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小鼠胶原诱导性关节炎

Collagen-induced arthritis in mice.

作者信息

Williams Richard O

机构信息

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

出版信息

Methods Mol Med. 2007;136:191-9. doi: 10.1007/978-1-59745-402-5_14.

Abstract

Collagen-induced arthritis in mice has been widely used to address questions of disease pathogenesis and to validate therapeutic targets for human rheumatoid arthritis. Arthritis is normally observed about 3 wk after immunization with autologous or heterologous type II collagen in complete Freund's adjuvant and susceptibility to the disease is strongly associated with major histocompatibility complex class II genes. The development of collagen-induced arthritis is associated with strong T- and B-cell responses to type II collagen and the chief pathological features of the disease include a proliferative synovitis with infiltration of polymorphonuclear and mononuclear cells, pannus formation, cartilage degradation, erosion of bone and fibrosis. Proinflammatory cytokines, such as tumor necrosis factor-alpha and interleukin--1beta, are abundantly expressed in the arthritic joints of mice with collagen-induced arthritis and, as in human rheumatoid arthritis, blockade of these molecules is effective in reducing the severity of disease.

摘要

小鼠胶原诱导性关节炎已被广泛用于解决疾病发病机制问题,并验证人类类风湿关节炎的治疗靶点。在用完全弗氏佐剂中的自体或异体II型胶原免疫后约3周通常会观察到关节炎,且对该疾病的易感性与主要组织相容性复合体II类基因密切相关。胶原诱导性关节炎的发展与对II型胶原的强烈T细胞和B细胞反应有关,该疾病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、骨侵蚀和纤维化。促炎细胞因子,如肿瘤坏死因子-α和白细胞介素-1β,在胶原诱导性关节炎小鼠的关节中大量表达,并且与人类类风湿关节炎一样,阻断这些分子可有效减轻疾病的严重程度。

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