Increased IL-17 production by peripheral T helper cells after tumour necrosis factor blockade in rheumatoid arthritis is accompanied by inhibition of migration-associated chemokine receptor expression

被引:79
作者
Aerts, Nicolaas E. [1 ]
De Knop, Kathleen J. [1 ,2 ]
Leysen, Julie [1 ]
Ebo, Didier G. [1 ,2 ]
Bridts, Chris H. [1 ]
Weyler, Joost J. [3 ]
Stevens, Wim J. [1 ,2 ]
De Clerck, Luc S. [1 ,2 ]
机构
[1] Univ Antwerp, Dept Immunol Allergol Rheumatol, Fac Med, B-2610 Antwerp, Belgium
[2] Univ Antwerp Hosp, Dept Immunol Allergol Rheumatol, Edegem, Belgium
[3] Univ Antwerp, Dept Epidemiol & Community Med, B-2610 Antwerp, Belgium
基金
比利时弗兰德研究基金会;
关键词
Rheumatoid arthritis; T-lymphocytes; Tumour necrosis factor; Interleukin-17; Chemokine receptors; Adalimumab; COLLAGEN-INDUCED ARTHRITIS; HUMAN TH17 CELLS; ATOPIC-DERMATITIS; TNF-ALPHA; INTERFERON-GAMMA; DISEASE-ACTIVITY; INTERLEUKIN-17; CYTOKINE; DISTINCT; BLOOD;
D O I
10.1093/rheumatology/keq224
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Methods. Intracellular IL-17, IFN-gamma and IL-4 production and CC-chemokine receptor CCR4 and CCR6 expression were analysed flow cytometrically in peripheral memory Th cells from healthy individuals, AD and RA patients. The latter were grouped by disease activity and presence or absence of adalimumab therapy. In RA patients initiating anti-TNF therapy, cytokine production by in vitro-stimulated peripheral mononuclear cells was measured by cytometric bead array. Results. The peripheral Th17 cell frequency is elevated in AD but not in RA. In RA, Th17 cells and IL-17 production increase after anti-TNF therapy, irrespective of disease activity. Th1 cells and IFN-gamma production are elevated in remission and under anti-TNF therapy. CCR6 expression is up-regulated in Th17 cells, but RA patients in remission under anti-TNF therapy have significantly lower expression than those with active disease. Conclusions. The increase in peripheral Th17 cells in RA patients after anti-TNF therapy is accompanied by a decrease in Th17-specific CCR6 expression, which might prevent homing of these potentially pro-inflammatory cells to the synovium.
引用
收藏
页码:2264 / 2272
页数:9
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