Literature DB >> 31732168

Liver Is a Generative Site for the B Cell Response to Ehrlichia muris.

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.
Copyright © 2019 Elsevier Inc. All rights reserved.

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


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