| Journal of Leukocyte Biology | |
| Donor- but not host-derived interleukin-10 contributes to the regulation of experimental graft-versus-host disease | |
| Evelyn Nieves2  Mariem Alrubaie2  Nathan Mathewson2  Hiroya Tamaki and2  Chen Liu1  Tomomi Toubai2  Rebecca Evers2  Isao Tawara2  Pavan Reddy2  Yaping Sun2  | |
| [1] Department of Pathology, University of Florida College of Medicine, Gainesville, Florida, USA Department of Internal Medicine and University of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan, USA;Department of Internal Medicine and University of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan, USA; | |
| 关键词: cytokines; IL-10; BMT; GVHD; Tregs; | |
| DOI : 10.1189/jlb.1011510 | |
| 学科分类:生理学 | |
| 来源: Federation of American Societies for Experimental Biology | |
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【 摘 要 】
IL-10 is a key immune-regulatory cytokine, and its gene polymorphisms correlate with severity of clinical GVHD. IL-10 is made by a variety of donor and host cells, but the functional relevance of its source and its role in the biology of acute GVHD are not well understood. We used preclinical models to examine the relevance of IL-10−/− in donor and host cellular subsets on the severity of GVHD. IL-10−/− in host tissues or in the donor grafts did not alter donor Teff-mediated severity of GVHD. Furthermore, neither host-derived nor donor Teff-derived IL-10 was required for regulation of GVHD by WT CD4+CD25+ donor Tregs. By contrast, Treg-derived IL-10, although not obligatory, was necessary for optimal reduction of GVHD by mature donor Tregs. Importantly, IL-10 from donor BM grafts was also critical for optimal donor Treg-mediated suppression of GVHD. Together, these data suggest that IL-10 does not contribute to the induction of GVHD severity by the Teffs. However, donor BM graft and Treg-derived IL-10 are important for donor Treg-mediated suppression of GVHD.
【 授权许可】
Unknown
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO201912010183153ZK.pdf | 42KB |
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