系统性红斑狼疮的研究进展

Güllü Sandal Uzun, Rym Abida, David A Isenberg
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引用次数: 0

摘要

系统性红斑狼疮(SLE)是一种慢性自身免疫性疾病,具有异质性病程和系统性累及。这是一个复杂的致病途径的结果,最终在自身抗体的形成。环境因素和遗传易感性之间的相互作用是这一过程的关键。全基因组关联研究已经确认了200个与SLE相关的基因座,这些基因座导致关键蛋白的形成,每个基因座都小幅增加了患病风险。疾病管理方面的进展包括新的经过验证的标准化工具,用于临床和研究目的,以捕捉疾病活动、损害和生活质量。在过去的50年中,由于更好的一般管理和特异性治疗,包括更好地使用免疫抑制剂,SLE的预后有了很大的改善。包括嵌合抗原受体T细胞疗法在内的生物疗法的发展为进一步改善提供了现实的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advances in systemic lupus erythematosus
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with a heterogeneous course and systemic involvement. It is the result of a complex pathogenic pathway that culminates in autoantibody formation. The interaction between environmental triggers and genetic susceptibility is key in this process. Genome-wide association studies have recognized >200 loci associated with SLE that lead to the formation of key proteins, each contributing a small increase to the risk. Advances in the management of the disease include new validated standardized tools to capture disease activity, damage and quality of life, for clinical and research purposes. The prognosis of SLE has greatly improved in the last 50 years because of better general management and specific treatment, including a better use of immunosuppressive agents. The development of biological therapies including chimeric antigen receptor T cell therapy offers the realistic prospect of further improvement.
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