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肾移植后改用依维莫司的钙调磷酸酶抑制剂免费方案的长期结果。

Long-Term Results in Recipients of Late Conversion to a Calcineurin Inhibitor-Free Regimen with Everolimus After Kidney Transplantation.

机构信息

Department of Urology, Hokkaido University Hospital, Sapporo, Japan.

Department of Urology, Hokkaido University Hospital, Sapporo, Japan.

出版信息

Transplant Proc. 2023 May;55(4):803-808. doi: 10.1016/j.transproceed.2023.04.008. Epub 2023 May 4.

DOI:10.1016/j.transproceed.2023.04.008
PMID:37147197
Abstract

BACKGROUND

Conversion to a calcineurin inhibitor (CNI)-free regimen in cases of CNI nephrotoxicity (CNIT) is a strategy to improve the long-term outcomes of kidney transplantation. However, the long-term results of late conversion to a CNI-free regimen using everolimus (EVR) remain uncertain.

METHODS

Nine kidney transplant recipients with biopsy-confirmed CNIT were enrolled. The median time of CNIT diagnosis was 9.0 years. All recipients underwent a conversion from CNI to EVR. We evaluated the clinical outcomes, development of donor-specific antibody (DSA), the incidence of rejection, alternative arteriolar hyalinosis (aah) scores, renal function changes, and T cell responses by mixed lymphocyte reaction (MLR) assay after conversion.

RESULTS

The median follow-up after conversion was 5.4 years. Currently, 7 of 9 recipients have received a CNI-free regimen for 1.6 to 9.5 years. In the other 2 recipients, one experienced graft loss due to CNIT 3.8 years after conversion, and the other had to resume CNI due to acute T cell-mediated rejection (ATMR) a year after conversion. None of the recipients developed DSA. No rejection was observed in the kidney allograft histology except for the ATMR case. Moreover, improvement in aah scores was noted in one patient. Furthermore, serum creatinine levels were stable in recipients without proteinuria before the EVR add-on. In the MLR analysis, low responses against donors were observed in stable patients.

CONCLUSIONS

Late conversion to an EVR-based regimen without CNI may be a promising therapeutic strategy against CNIT, particularly for recipients without proteinuria before the EVR add-on.

摘要

背景

在钙调磷酸酶抑制剂(CNI)肾毒性(CNIT)的情况下转换为无 CNI 方案是改善肾移植长期结果的一种策略。然而,使用依维莫司(EVR)晚期转换为无 CNI 方案的长期结果仍不确定。

方法

纳入 9 例经活检证实为 CNIT 的肾移植受者。CNIT 诊断的中位时间为 9.0 年。所有受者均从 CNI 转换为 EVR。我们评估了临床结果、供体特异性抗体(DSA)的发展、排斥反应的发生率、替代小动脉玻璃样变(aah)评分、肾功能变化以及转换后混合淋巴细胞反应(MLR)测定的 T 细胞反应。

结果

转换后中位随访时间为 5.4 年。目前,9 例受者中有 7 例接受无 CNI 方案治疗 1.6 至 9.5 年。在另外 2 例受者中,1 例在转换后 3.8 年因 CNIT 导致移植物丢失,另 1 例在转换后 1 年因急性 T 细胞介导的排斥反应(ATMR)而不得不恢复使用 CNI。受者均未发生 DSA。除 ATMR 病例外,肾移植组织学未见排斥反应。此外,1 例患者的 aah 评分有所改善。此外,在 EVR 加用前无蛋白尿的受者中,血清肌酐水平稳定。在 MLR 分析中,稳定患者对供体的反应较低。

结论

晚期转换为无 CNI 的 EVR 方案可能是一种针对 CNIT 的有前途的治疗策略,特别是对于 EVR 加用前无蛋白尿的受者。

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