环孢素a诱导的自身免疫:人类硬皮病的动物模型

J. Damoiseaux, H. van der Heijden, J. van de Gaar, P. van Breda Vriesman
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引用次数: 0

摘要

动物模型在阐明复杂人类疾病的病理机制方面具有重要的价值。然而,需要与人类疾病进行认真的比较,以确定各自的模型与人类情况相关的程度。在这项研究中,我们比较了环孢素a诱导的大鼠自身免疫与人硬皮病,因此我们考虑了组织和免疫病理、血管异常的存在以及循环自身抗体的发生。总之,宏观和组织病理学上的相似性是考虑环孢素a诱导自身免疫作为人类硬皮病实验模型的最重要特征。此外,病变中T细胞和巨噬细胞的存在,以及CD4 T细胞室内的外周免疫偏差是另外两个常见因素,它们证明了在进一步研究T细胞在硬皮病发病机制中的作用时,使用环孢素a诱导的自身免疫动物模型是合理的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cyclosporine A-induced autoimmunity: an animal model for human scleroderma

Animal models have been shown to be very valuable in the elucidation of pathologic mechanisms in complex human diseases. However, conscientious comparison with the human disease is required to define to what extend the respective model is relevant for the human situation. In this study we have compared Cyclosporine A-induced autoimmunity in the rat with human scleroderma and hereby we have taken into account the histo- and immunopathology, the presence of vascular abnormalities, and the occurrence of circulating autoantibodies. Altogether, the macroscopical and histopathological similarities are the most important characteristics for considering Cyclosporine A-induced autoimmunity as an experimental model for human scleroderma. Furthermore, the presence of T cells and macrophages in the lesions, as well as the peripheral immune deviation within the CD4 T cell compartment are two other common factors and they justify the use of the animal model Cyclosporine A-induced autoimmunity in further studies on the role of T cells in the pathogenesis of scleroderma.

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