Defects of mitogen-activated protein kinase in ICOS signaling pathway lead to CD4+ and CD8+ T-cell dysfunction in patients with active SLE

被引:8
作者
Cai Gang [1 ]
Yang Jiahui [1 ]
Wang Huaizhou [1 ]
Cai Qing [2 ]
Zhao Dongbao [2 ]
Shen Qian [1 ]
机构
[1] Shanghai Changhai Hosp, Dept Expt Diag, Shanghai 200433, Peoples R China
[2] Shanghai Changhai Hosp, Dept Rheumatol, Shanghai, Peoples R China
关键词
Systemic lupus erythematosus; MAP kinase; IL-2; Inducible costimulator; SYSTEMIC-LUPUS-ERYTHEMATOSUS; INDUCIBLE COSTIMULATOR; B-CELL; EXPRESSION; MOLECULE; CD28; PROLIFERATION; INVOLVEMENT; AILIM/ICOS; CRITERIA;
D O I
10.1016/j.cellimm.2009.03.016
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
in this study, hypoproliferation and defects of effectors and cytokines in CD4(+) and CD8(+) T-cells via ICOS costimulation were found in active SLE patients, relative to normal individuals and RA patient controls. Exogenous IL-2 can partially reverse those defects. In addition, low level of ERK phosphorylation in ICOS-mediated signaling pathway was discovered in lupus CD4(+) and CD8(+) T-cells. When blocked with ERK-specific chemical inhibitor PD98059, cell proliferation and IL-2 production via ICOS costimulation from both CD4(+) and CD8(+) T-cells will be severely inhibited. These findings confirmed the dysfunction of both CD4(+) and CD8(+) T-cells after ICOS costimulation in lupus patients and most importantly pointed out that impairment of ERK activation might be one of the critical factors involved in ICOS-mediated IL-2 and T-cell hypoproliferation in active SLE. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:83 / 89
页数:7
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