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主要组织相容性复合体基因在小鼠胶原诱导性关节炎中的作用:人类类风湿性关节炎的一个模型

Role of major histocompatibility complex genes in murine collagen-induced arthritis: a model for human rheumatoid arthritis.

作者信息

David Chella S, Taneja Veena

机构信息

Department of Immunology, Mayo Clinic-Rochester, Rochester, Minnesota 55905, USA.

出版信息

Am J Med Sci. 2004 Apr;327(4):180-7. doi: 10.1097/00000441-200404000-00003.

Abstract

Collagen-induced arthritis is an animal model for rheumatoid arthritis that shares a number of clinical, hematologic, serologic, and radiographic features with human disease. Predisposition to rheumatoid arthritis has been associated with major histocompatibility complex (MHC) class II genes, HLA-DRB0401/DQB10302 and resistance to DRB1*0402 and DQ6 genes. Animal models allow one to study the genetics and immunologic processes of individual genes involved in the complex human diseases. To study the interactions between class II molecules and to define their role in arthritis, the authors generated HLA-DR and -DQ transgenic mice. HLA transgenes are expressed on cell surface and can positively select CD4 cells. A peripheral tolerance is maintained to the trans-genes even though an efficient T cell response to immunodominant antigens similar to human T cells is observed. Using HLA-DQ/DR double transgenic mice, the studies show that complementation between DQ and DR molecules contributes to predisposition to and severity of, or protection from, arthritis. Thus, these mice provide a powerful tool to understand the role of HLA molecules in the predisposition to and immunotherapy for human disease.

摘要

胶原诱导性关节炎是类风湿关节炎的一种动物模型,它与人类疾病具有许多临床、血液学、血清学和影像学特征。类风湿关节炎的易感性与主要组织相容性复合体(MHC)II类基因、HLA - DRB0401/DQB10302相关,而对DRB1*0402和DQ6基因具有抗性。动物模型使人们能够研究参与复杂人类疾病的单个基因的遗传学和免疫过程。为了研究II类分子之间的相互作用并确定它们在关节炎中的作用,作者培育了HLA - DR和 - DQ转基因小鼠。HLA转基因在细胞表面表达,并能阳性选择CD4细胞。尽管观察到对与人T细胞相似的免疫显性抗原具有有效的T细胞反应,但对转基因仍维持外周耐受性。使用HLA - DQ/DR双转基因小鼠的研究表明,DQ和DR分子之间的互补作用有助于关节炎的易感性、严重程度或对其的保护作用。因此,这些小鼠为理解HLA分子在人类疾病易感性和免疫治疗中的作用提供了一个有力的工具。

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