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贝拉西普在肾移植中的应用:回顾过去,塑造未来。

Belatacept in Kidney Transplantation: Reflecting on the Past, Shaping the Future.

作者信息

Noble Johan, Leon Juliette, Del Bello Arnaud, Anglicheau Dany, Blancho Gilles, Ville Simon, Couzi Lionel, Grimbert Philippe, Le Meur Yannick, Moulin Bruno, Kamar Nassim, Rostaing Lionel, Herr Florence, Durrbach Antoine, Bertrand Dominique

机构信息

Nephrology, Hemodialysis, Apheresis and Transplantation, Centre Hospitalier Universitaire (CHU) Grenoble-Alpes, La Tronche, France.

University Grenoble Alpes, Centre National de la Recherche Scientifique (CNRS), Institut National de la Santé et de la Recherche Médicale (INSERM), Centre Hospitalier Universitaire (CHU) Grenoble Alpes, Institute for Advanced Biosciences (IAB), Grenoble, France.

出版信息

Transpl Int. 2025 May 20;38:14412. doi: 10.3389/ti.2025.14412. eCollection 2025.

Abstract

Calcineurin inhibitors (CNIs) are a cornerstone of post-transplant immunosuppressive regimens. However, their use is associated with adverse effects, most notably chronic nephrotoxicity, which remains a leading cause of long-term allograft dysfunction. Belatacept, a selective costimulation blocker, offers a promising alternative to CNIs by aiming to reduce nephrotoxicity while maintaining efficacy in preventing acute rejection. While its use in transplantation has been associated with improved graft and patient survival, it has also been linked to a higher incidence of acute rejection. Early post-transplantation conversion to belatacept has demonstrated significant improvements in renal function (eGFR gains ranging from +8.8 to +38.2 mL/min/1.73 m at 1 year post-conversion) but carries a higher risk of opportunistic infections. Late conversion protocols, typically initiated beyond 6 months post-transplantation, have shown sustained-although less pronounced-eGFR improvements and better long-term graft survival compared to CNI-based regimens. Additionally, belatacept appears to reduce the incidence of donor-specific antibodies. Future directions for the use of belatacept need further exploration, including its role in rescuing poor renal function, its combination with low-dose CNIs, mTOR inhibitors, or tocilizumab, and its application in desensitization protocols. By potentially striking a balance between efficacy and safety, belatacept may redefine the future landscape of transplant immunosuppression.

摘要

钙调神经磷酸酶抑制剂(CNIs)是移植后免疫抑制方案的基石。然而,其使用会带来不良反应,最显著的是慢性肾毒性,这仍然是长期移植器官功能障碍的主要原因。贝拉西普是一种选择性共刺激阻滞剂,旨在降低肾毒性,同时保持预防急性排斥反应的疗效,为CNIs提供了一种有前景的替代方案。虽然其在移植中的使用与移植器官和患者存活率的提高有关,但也与急性排斥反应的发生率较高有关。移植后早期转换为贝拉西普已证明肾功能有显著改善(转换后1年时估算肾小球滤过率(eGFR)增加范围为+8.8至+38.2 mL/min/1.73 m²),但机会性感染风险较高。晚期转换方案通常在移植后6个月后开始,与基于CNIs的方案相比,已显示出持续的(尽管不太明显)eGFR改善和更好的长期移植器官存活。此外,贝拉西普似乎能降低供体特异性抗体的发生率。贝拉西普使用的未来方向需要进一步探索,包括其在挽救肾功能不佳方面的作用、与低剂量CNIs、雷帕霉素靶蛋白(mTOR)抑制剂或托珠单抗的联合使用,以及其在脱敏方案中的应用。通过在疗效和安全性之间可能取得平衡,贝拉西普可能会重新定义移植免疫抑制的未来格局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14f1/12129774/3ca35c951933/ti-38-14412-g001.jpg

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