T cells as a therapeutic target in SLE

被引:85
作者
Comte, D. [1 ,2 ]
Karampetsou, M. P. [1 ]
Tsokos, G. C. [1 ]
机构
[1] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Div Rheumatol, Boston, MA 02215 USA
[2] CHU Vaudois, Div Immunol & Allergy, Lausanne, Switzerland
基金
美国国家卫生研究院;
关键词
Systemic lupus erythematosus; T cells; interleukin-2 (IL-2); epigenetics; treatment; SYSTEMIC-LUPUS-ERYTHEMATOSUS; ANTI-INTERLEUKIN-17A MONOCLONAL-ANTIBODY; SUPPRESSES IL-2 PRODUCTION; SPLEEN TYROSINE KINASE; RECEPTOR ZETA-CHAIN; ELEMENT MODULATOR; DOUBLE-BLIND; RENAL-DISEASE; T(H)17 CELLS; CD40; LIGAND;
D O I
10.1177/0961203314556139
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease characterized by a loss of tolerance to multiple endogenous antigens. SLE etiology remains largely unknown, despite recent insight into the immunopathogenesis of the disease. T cells are important in the development of the disease by amplifying the immune response and contributing to organ damage. Aberrant signaling, cytokine secretion, and tissue homing displayed by SLE T cells have been extensively studied and the underlying pathogenic molecular mechanisms are starting to be elucidated. T-cell-targeted treatments are being explored in SLE patients. This review is an update on the T-cell abnormalities and related therapeutic options in SLE.
引用
收藏
页码:351 / 363
页数:13
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