Hansen Carla M, Bachmann Sebastian, Su Mingzhen, Budde Klemens, Choi Mira
Department of Nephrology and Medical Intensive Care, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt Universität Zu Berlin, Berlin, Germany.
Acta Physiol (Oxf). 2025 May;241(5):e70047. doi: 10.1111/apha.70047.
AIM: Calcineurin inhibitors (CNIs) have revolutionized transplant medicine, improving allograft survival but posing challenges like calcineurin inhibitor-induced nephrotoxicity (CNT). Acute CNT, often dose-dependent, leads to vasoconstriction and acute kidney injury, with treatment focusing on CNI exposure reduction. Chronic CNT manifests as progressive allograft function decline, with challenges in distinguishing it from nonspecific allograft nephropathy. METHODS: This narrative review provides a concise overview of the clinical management of CNT, covering acute and chronic CNT. We reviewed original articles, landmark papers, and meta-analyses on CNT mitigation strategies, including CNI-sparing approaches. RESULTS: Preventive measures include co-medications, CNI exposure monitoring, and CNI sparing strategies, such as reducing target trough levels and converting to mTOR inhibitors (mTORi) or belatacept. Despite improvements in graft function, challenges persist in demonstrating significant differences in allograft survival with CNI-sparing regimens. The paradigm shift from chronic CNT as the main cause of chronic allograft nephropathy toward rather immunologic triggered injuries and/or comorbidities as relevant contributors to allograft deterioration over time must be kept in mind. CONCLUSION: CNIs have significantly improved kidney transplant outcomes, but their associated nephrotoxicity necessitates mitigation strategies. The decision to implement such regimens is always an individual choice balancing against the risk of immunologic injuries. Further long-term studies are needed to optimize immunosuppressive approaches and refine CNT management.
目的:钙调神经磷酸酶抑制剂(CNIs)彻底改变了移植医学,提高了同种异体移植物的存活率,但也带来了诸如钙调神经磷酸酶抑制剂诱导的肾毒性(CNT)等挑战。急性CNT通常呈剂量依赖性,会导致血管收缩和急性肾损伤,治疗重点是减少CNI暴露。慢性CNT表现为同种异体移植物功能逐渐下降,难以与非特异性同种异体移植肾病区分开来。 方法:本叙述性综述简要概述了CNT的临床管理,涵盖急性和慢性CNT。我们回顾了关于减轻CNT策略的原始文章、标志性论文和荟萃分析,包括减少CNI使用的方法。 结果:预防措施包括联合用药、监测CNI暴露以及减少CNI使用的策略,如降低目标谷浓度并转换为雷帕霉素靶蛋白抑制剂(mTORi)或贝拉西普。尽管移植物功能有所改善,但在证明减少CNI使用的方案在同种异体移植物存活方面存在显著差异方面仍存在挑战。必须牢记,随着时间的推移,慢性同种异体移植肾病的主要原因已从慢性CNT转变为免疫触发损伤和/或合并症,这些是同种异体移植物恶化的相关因素。 结论:CNIs显著改善了肾移植结果,但其相关的肾毒性需要采取减轻策略。实施此类方案的决定始终是在免疫损伤风险之间进行权衡的个人选择。需要进一步的长期研究来优化免疫抑制方法并完善CNT管理。
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