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Development and validation of gene therapies in autoimmune diseases: Epidemiology to animal models.

机译:自身免疫性疾病基因疗法的开发和验证:动物模型的流行病学。

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摘要

Recent advancement in immunology, molecular biology, and bioinformatics has yielded extensive information on the pathophysiological mechanisms of autoimmunity, which has greatly facilitated the identification of potential therapeutic targets and the development of gene therapy in the treatment of autoimmune disease. Preclinical studies were carried out in animal models. This phenomenon is well illustrated in two prototypic animal models of autoimmune disease: the autoimmune encephalomyelitis (EAE) model of multiple sclerosis (MS) and collagen-induced arthritis (CIA) model in rheumatoid arthritis (RA). Here we discuss the current data on the development and validation of gene therapy in autoimmunity in these two models. The success in preclinical animal model studies provides the proof-of-concept of gene therapy for potential future applications in the treatment of autoimmune diseases. Furthermore, the identification of risk factors from epidemiological studies reveals further potential therapeutic targets to be examined in animal models.
机译:免疫学,分子生物学和生物信息学的最新进展已经获得了有关自身免疫的病理生理机制的广泛信息,这极大地促进了潜在免疫靶点的鉴定和基因疗法在自身免疫性疾病治疗中的发展。在动物模型中进行了临床前研究。这种现象在两种自身免疫性疾病的原型动物模型中得到了很好的说明:多发性硬化症(MS)的自身免疫性脑脊髓炎(EAE)模型和类风湿性关节炎(RA)的胶原蛋白诱导的关节炎(CIA)模型。在这里,我们讨论了这两种模型中有关自身免疫性基因治疗的发展和验证的当前数据。临床前动物模型研究的成功提供了基因疗法的概念证明,可用于未来在自身免疫性疾病治疗中的应用。此外,通过流行病学研究确定的危险因素揭示了在动物模型中需要检查的其他潜在治疗目标。

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