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胶原诱导性关节炎作为类风湿关节炎的模型。

Collagen-induced arthritis as a model for rheumatoid arthritis.

作者信息

Williams Richard O

机构信息

Kennedy Institute of Rheumatology Division, Imperial College London, London, UK.

出版信息

Methods Mol Med. 2004;98:207-16. doi: 10.1385/1-59259-771-8:207.

Abstract

Collagen-induced arthritis (CIA) is an animal model of rheumatoid arthritis (RA) that is widely used to address questions of disease pathogenesis and to validate therapeutic targets. Arthritis is normally induced in mice or rats by immunization with autologous or heterologous type II collagen in adjuvant. Susceptibility to collagen-induced arthritis is strongly associated with major histocompatibility complex class II genes, and the development of arthritis is accompanied by a robust T- and B-cell response to type II collagen. The chief pathological features of CIA include a proliferative synovitis with infiltration of polymorphonuclear and mononuclear cells, pannus formation, cartilage degradation, erosion of bone, and fibrosis. As in RA, pro-inflammatory cytokines, such as tumor necrosis factor alpha(TNFalpha) and interleukin (IL)-1beta, are abundantly expressed in the arthritic joints of mice with CIA, and blockade of these molecules results in a reduction of disease severity.

摘要

胶原诱导性关节炎(CIA)是类风湿性关节炎(RA)的一种动物模型,被广泛用于解决疾病发病机制问题并验证治疗靶点。通常通过在佐剂中用自体或异体II型胶原免疫来诱导小鼠或大鼠患关节炎。对胶原诱导性关节炎的易感性与主要组织相容性复合体II类基因密切相关,并且关节炎的发展伴随着对II型胶原的强烈T细胞和B细胞反应。CIA的主要病理特征包括伴有多形核细胞和单核细胞浸润的增殖性滑膜炎、血管翳形成、软骨降解、骨质侵蚀和纤维化。与RA一样,促炎细胞因子,如肿瘤坏死因子α(TNFα)和白细胞介素(IL)-1β,在患有CIA的小鼠的关节中大量表达,阻断这些分子会导致疾病严重程度降低。

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