Literature DB >> 23507469

CD19+CD5+ B cells and B1-like cells following allogeneic hematopoietic stem cell transplantation.

Hélène Moins-Teisserenc1, Marc Busson, Adel Herda, Sandrine Apete, Regis Peffault de Latour, Marie Robin, Aliénor Xhaard, Antoine Toubert, Gérard Socié.   

Abstract

We and others have previously reported the expansion of CD5(+)CD19(+) B cells after allogeneic hematopoietic stem cell transplantation. Recently, the equivalent of B1 cells in mice has been described in humans as CD20(+)CD27(+)CD43(+)CD70(-) B cells. In this article, we report that although 39% of CD5(+)CD19(+) cells were CD43(+) in controls, >75% of CD5(+)CD19(+) cells were CD43(+) in patients independent of the presence or absence of chronic graft-versus-host disease (GVHD) (P = .0001). CD5(+)CD19(+) B cell, CD5(+)CD43(+)CD19(+) B cell, and CD27(+)CD43(+) B cell counts were significantly lower in the patients with previous chronic GVHD, and this effect of GVHD was similar in both CD5(+) and CD5(-) within the CD27(+)CD43(+) B cell subset. Our results strongly suggest that the previously reported expansion of the CD5(+)CD19(+) population might be related to an expansion of the CD27(+)CD43(+) B cell subset and that CD27(+)CD43(+) B cell reconstitution is impaired in patients with chronic GVHD.
Copyright © 2013 American Society for Blood and Marrow Transplantation. Published by Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23507469     DOI: 10.1016/j.bbmt.2013.03.006

Source DB:  PubMed          Journal:  Biol Blood Marrow Transplant        ISSN: 1083-8791            Impact factor:   5.742


  18 in total

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2.  Cytomegalovirus shapes long-term immune reconstitution after allogeneic stem cell transplantation.

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Review 10.  Translating transitions - how to decipher peripheral human B cell development.

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