免疫球蛋白类转换
生发中心
体细胞突变
生物
生殖系
B细胞
同型
重组
抗体
V(D)J复合
遗传学
体细胞
基因
单克隆抗体
作者
Jonathan A. Roco,Luka Mesin,Sebastian Binder,Christian M. Nefzger,Paula González-Figueroa,Pablo F. Cañete,Julia I. Ellyard,Qian Shen,Philippe A. Robert,Jean Cappello,Harpreet Vohra,Yang Zhang,Carla R. Nowosad,Ariën Schiepers,Lynn M. Corcoran,Kai‐Michael Toellner,José M. Polo,Michael Meyer‐Hermann,Gabriel D. Victora,Carola G. Vinuesa
出处
期刊:Immunity
[Elsevier]
日期:2019-08-01
卷期号:51 (2): 337-350.e7
被引量:307
标识
DOI:10.1016/j.immuni.2019.07.001
摘要
Class-switch recombination (CSR) is a DNA recombination process that replaces the immunoglobulin (Ig) constant region for the isotype that can best protect against the pathogen. Dysregulation of CSR can cause self-reactive BCRs and B cell lymphomas; understanding the timing and location of CSR is therefore important. Although CSR commences upon T cell priming, it is generally considered a hallmark of germinal centers (GCs). Here, we have used multiple approaches to show that CSR is triggered prior to differentiation into GC B cells or plasmablasts and is greatly diminished in GCs. Despite finding a small percentage of GC B cells expressing germline transcripts, phylogenetic trees of GC BCRs from secondary lymphoid organs revealed that the vast majority of CSR events occurred prior to the onset of somatic hypermutation. As such, we have demonstrated the existence of IgM-dominated GCs, which are unlikely to occur under the assumption of ongoing switching.
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