Department of Pediatrics, Harvard Medical School and Division of Endocrinology, Boston Children's Hospital, Boston, Massachusetts, USA.
Electrophysiology Facility, University of Zurich, Zurich, Switzerland.
Acta Physiol (Oxf). 2024 Dec;240(12):e14248. doi: 10.1111/apha.14248. Epub 2024 Oct 25.
Calcineurin inhibitors (CnIs) are effective immunosuppressants with decades of accumulated experience in treating immune disorders and, most notably, solid organ transplantation. While CnIs have significantly increased graft survival and transformed the patient standard of care, their use has been overshadowed by a number of undesired side effects. For instance, CnI-associated nephrotoxicity has been reported since early studies and remains a major therapeutic concern. The occurrence of several ion imbalances alongside hypertension was also noted early on, indicating the involvement of the renin-angiotensin-aldosterone system (RAAS) in CnI-mediated toxicity. However, the literature in this field is crowded with conflicting reports from clinical trials as well as studies using animal and invitro models. With this review, we aim to provide a structured and updated overview of the physiological and pathophysiological evidence supporting the involvement of the classical RAAS in CnI-associated toxicity.
钙调磷酸酶抑制剂(CNIs)是有效的免疫抑制剂,在治疗免疫紊乱方面已有数十年的经验积累,尤其是在实体器官移植方面。虽然 CnI 显著提高了移植物的存活率,并改变了患者的治疗标准,但它们的使用也带来了许多不良副作用。例如,自早期研究以来,就有报道称 CnI 相关的肾毒性仍然是一个主要的治疗关注点。此外,早期还注意到高血压伴随的几种离子失衡,这表明肾素-血管紧张素-醛固酮系统(RAAS)参与了 CnI 介导的毒性。然而,该领域的文献中充斥着来自临床试验以及使用动物和体外模型的研究的相互矛盾的报告。通过这篇综述,我们旨在提供一个结构化和更新的综述,以支持经典 RAAS 参与 CnI 相关毒性的生理和病理生理学证据。