摘要
背景:自身免疫性疾病是由过度活跃的免疫反应引起的疾病,包括类风湿性关节炎(RA)、干燥综合征(SS)等全身性自身免疫性疾病和1型糖尿病(T1DM)等器官特异性自身免疫性疾病,重症肌无力 (MG) 和炎症性肠病 (IBD)。目前,尚无长期治愈方法;但是,有几种治疗方法可以延缓疾病的发展,包括基因治疗,基因治疗已被仔细研究,具有治疗自身免疫性疾病的巨大能力。 目的:综述强调了导致自身免疫性疾病发展的致病机制和基因,即 T1DM、2 型糖尿病 (T2DM)、RA、SS、IBD 和 MG。此外,该审查的重点是调查在经历这些疾病的各种动物模型中传递校正基因及其特定病毒载体的结果,以确定基因治疗的有效性。 方法:从 PubMed、MEDLINE、Frontier 和其他数据库中获取了大量强调基因治疗在自身免疫性疾病管理中的巨大潜力的评论和研究文章,并为撰写这篇评论文章进行了深入研究。 结果:接受基因治疗的各种动物模型在促炎细胞因子水平、淋巴细胞浸润、与自身免疫性疾病相关的表现方面均表现出调节,并保持免疫反应平衡,从而与自身免疫性疾病的进展竞争。 结论:基因疗法在各种动物研究中揭示了自身免疫性疾病管理的惊人能力,但在将其应用于人类之前,进一步的研究对于克服与之相关的局限性至关重要。
关键词: 免疫系统、自身免疫性疾病、基因治疗、类风湿性关节炎、1型糖尿病、炎症性肠病
图形摘要
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