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小鼠胶原诱导性关节炎的免疫遗传学:人类多关节炎的一个模型

Immunogenetics of collagen induced arthritis in mice: a model for human polyarthritis.

作者信息

Moder K G, Nabozny G H, Luthra H S, David C S

机构信息

Department of Immunology, Mayo Clinic, Rochester, MN 55905.

出版信息

Reg Immunol. 1992 Sep-Oct;4(5):305-13.

PMID:1283954
Abstract

Collagen induced arthritis is an experimental animal model of inflammatory polyarthropathy that has many features of human rheumatoid arthritis. Type II collagen is the major matrix protein of hyaline cartilage and is a sequestered protein which can be presented as an autoantigen under certain conditions. To induce CIA, type II collagen is injected intradermally with complete Freund's adjuvant. Susceptibility to CIA is dependent on the presence of the trimolecular complex: 1) the arthritogenic epitope on the type II collagen; 2) a class II MHC molecule on the accessory cell presenting the arthritogenic epitope; and 3) T cells expressing specific V beta chains in their TCRs. Complement and other non-MHC background genes also may play a role in susceptibility to CIA. Both cell mediated and humoral immunity are involved in the pathogenesis of CIA. To date immunotherapies that have modulated CIA include use of anti-class Ii antibodies, anti-lymphokines, and monoclonal antibodies directed against specific cellular markers. All of these therapies are able to modulate disease to some extent but lack the specificity and efficacy to make them practical for widespread use in human disease. Most promising, is the use of monoclonal antibodies directed against specific V beta TCR subsets. This is potentially a very specific and effective therapy because it will affect only the cells involved in disease while leaving the host otherwise immunocompetent. Therapies on the horizon include the use of synthetic peptides with sequences homologous to various regions on the TCR, immunotoxins, and superantigens to modulate the immune response and ameliorate disease.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

胶原诱导性关节炎是一种炎症性多关节炎的实验动物模型,具有许多人类类风湿关节炎的特征。II型胶原是透明软骨的主要基质蛋白,是一种隐蔽蛋白,在某些条件下可作为自身抗原呈递。为诱导胶原诱导性关节炎,将II型胶原与完全弗氏佐剂皮内注射。对胶原诱导性关节炎的易感性取决于三分子复合物的存在:1)II型胶原上的致关节炎表位;2)呈递致关节炎表位的辅助细胞上的II类主要组织相容性复合体分子;3)在其T细胞受体中表达特定Vβ链的T细胞。补体和其他非主要组织相容性复合体背景基因也可能在对胶原诱导性关节炎的易感性中起作用。细胞介导免疫和体液免疫均参与胶原诱导性关节炎的发病机制。迄今为止,已调节胶原诱导性关节炎的免疫疗法包括使用抗II类抗体、抗淋巴因子和针对特定细胞标志物的单克隆抗体。所有这些疗法都能在一定程度上调节疾病,但缺乏特异性和有效性,使其无法广泛应用于人类疾病。最有前景的是使用针对特定VβT细胞受体亚群的单克隆抗体。这可能是一种非常特异且有效的疗法,因为它只会影响参与疾病的细胞,而使宿主在其他方面保持免疫活性。即将出现的疗法包括使用与T细胞受体上不同区域序列同源的合成肽、免疫毒素和超抗原来调节免疫反应并改善疾病。(摘要截短于250字)

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