| Literature DB >> 28405514 |
Yue Hu1, Gan-Lin He2, Xiang-Yu Zhao3, Xiao-Su Zhao3, Yu Wang3, Lan-Ping Xu3, Xiao-Hui Zhang3, Xue-Zhong Yu4, Kai-Yan Liu3, Ying-Jun Chang3, Xiao-Jun Huang5.
Abstract
Regulatory B cells (Bregs) are involved in the pathogenesis of graft-versus-host disease (GVHD). However, whether Bregs can alleviate acute GVHD without compromising graft-versus-leukemia (GVL) effects remains unclear. Here, we evaluated the role of Bregs in acute GVHD and GVL activity in both a mouse model and a clinical cohort study. In the acute GVHD mouse model, co-transplantation of Bregs prevents onset through inhibiting Th1 and Th17 differentiation and expanding regulatory T cells. In the GVL mouse model, Bregs contributed to the suppression of acute GVHD but had no adverse effect on GVL activity. In the clinical cohort study, a higher dose of Bregs in allografts was associated with a lower cumulative incidence of acute GVHD but not with increased risk of relapse. Our data demonstrate that Bregs can prevent acute GVHD and maintain GVL effects and suggest that Bregs have potential as a novel strategy for acute GVHD alleviation.Entities:
Keywords: Allogeneic stem cell transplantation; Th cells; graft-versus-host disease; graft-versus-leukemia effects; regulatory B cells
Year: 2017 PMID: 28405514 PMCID: PMC5384367 DOI: 10.1080/2162402X.2017.1284721
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110