| Literature DB >> 31375460 |
Jonathan A Roco1, Luka Mesin2, Sebastian C Binder3, Christian Nefzger4, Paula Gonzalez-Figueroa1, Pablo F Canete1, Julia Ellyard1, Qian Shen1, Philippe A Robert3, Jean Cappello1, Harpreet Vohra1, Yang Zhang5, Carla R Nowosad2, Arien Schiepers2, Lynn M Corcoran6, Kai-Michael Toellner5, Jose M Polo4, Michael Meyer-Hermann7, Gabriel D Victora2, Carola G Vinuesa8.
Abstract
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.Entities:
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Year: 2019 PMID: 31375460 PMCID: PMC6914312 DOI: 10.1016/j.immuni.2019.07.001
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745