CD161 receptor participates in both impairing NK cell cytotoxicity and the response to glycans and vimentin in patients with rheumatoid arthritis

被引:15
作者
Richter, J.
Benson, V.
Grobarova, V.
Svoboda, J.
Vencovsky, J. [2 ]
Svobodova, R. [2 ]
Fiserova, A. [1 ]
机构
[1] AS CR, Lab Nat Cell Immun, Dept Immunol & Gnotobiol, Inst Microbiol,VVI, Prague 14220 4, Czech Republic
[2] Inst Rheumatol, Prague 12850 2, Czech Republic
关键词
CD161; Rheumatoid arthritis; NK cells; MCV; PAD4; Glycosylation; MGAT5; NATURAL-KILLER-CELLS; IMMUNOGLOBULIN-G; SYNOVIAL-FLUID; HUMAN NKR-P1A; ALPHA; DIFFERENTIATION; GLYCOSYLATION; AUTOIMMUNITY; POLYMYOSITIS; ACTIVATION;
D O I
10.1016/j.clim.2010.03.005
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
We investigated the role of natural killer (NK) cells and CD161, their primary C-type-lectin-like receptor in rheumatoid arthritis (RA). Samples were compared with healthy donors (HD), dermatomyositic (DM), polymyositic (PM), and osteoarthritic (OA) patients. RA, PM, and DM NK cell cytotoxicities significantly decreased relative to the HD and OA NK cells (p<0.0001). These results correlated with an increased expression of NK cell inhibitory receptor CD161, in active disease RA patients. We demonstrated that NK cells are able to respond to mutated citrullinated vimentin (MCV), an RA-specific autoantigen, leading to increases in both PAD4 enzyme and CD161 mRNA expression. MGAT5 glycosidase involvement was detected in GlcNAc metabolism within the synoviocytes of RA patients. Our findings reveal a functional relationship between CD161 expression and NK cell cytotoxicity as well as reactivity to glycans and MCV, thus providing new insight into the pathogenesis of RA and confirming the involvement of surface glycosylation. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:139 / 147
页数:9
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