Wéclawiak H, Kamar N, Ould-Mohamed A, Cardeau-Desangles I, Rostaing L
Department of Nephrology, Dialysis and Organ Transplantation, Toulouse University Hospital, Toulouse, France.
Transplant Proc. 2010 Nov;42(9 Suppl):S29-31. doi: 10.1016/j.transproceed.2010.07.003.
Kidney transplantation can be used to replace failing native kidneys; however, it requires long-term immunosuppression, and immunological tolerance for this is not yet achievable. The cornerstone of immunosuppression is based on calcineurin inhibitors, which are nephrotoxic. Therefore, new drugs are being developed that provide efficacious immunosuppression and almost no renal toxicity. The first family of drugs that have these properties are mammalian target of rapamycin inhibitors: these include sirolimus and everolimus. These two drugs, besides their immunosuppressive properties, also have beneficial effects regarding cytomegalovirus (CMV) infection, which is a very common posttransplantation complication. In phase III trials, belatacept, a costimulatory blocker, has also been shown to provide a good immunosuppressive effect and also gives a significantly better cardiovascular profile than cyclosporine-based immunosuppression. However, belatacept can potentially increase infections such as CMV. Thus, herein, we describe the rationale for combining belatacept with sirolimus for kidney transplant patients.
肾移植可用于替代功能衰竭的自体肾;然而,这需要长期免疫抑制,而目前尚无法实现对此的免疫耐受。免疫抑制的基石是基于钙调神经磷酸酶抑制剂,这类药物具有肾毒性。因此,正在研发能提供有效免疫抑制且几乎无肾毒性的新药。具有这些特性的第一类药物是雷帕霉素靶蛋白抑制剂:包括西罗莫司和依维莫司。这两种药物除了具有免疫抑制特性外,对巨细胞病毒(CMV)感染也有有益作用,CMV感染是一种非常常见的移植后并发症。在III期试验中,共刺激阻断剂贝拉西普也已显示出良好的免疫抑制效果,并且与基于环孢素的免疫抑制相比,其心血管状况明显更好。然而,贝拉西普可能会增加如CMV等感染。因此,在此我们描述了将贝拉西普与西罗莫司联合用于肾移植患者的基本原理。