免疫系统
类风湿性关节炎
炎症
免疫学
蛋白酵素
生物
效应器
关节炎
细胞外基质
上睑下垂
滑膜
发病机制
先天免疫系统
获得性免疫系统
成纤维细胞
自身免疫性疾病
细胞生物学
炎症体
抗体
细胞培养
酶
生物化学
遗传学
作者
Beatrix Bartók,Gary S. Firestein
标识
DOI:10.1111/j.0105-2896.2009.00859.x
摘要
Summary: Rheumatoid arthritis (RA) remains a significant unmet medical need despite significant therapeutic advances. The pathogenesis of RA is complex and includes many cell types, including T cells, B cells, and macrophages. Fibroblast‐like synoviocytes (FLS) in the synovial intimal lining also play a key role by producing cytokines that perpetuate inflammation and proteases that contribute to cartilage destruction. Rheumatoid FLS develop a unique aggressive phenotype that increases invasiveness into the extracellular matrix and further exacerbates joint damage. Recent advances in understanding the biology of FLS, including their regulation regulate innate immune responses and activation of intracellular signaling mechanisms that control their behavior, provide novel insights into disease mechanisms. New agents that target FLS could potentially complement the current therapies without major deleterious effect on adaptive immune responses.
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