Pathogenesis of ankylosing spondylitis - recent advances and future directions

被引:239
|
作者
Ranganathan, Vidya [1 ]
Gracey, Eric [1 ,2 ]
Brown, Matthew A. [3 ]
Inman, Robert D. [1 ,2 ,4 ,5 ]
Haroon, Nigil [1 ,4 ,5 ]
机构
[1] Univ Hlth Network, Krembil Res Inst, 1-60 Leonard Ave, Toronto, ON M5T 2S8, Canada
[2] Univ Toronto, Dept Immunol, 1 Kings Coll Circle, Toronto, ON M5S 1A8, Canada
[3] Queensland Univ Technol, Translat Res Inst, Inst Hlth & Biomed Innovat, Brisbane, Qld 4001, Australia
[4] Univ Toronto, Dept Med, Div Rheumatol, 399 Bathurst St, Toronto, ON M5T 2S8, Canada
[5] Toronto Western Hosp, 399 Bathurst St, Toronto, ON M5T 2S8, Canada
关键词
UNFOLDED PROTEIN RESPONSE; GENOME-WIDE ASSOCIATION; PROOF-OF-CONCEPT; T-CELLS; TH17; CELLS; FUNCTIONAL INTERACTION; INFLAMMATORY DISEASE; PERIPHERAL-BLOOD; TRIMS PRECURSORS; T(H)17 CELLS;
D O I
10.1038/nrrheum.2017.56
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Over the past 5 years, advances in high-throughput techniques and studies involving large cohorts of patients have led to considerable advances in the identification of novel genetic associations and immune pathways involved in ankylosing spondylitis (AS). These discoveries include genes encoding cytokine receptors, transcription factors, signalling molecules and transport proteins. Although progress has been made in understanding the functions and potential pathogenic roles of some of these molecules, much work remains to be done to comprehend their complex interactions and therapeutic potential in AS. In this Review, we outline the current knowledge of AS pathogenesis, including genetic risk associations, HLA-B27-mediated pathology, perturbations in antigen-presentation pathways and the contribution of the type 3 immune response.
引用
收藏
页码:359 / 367
页数:9
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