| Literature DB >> 28694183 |
Evelyn C Nieves1, Tomomi Toubai1, Daniel C Peltier2, Katherine Oravecz-Wilson1, Chen Liu3, Hiroya Tamaki4, Yaping Sun1, Pavan Reddy5.
Abstract
Professional antigen-presenting cells (APCs) are important modulators of acute graft-versus-host disease (GVHD). Although dendritic cells (DCs) are the most potent APC subset, other myeloid cells, especially macrophages (MFs) and neutrophils, recently have been shown to play a role in the severity of GVHD. The critical molecular mechanisms that determine the functions of myeloid cells in GVHD are unclear, however. Signal transducer and activator of transcription 3 (STAT3) is a master transcription factor that plays a crucial role in regulating immunity, but its role in MF biology and in acute GVHD remains unknown. To determine the impact of myeloid cell-specific expression of STAT3 on the severity of acute GVHD, we used myeloid cell-specific STAT3-deficient LysM-Cre/STAT3fl/- animals as recipients and donors in well-characterized experimental models of acute GVHD. We found that reduced expression of STAT3 in myeloid cells from the hosts, but not the donors, increased inflammation, increased donor T cell activation, and exacerbated GVHD. Our data demonstrate that STAT3 in host myeloid cells, such as MFs, dampens acute GVHD.Entities:
Keywords: Bone marrow transplantation; Graft-versus-host disease; Myeloid cells; STAT-3
Mesh:
Substances:
Year: 2017 PMID: 28694183 PMCID: PMC6088768 DOI: 10.1016/j.bbmt.2017.06.018
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742