Innate mucosal-associated invariant T (MAIT) cells are activated in inflammatory bowel diseases

被引:291
作者
Serriari, N-E [1 ]
Eoche, M. [2 ]
Lamotte, L. [6 ]
Lion, J. [1 ]
Fumery, M. [2 ]
Marcelo, P. [3 ]
Chatelain, D. [4 ]
Barre, A. [1 ,5 ]
Nguyen-Khac, E. [2 ]
Lantz, O. [7 ]
Dupas, J-L [2 ]
Treiner, E. [1 ,5 ]
机构
[1] Avenir Inserm UMR925 Grp, Amiens, France
[2] CHU Amiens, Hepatogastroenterol Dept, Amiens, France
[3] UPJV, ICAP Facil, Amiens, France
[4] CHU Amiens, Dept Pathol, Amiens, France
[5] CHU Amiens, Dept Immunol, Amiens, France
[6] UPJV, EA 4666, Amiens, France
[7] Inst Curie, Inserm UMR932, Paris, France
关键词
inflammatory bowel diseases; innate T cells; MHC class I-like; immune system; NATURAL-KILLER-CELLS; IMPROVES CYTOTOXICITY; ULCERATIVE-COLITIS; EXPRESSION; CYTOKINES; DEFINES; NKG2D; BLOOD; IL-13;
D O I
10.1111/cei.12277
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
Inflammatory bowel diseases are characterized by a deregulated immune response targeting the gut bacterial flora. Mucosal-associated invariant T (MAIT) cells are major histocompatibility complex (MHC) class Ib-restricted innate-like lymphocytes with anti-bacterial functions. They display an effector/memory phenotype and are found in large numbers in the blood, mucosae and liver. They have also been implicated in inflammatory diseases such as multiple sclerosis. Therefore, we aimed to analyse the possible involvement of MAIT cells in Crohn's disease (CD) and ulcerative colitis (UC). To this end, a phenotypical and functional analysis of MAIT cells isolated from the blood of healthy subjects, CD and UC patients was undertaken. MAIT cells were also quantified in ileal biopsies of CD patients. The frequency of blood MAIT cells was specifically reduced in IBD patients compared with healthy donors, whereas it was dramatically greater in the inflamed versus healthy tissue. MAIT cells were activated as they expressed significantly more the Ki67 antigen, and this was accompanied by phenotypical changes such as increased expression of natural killer (NK)G2D and B and T lymphocyte attenuator (BTLA). Finally, in-vitro-activated MAIT cells from CD and UC patients secreted significantly more interleukin (IL)-17, together with a decreased interferon (IFN)-gamma in CD but an increased IL-22 in UC. These data show that MAIT cells are activated in IBD, which results in an increased recruitment towards the inflamed tissues, an altered phenotype and a switch in the pattern of cytokine secretion. This is the first demonstration that MAIT cells are immune players in IBD, whose precise functions in this context need to be addressed.
引用
收藏
页码:266 / 274
页数:9
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