内质网
强直性脊柱炎
发病机制
医学
计算生物学
免疫学
生物
遗传学
作者
Tony J. Kenna,Philip Robinson,Nigil Haroon
出处
期刊:Rheumatology
[Oxford University Press]
日期:2015-09-01
卷期号:54 (9): 1549-1556
被引量:30
标识
DOI:10.1093/rheumatology/kev218
摘要
There has been significant progress in our understanding of the pathogenesis of AS. The advent of genome-wide association studies has increased the known loci associated with AS to more than 40. The endoplasmic reticulum resident aminopeptidases (ERAP) 1 and 2 were identified in this manner and are of particular interest. There appears to be a genetic as well as a functional interaction of ERAP1 and 2 with HLA-B27 based on the known functions of these molecules. Recent studies on the structure, immunological effects and the peptide-trimming properties of ERAP 1 and 2 have helped to provide insight into their pathogenic potential in AS. In this review, we explore the role of ERAP 1 and 2 in the pathogenesis of AS.
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