| Literature DB >> 31732168 |
Nikita Trivedi1, Florian Weisel2, Shuchi Smita3, Stephen Joachim2, Muhamuda Kader4, Aditya Radhakrishnan5, Chris Clouser5, Aaron M Rosenfeld6, Maria Chikina7, Francois Vigneault5, Uri Hershberg6, Nahed Ismail4, Mark Jay Shlomchik8.
Abstract
The B cell response to Ehrlichia muris is dominated by plasmablasts (PBs), with few-if any-germinal centers (GCs), yet it generates protective immunoglobulin M (IgM) memory B cells (MBCs) that express the transcription factor T-bet and harbor V-region mutations. Because Ehrlichia prominently infects the liver, we investigated the nature of liver B cell response and that of the spleen. B cells within infected livers proliferated and underwent somatic hypermutation (SHM). Vh-region sequencing revealed trafficking of clones between the spleen and liver and often subsequent local clonal expansion and intraparenchymal localization of T-bet+ MBCs. T-bet+ MBCs expressed MBC subset markers CD80 and PD-L2. Many T-bet+ MBCs lacked CD11b or CD11c expression but had marginal zone (MZ) B cell phenotypes and colonized the splenic MZ, revealing T-bet+ MBC plasticity. Hence, liver and spleen are generative sites of B cell responses, and they include V-region mutation and result in liver MBC localization.Entities:
Keywords: Ehrlichia muris; T-bet; age-associated B cells; liver; memory B cells; plasmablasts; somatic hypermutation
Mesh:
Substances:
Year: 2019 PMID: 31732168 PMCID: PMC6955021 DOI: 10.1016/j.immuni.2019.10.004
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745