| Literature DB >> 26179902 |
Jun Long1, Li Chang1, Yan Shen2, Wen-Hui Gao1, Yue-Nv Wu1, Han-Bo Dou1, Meng-Meng Huang1, Ying Wang1, Wei-Yue Fang1, Jie-Hui Shan1, Yue-Ying Wang3, Jiang Zhu3, Zhu Chen3, Jiong Hu4.
Abstract
Graft-versus-host disease (GVHD) is the major complication after allogeneic bone marrow transplantation. Valproic acid (VPA) was described as a histone deacetylase inhibitor that had anti-inflammatory effects and reduced the production of proinflammatory cytokines in experimental autoimmune disease models. Using well-characterized mouse models of MHC-mismatched transplantation, we studied the effects of VPA on GVHD severity and graft-versus-leukemia (GVL) activity. Administration of VPA significantly attenuated the clinical severity of GVHD, the histopathology of GVHD-involved organs, and the overall mortality from GVHD. VPA downregulated Th1 and Th17 cell responses and cytokine production in vitro and in vivo, whereas its effect on GVHD was regulatory T cell independent. The effect of VPA was related to its ability to directly reduce the activity of Akt, an important regulator of T cell immune responses. Importantly, when mice received lethal doses of host-type acute leukemia cells, administration of VPA did not impair GVL activity and resulted in significantly improved leukemia-free survival. These findings reveal a unique role for VPA as a histone deacetylase inhibitor in reducing the donor CD4(+) T cells that contribute to GVHD, which may provide a strategy to reduce GVHD while preserving the GVL effect.Entities:
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Year: 2015 PMID: 26179902 DOI: 10.4049/jimmunol.1500578
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422