| Literature DB >> 25015640 |
Yanwen Peng1, Xiaoyong Chen1, Qifa Liu1, Dijing Xu1, Haiqing Zheng1, Longshan Liu1, Qiuli Liu1, Muyun Liu1, Zhiping Fan1, Jing Sun1, Xiaobo Li1, Ruifeng Zou1, Andy Peng Xiang2.
Abstract
Although mesenchymal stromal cells (MSCs) possess immunomodulatory properties and exhibit promising efficacy against chronic graft-versus-host disease (cGVHD), little is known about the immune changes by which MSCs ameliorate cGVHD in vivo. Recent studies have suggested that B lymphocytes might play an important role in the pathogenesis of cGVHD. In this study, we investigated changes in the numbers, phenotypes, and subpopulations of B lymphocytes in cGVHD patients who showed a complete response (CR), partial response (PR), or no response (NR) after MSC treatment. We found that the frequencies and numbers of CD27+ memory and pre-germinal center B lymphocytes were significantly increased in the CR and PR cGVHD patients after MSC treatment but decreased in the NR patients. A further analysis of CR/PR cGVHD patients showed that MSC treatment led to a decrease in the plasma levels of B cell-activating factor (BAFF) and increased expression of the BAFF receptor (BAFF-R) on peripheral B lymphocytes but no changes in plasma BAFF levels or BAFF-R expression on B lymphocytes in NR patients. Overall, our findings imply that MSCs might exert therapeutic effects in cGVHD patients, accompanied by alteration of naïve and memory B-cell subsets, modulating plasma BAFF levels and BAFF-R expression on B lymphocytes. ©AlphaMed Press.Entities:
Keywords: B cell-activating factor; B-cell homeostasis; Chronic graft-versus-host disease; Mesenchymal stromal cells
Mesh:
Year: 2014 PMID: 25015640 PMCID: PMC4149298 DOI: 10.5966/sctm.2014-0001
Source DB: PubMed Journal: Stem Cells Transl Med ISSN: 2157-6564 Impact factor: 6.940