Geissler Ina, Collins Louise, Schofield Rebecca, Fabre John W
Department of Clinical Sciences, Guy's, King's & St. Thomas' School of Medicine, The Rayne Institute, King's Denmark Hill Campus, 123 Coldharbour Lane, London SE5 9NU, United Kingdom.
Transplantation. 2006 Mar 27;81(6):922-6. doi: 10.1097/01.tp.0000179154.17329.68.
Vascular endothelial cells of man and pig, but not rodents, strongly express major histocompatibility complex (MHC) class II antigens in vivo, probably via the inducible promoter IV of the class II transactivator. There is abundant in vitro evidence that MHC class II positive vascular endothelial cells can activate T cells. Peripheral antigen presentation by endothelial cells is potentially important for organ-specific immunity, for allograft rejection, and possibly for immune responsiveness in general. Given the reported effects of statins on promoter IV of the class II transactivator, we evaluated in vivo expression of MHC class II antigens in pigs treated with atorvastatin calcium.
Pigs were given 3 mg/kg/day of atorvastatin orally daily for 16 days, and then killed 24 hr after the last dose. Heart, kidney, and liver were removed for immunohistological and quantitative absorption analysis.
Double-labeling studies using immunofluorescence on frozen section for Factor VIII and MHC class II showed a marked suppression of MHC class II on vascular endothelial cells in all 4 treated pigs, in comparison with untreated pigs. This was confirmed using immunoperoxidase techniques on frozen sections. Quantitative absorption analysis showed up to 25-fold reduction in MHC class II expression.
Statins substantially suppress endothelial cell MHC class II expression in vivo. This is likely to inhibit organ-specific immune responses, and possibly also general immune responsiveness. In a transplantation setting, in addition to other regulatory effects on the recipients immune system, statins might reduce the long-term capacity of the donor organ to activate rejection mechanisms.
人和猪的血管内皮细胞,而非啮齿动物的血管内皮细胞,在体内强烈表达主要组织相容性复合体(MHC)II类抗原,可能是通过II类反式激活因子的诱导型启动子IV。有大量体外证据表明,MHC II类阳性血管内皮细胞可激活T细胞。内皮细胞在外周的抗原呈递对于器官特异性免疫、同种异体移植排斥反应以及可能的总体免疫反应性都具有潜在重要性。鉴于他汀类药物对II类反式激活因子启动子IV的报道作用,我们评估了阿托伐他汀钙治疗的猪体内MHC II类抗原的表达情况。
给猪每日口服3mg/kg的阿托伐他汀,持续16天,然后在最后一剂后24小时处死。取出心脏、肾脏和肝脏进行免疫组织学和定量吸收分析。
与未治疗的猪相比,对4只治疗猪的冰冻切片进行因子VIII和MHC II类的免疫荧光双标记研究显示,血管内皮细胞上的MHC II类明显受到抑制。这在冰冻切片上用免疫过氧化物酶技术得到了证实。定量吸收分析显示MHC II类表达降低了25倍。
他汀类药物在体内可显著抑制内皮细胞MHC II类的表达。这可能会抑制器官特异性免疫反应,也可能抑制总体免疫反应性。在移植环境中,除了对受体免疫系统的其他调节作用外,他汀类药物可能会降低供体器官激活排斥机制的长期能力。