Chernajovsky Y, Dreja H, Daly G, Annenkov A, Gould D, Adams G, Croxford J L, Baker D, Podhajcer O L, Mageed R A
Bone and Joint Research Unit, St. Bartholomew's and Royal London School of Medicine and Dentistry, Queen Mary and Westfield College, Charterhouse Square, London EC1M 6BQ, UK.
Genes Immun. 2000 Jun;1(5):295-307. doi: 10.1038/sj.gene.6363683.
Animal models of autoimmune disease have been developed that mimic some aspects of the pathophysiology of human disease. These models have increased our understanding of possible mechanisms of pathogenesis at the molecular and cellular level and have been important in the testing, development and validation of new immunotherapies. The susceptibility to develop disease in the majority of these models is polygenic as is the case in humans. The exceptions to this rule are gene knock outs and transgenic models of particular genes which, in particular genetic backgrounds, have also contributed to the understanding of single gene function and their possible contribution to pathogenesis. Gene therapy approaches that target immune functions are being developed with encouraging results, despite the polygenic nature of these diseases. Basically this novel immuno-genetic therapy harnesses the knowledge of immunology with the myriad of biotechnological breakthroughs in vector design and delivery. Autoimmune disease is the result of genetic dysregulation which could be controlled by gene therapy. Here we summarize the genetic basis of these human diseases as well as some of the best characterized murine models. We discuss the strategies for their treatment using immuno- and gene therapy.
已经开发出了自身免疫性疾病的动物模型,这些模型模拟了人类疾病病理生理学的某些方面。这些模型增进了我们在分子和细胞水平上对发病机制可能机制的理解,并且在新免疫疗法的测试、开发和验证中发挥了重要作用。在大多数这些模型中,发病易感性是多基因的,人类疾病也是如此。这条规则的例外是基因敲除和特定基因的转基因模型,在特定的遗传背景下,这些模型也有助于理解单基因功能及其对发病机制的可能贡献。尽管这些疾病具有多基因性质,但针对免疫功能的基因治疗方法正在开发中,并且取得了令人鼓舞的结果。基本上,这种新型免疫基因疗法利用了免疫学知识以及载体设计和递送方面众多的生物技术突破。自身免疫性疾病是基因失调的结果,而基因治疗可以对其进行控制。在这里,我们总结了这些人类疾病的遗传基础以及一些特征最明显的小鼠模型。我们讨论了使用免疫疗法和基因疗法治疗这些疾病的策略。