剧目
T细胞受体
免疫学
强直性脊柱炎
人类白细胞抗原
生物
抗原
自身免疫性疾病
发病机制
T细胞
医学
免疫系统
抗体
物理
声学
作者
Jin‐Huan Cui,Yabin Jin,Kairong Lin,Ping Xiao,Xiangping Chen,Ying-ming Pan,Wei Lin,Zu-chang Wu,Dong-mei Guo,Xiaofan Mao,Chu-ling Zhang,Wen-lue Lian,Wei Luo
标识
DOI:10.1016/j.humimm.2018.03.007
摘要
Ankylosing spondylitis (AS) is a chronic and progressive autoimmune disease affecting the invasion of the spine, sacroiliac joints and peripheral joints. T cells play a vital role in the underlying pathogenesis of AS, which mediated autoimmune and inflammatory responses via specific recognition of autoantigen peptides presented by susceptibility HLA. Antigen-specific T cells triggered by HLA/antigen complexes will undergo a massive expansion that forming an uneven T cell repertoire. To enhance our understanding of T-cell-mediated autoimmune in AS, we applied TCR β chains high-throughput sequencing to AS patients for in-depth TCR repertoire analysis. A significantly lower TCR repertoire diversity was observed in peripheral blood of AS patients relative to controls. And severe patients in our AS cohort have a more restricted TCR repertoire than mild patients, suggesting that the TCR repertoire diversity might be associated with the clinical severity of disease. No V, J and VJ pairs with significant biased usage were identified, which indicated that the usage frequency deviation of certain V/J/V-J genes in AS patients is little. This is a pilot study with potentially interesting observation on reduced diversity of T cells repertoire in peripheral blood of AS patients and further studies are needed.
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