Why do intestinal epithelial cells express MHC class II?

被引:37
|
作者
Heuberger, Cornelia [1 ,2 ]
Pott, Johanna [1 ,3 ]
Maloy, Kevin Joseph [1 ,4 ]
机构
[1] Univ Oxford, Sir William Dunn Sch Pathol, Oxford, England
[2] Univ Oxford, Kennedy Inst Rheumatol, Oxford, England
[3] Hubrecht Organoid Technol, Utrecht, Netherlands
[4] Univ Glasgow, Inst Infect Immun & Inflammat, 120 Univ Pl, Glasgow G12 8TA, Lanark, Scotland
基金
英国惠康基金;
关键词
CD4+T cells; gut; intestinal epithelial cell; MHC class II; HLA-DR EXPRESSION; IFN-GAMMA; ANTIGEN PRESENTATION; HUMAN CYTOMEGALOVIRUS; DENDRITIC CELLS; IA ANTIGENS; TUFT CELLS; TGF-BETA; T-CELLS; COMPLEX;
D O I
10.1111/imm.13270
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Intestinal epithelial cells (IECs) constitute the border between the vast antigen load present in the intestinal lumen and the mucosal immune compartment. Their ability to express antigen processing and presentation machinery evokes the question whether IECs function as non-conventional antigen-presenting cells. Major histocompatibility complex (MHC) class II expression by non-haematopoietic cells, such as IECs, is tightly regulated by the class II transactivator (CIITA) and is classically induced by IFN-gamma. As MHC class II expression by IECs is upregulated under inflammatory conditions, it has been proposed to activate effector CD4+ T (Teff) cells. However, other studies have reported contradictory results and instead suggested a suppressive role of antigen presentation by IECs, through regulatory T (Treg)-cell activation. Recent studies investigating the role of MHC class II + exosomes released by IECs also reported conflicting findings of either immune enhancing or immunosuppressive activities. Moreover, in addition to modulating inflammatory responses, recent findings suggest that MHC class II expression by intestinal stem cells may elicit crosstalk that promotes epithelial renewal. A more complete understanding of the different consequences of IEC MHC class II antigen presentation will guide future efforts to modulate this pathway to selectively invoke protective immunity while maintaining tolerance to beneficial antigens.
引用
收藏
页码:357 / 367
页数:11
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