MDSC in autoimmunity

被引:162
作者
Cripps, James G. [1 ]
Gorham, James D. [1 ,2 ]
机构
[1] Dartmouth Med Sch, Dept Microbiol & Immunol, Lebanon, NH 03756 USA
[2] Dartmouth Med Sch, Dept Pathol, Lebanon, NH 03756 USA
关键词
MDSC; Autoimmunity; Autoimmune hepatitis; EAE; IBD; Nitric oxide; CENTRAL-NERVOUS-SYSTEM; SUPPRESSOR-CELLS; T-CELLS; LIVER-DISEASE; HEPATOCELLULAR-CARCINOMA; ENCEPHALOMYELITIS EAE; MULTIPLE-SCLEROSIS; IMMUNE-RESPONSES; BONE-MARROW; IFN-GAMMA;
D O I
10.1016/j.intimp.2011.01.026
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Myeloid derived suppressor cells (MDSC) were first described nearly two decades ago. Until recently, however, descriptions of MDSC populations were found almost exclusively in animal models of cancer or in cancer patients. Over the last few years, an increasing number of reports have been published describing populations of myeloid cells with MDSC-like properties in murine models of autoimmune disease. In contrast to the proposed deleterious role of MDSC in cancer - where these cells likely inhibit tumor immunity - in the context of autoimmunity, MDSC have the potential to suppress the autoimmune response, thereby limiting tissue injury. A logical corollary of this hypothesis is that a failure of endogenous MDSC to appropriately control autoimmune T cell responses in vivo may actually contribute to the pathogenesis of autoimmune disease. (c) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:789 / 793
页数:5
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