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T-cell mediated inflammatory pathway in osteoarthritis.

机译:骨关节炎中T细胞介导的炎症途径。

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Osteoarthritis (OA) is not caused by a simple consequence of aging and cartilage degradation. Based on the conventional paradigm, OA has been considered a degenerative joint disorder. However, the dominant clinical symptom has been characterized by a non-infectious chronic inflammatory condition with infiltration of inflammatory cells in the synovial tissue or synovial fluid, especially in the early stage of the disease. The inflammatory process appeared to develop degeneration of chondrocytes and/or formation of osteophytes. Immunohistochemical staining of synovial tissue with OA in the early stage, suggests the presence of T-cell infiltration in the perivascular area, some of which were CD4 positive T cells. Among the T cells, we identified the clonality of restricted TCR usage of Vbeta chain by single strand conformation polymorphism (SSCP) method on T-cell repertoire. Therefore we address the immune response in primary OA. Copyright 1999 OsteoArthritis Research Society International.
机译:骨关节炎(OA)不是由衰老和软骨退化的简单后果引起的。基于常规范例,OA被认为是退化性关节疾病。但是,主要的临床症状的特征是非感染性慢性炎症,滑膜组织或滑液中有炎性细胞浸润,特别是在疾病的早期。炎症过程似乎发展成软骨细胞变性和/或骨赘形成。早期用OA对滑膜组织进行免疫组织化学染色,表明血管周围区域存在T细胞浸润,其中一些是CD4阳性T细胞。在T细胞中,我们通过T细胞库中的单链构象多态性(SSCP)方法确定了Vbeta链限制TCR使用的克隆性。因此,我们解决了原发性OA中的免疫反应。版权所有1999国际骨关节炎研究协会。

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