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自身免疫性疾病的基因治疗:挑战与机遇。

Gene therapy in autoimmune diseases: challenges and opportunities.

机构信息

Division of Rheumatology/Allergy and Clinical Immunology, School of Medicine, University of California, Davis, CA 95616, United States.

出版信息

Autoimmun Rev. 2010 Jan;9(3):170-4. doi: 10.1016/j.autrev.2009.10.004. Epub 2009 Oct 23.

Abstract

Clinical treatment of autoimmune disorders presents a special challenge. For decades, most clinical regimens in autoimmunity has been largely symptomatic and non-disease specific. Although data from vigorous research has lead to accumulating knowledge on the pathogenic and immunological mechanisms of many autoimmune diseases, their direct clinical applications have been sparse. Advances in biotechnology have laid the groundwork for potent and specific molecular targeting therapies by gene therapy, and have just begun to be investigated in the treatment of autoimmune disorders. Such work has been largely based on the availability of well-established animal models of common autoimmune disorders, and the efficacy of strategic approaches initially investigated and validated in these models. Although these preclinical animal model studies have provided the proof-of-concept for multiple potential applications, human clinical trials on gene therapy in autoimmunity are still at its infancy. The recent success of Phase I/II clinical trials of gene therapy in rheumatoid arthritis and multiple sclerosis, development of cutting edge technology in target identification, as well as gene delivery systems have now set the stage for a more thorough and vigorous pace in the near future to advance this exciting field.

摘要

自身免疫性疾病的临床治疗提出了特殊的挑战。几十年来,大多数自身免疫的临床方案主要是对症治疗且非针对疾病本身。虽然大量的研究数据已经积累了许多自身免疫性疾病的发病和免疫学机制的知识,但这些知识的临床直接应用仍然很少。生物技术的进步为基因治疗等强效和特异性的分子靶向治疗奠定了基础,并且刚刚开始在自身免疫性疾病的治疗中进行研究。这些工作主要基于常见自身免疫性疾病的成熟动物模型的可用性,以及最初在这些模型中研究和验证的策略方法的有效性。尽管这些临床前动物模型研究为多种潜在应用提供了概念验证,但自身免疫性疾病的基因治疗的人体临床试验仍处于起步阶段。最近在类风湿关节炎和多发性硬化症的基因治疗的 I/II 期临床试验取得的成功、目标识别的尖端技术的发展以及基因传递系统的发展,为在不久的将来更全面和更有力地推进这一令人兴奋的领域奠定了基础。

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