Immune checkpoint receptors in regulating immune reactivity in rheumatic disease

被引:53
作者
Ceeraz, Sabrina [1 ]
Nowak, Elizabeth C. [1 ]
Burns, Christopher M. [2 ]
Noelle, Randolph J. [1 ,3 ,4 ]
机构
[1] Geisel Sch Med Dartmouth, Norris Cotton Canc Ctr, Dept Microbiol & Immunol, Lebanon, NH 03756 USA
[2] Geisel Sch Med Dartmouth, Dartmouth Hitchcock Med Ctr, Rheumatol Sect, Dept Med, Lebanon, NH 03756 USA
[3] Kings Coll London, Guys Hosp, Ctr Transplantat, MRC, London SE1 9RT, England
[4] Kings Coll London, Kings Hlth Partners, Dept Immune Regulat & Intervent, London SE1 9RT, England
基金
英国惠康基金;
关键词
SYSTEMIC-LUPUS-ERYTHEMATOSUS; PRIMARY SJOGRENS-SYNDROME; COLLAGEN-INDUCED ARTHRITIS; JUVENILE IDIOPATHIC ARTHRITIS; GLAND EPITHELIAL-CELLS; PLACEBO-CONTROLLED TRIAL; WHITE)F-1 MICE PROMOTES; CD4(+) T-CELLS; CD40; LIGAND; AUTOIMMUNE-DISEASES;
D O I
10.1186/s13075-014-0469-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Immune checkpoint regulators are critical modulators of the immune system, allowing the initiation of a productive immune response and preventing the onset of autoimmunity. Co-inhibitory and co-stimulatory immune checkpoint receptors are required for full T-cell activation and effector functions such as the production of cytokines. In autoimmune rheumatic diseases, impaired tolerance leads to the development of diseases such as rheumatoid arthritis, systemic lupus erythematosus, and Sjogren's syndrome. Targeting the pathways of the inhibitory immune checkpoint molecules CD152 (cytotoxic T lymphocyte antigen-4) and CD279 (programmed death-1) in cancer shows robust anti-tumor responses and tumor regression. This observation suggests that, in autoimmune diseases, the converse strategy of engaging these molecules may alleviate inflammation owing to the success of abatacept (CD152-Ig) in rheumatoid arthritis patients. We review the preclinical and clinical developments in targeting immune checkpoint regulators in rheumatic disease.
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页数:12
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