IGH位点的一个区域编码的,该区域在等位基因和结构水平上都是高度可变的。通过个性化IG基因分型,我们发现14名研究参与者中有4人在两条染色体上都缺乏IGHV3-30-3基因,这就提出了一个问题,即其他高度相似的IGHV基因是否可以替代缺乏该基因的人的IGHV3-30-3。在CAB-F52的背景下,我们发现所有测试的IGHV3-33等位基因都不能替代IGHV3-30-3,但有几个IGHV3-30等位基因可以替代IGHV3-30-3,这表明该抗体高度同源的IGHV3-30和IGHV3-30-3基因之间存在功能冗余。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Frequent use of IGHV3-30-3 in SARS-CoV-2 neutralizing antibody responses.

The antibody response to SARS-CoV-2 shows biased immunoglobulin heavy chain variable (IGHV) gene usage, allowing definition of genetic signatures for some classes of neutralizing antibodies. We investigated IGHV gene usage frequencies by sorting spike-specific single memory B cells from individuals infected with SARS-CoV-2 early in the pandemic. From two study participants and 703 spikespecific B cells, the most used genes were IGHV1-69, IGHV3-30-3, and IGHV3-30. Here, we focused on the IGHV3-30 group of genes and an IGHV3-30-3-using ultrapotent neutralizing monoclonal antibody, CAB-F52, which displayed broad neutralizing activity also in its germline-reverted form. IGHV3-30-3 is encoded by a region of the IGH locus that is highly variable at both the allelic and structural levels. Using personalized IG genotyping, we found that 4 of 14 study participants lacked the IGHV3-30-3 gene on both chromosomes, raising the question if other, highly similar IGHV genes could substitute for IGHV3-30-3 in persons lacking this gene. In the context of CAB-F52, we found that none of the tested IGHV3-33 alleles, but several IGHV3-30 alleles could substitute for IGHV3-30-3, suggesting functional redundancy between the highly homologous IGHV3-30 and IGHV3-30-3 genes for this antibody.

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