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托珠单抗治疗儿童肾移植受者难治性抗体介导排斥反应(AMR)的长期耐受性和临床结局。

Long term tolerability and clinical outcomes associated with tocilizumab in the treatment of refractory antibody mediated rejection (AMR) in pediatric renal transplant recipients.

机构信息

Department of Pediatrics, University of California Los Angeles, Los Angeles, California, USA.

Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California, USA.

出版信息

Clin Transplant. 2022 Aug;36(8):e14734. doi: 10.1111/ctr.14734. Epub 2022 Jun 12.

Abstract

BACKGROUND

Treatment options for antibody-mediated rejection (AMR) are limited. Recent studies have shown that inhibition of interleukin-6 (IL-6)/interleukin-6 receptor (IL-6R) signaling can reduce inflammation and slow AMR progression.

METHODS

We report our experience using monthly tocilizumab (anti-IL6R) in 25 pediatric renal transplant recipients with AMR, refractory to IVIg/Rituximab. From January 2013 to June 2019, a median (IQR) of 12 (6.019.0) doses of tocilizumab were given per patient. Serial assessments of renal function, biopsy findings, and HLA DSA (by immunodominant HLA DSA [iDSA] and relative intensity score [RIS]) were performed.

RESULTS

Median (IQR) time from transplant to AMR was 41.4 (24.367.7) months, and time from AMR to first tocilizumab was 10.6 (8.317.6) months. At median (IQR) follow up of 15.8 (8.435.7) months post-tocilizumab initiation, renal function was stable except for 1 allograft loss. There was no significant decrease in iDSA or RIS. Follow up biopsies showed reduction in peritubular capillaritis (p = .015) and C4d scoring (p = .009). The most frequent adverse events were cytopenias.

CONCLUSIONS

Tocilizumab in pediatric patients with refractory AMR was well tolerated and appeared to stabilize renal function. The utility of tocilizumab in the treatment of AMR in this population should be further explored.

摘要

背景

抗体介导的排斥反应 (AMR) 的治疗选择有限。最近的研究表明,抑制白细胞介素-6 (IL-6)/白细胞介素-6 受体 (IL-6R) 信号可以减少炎症并减缓 AMR 进展。

方法

我们报告了我们在 25 例 AMR 且对 IVIg/利妥昔单抗难治的儿科肾移植受者中使用每月托珠单抗(抗 IL-6R)的经验。从 2013 年 1 月至 2019 年 6 月,每位患者接受中位数(IQR)12(6.019.0)剂量的托珠单抗。对肾功能、活检结果和 HLA DSA(通过免疫显性 HLA DSA [iDSA] 和相对强度评分 [RIS])进行了连续评估。

结果

从移植到 AMR 的中位(IQR)时间为 41.4(24.367.7)个月,从 AMR 到首次使用托珠单抗的时间为 10.6(8.317.6)个月。在托珠单抗治疗开始后的中位(IQR)随访 15.8(8.435.7)个月时,肾功能稳定,除 1 例移植物丢失外。iDSA 或 RIS 无显著下降。随访活检显示肾小管毛细血管炎(p=0.015)和 C4d 评分(p=0.009)减少。最常见的不良事件是细胞减少症。

结论

托珠单抗在难治性 AMR 的儿科患者中耐受性良好,似乎稳定了肾功能。托珠单抗在该人群中治疗 AMR 的效用应进一步探讨。

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