Ulivieri Cristina, Baldari Cosima T
Department of Life Sciences, University of Siena, Via Aldo Moro, 53100 Siena, Italy.
Pharmacol Res. 2014 Oct;88:41-52. doi: 10.1016/j.phrs.2014.03.001. Epub 2014 Mar 21.
Statins, a class of drugs that act as inhibitors of cholesterol biosynthesis and protein isoprenylation, have been proposed as immunomodulatory agents due to their potent effects both on T lymphocytes and on antigen presenting cells. Unfortunately to date the benefits of statin therapy have not been unequivocally established due to contrasting results obtained in the setting of several autoimmune diseases. A major hurdle is our limited mechanistic understanding of the pleiotropic mechanisms underlying statin-mediated immunomodulation. Accumulating evidence has highlighted two CD4(+) T cell subsets, the Th17 and Treg cells, as important disease-related targets of statins. Here we shall review recent findings on the activity of statins on Th17 and Treg differentiation and effector function. Statin-based therapies of multiple sclerosis, a Th17 cell-mediated autoimmune disease, and of Systemic Lupus Erithematosus, characterized by a Th17/Treg imbalance, will be also discussed, based on animal models and clinical trials.
他汀类药物是一类可作为胆固醇生物合成和蛋白质异戊二烯化抑制剂的药物,由于其对T淋巴细胞和抗原呈递细胞均有显著作用,已被提议作为免疫调节剂。遗憾的是,由于在几种自身免疫性疾病中获得的结果相互矛盾,他汀类药物治疗的益处至今尚未明确确立。一个主要障碍是我们对他汀类药物介导的免疫调节所涉及的多效性机制的理解有限。越来越多的证据表明,两个CD4(+) T细胞亚群,即Th17细胞和调节性T细胞(Treg),是他汀类药物重要的疾病相关靶点。在此,我们将综述他汀类药物对Th17和Treg细胞分化及效应功能影响的最新研究结果。还将基于动物模型和临床试验,讨论以Th17细胞介导的自身免疫性疾病——多发性硬化症以及以Th17/Treg失衡为特征的系统性红斑狼疮的他汀类药物治疗。