Division of Rheumatology/Allergy and Clinical Immunology, School of Medicine, University of California, Davis, CA 95616, USA.
Autoimmun Rev. 2010 Mar;9(5):A400-5. doi: 10.1016/j.autrev.2009.12.009. Epub 2009 Dec 24.
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.
免疫学、分子生物学和生物信息学的最新进展为自身免疫的病理生理机制提供了广泛的信息,这极大地促进了自身免疫性疾病治疗中潜在治疗靶点的识别和基因治疗的发展。临床前研究在动物模型中进行。这种现象在两种典型的自身免疫性疾病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)模型和类风湿关节炎(RA)的胶原诱导关节炎(CIA)模型。在这里,我们讨论了这两种模型中基因治疗在自身免疫中的发展和验证的最新数据。临床前动物模型研究的成功为基因治疗在自身免疫性疾病治疗中的潜在未来应用提供了概念验证。此外,从流行病学研究中确定的风险因素揭示了在动物模型中进一步检查的潜在治疗靶点。