Department of Pediatrics, Harvard Medical School and Boston Children's Hospital, Boston, Massachusetts, USA.
Department of Pediatrics, University of Wisconsin Madison, Madison, Wisconsin, USA.
Pediatr Transplant. 2024 May;28(3):e14734. doi: 10.1111/petr.14734.
Antibody-mediated rejection (AMR) is a major cause of kidney allograft loss. There is a paucity of large-scale pediatric-specific data regarding AMR treatment outcomes.
Data were obtained from 14 centers within the Pediatric Nephrology Research Consortium. Kidney transplant recipients aged 1-18 years at transplant with biopsy-proven AMR between 2009 and 2019 and at least 12 months of follow-up were included. The primary outcome was graft failure or an eGFR <20 mL/min/1.73 m at 12 months following AMR treatment. AMR treatment choice, histopathology, and DSA class were also examined.
We reviewed 123 AMR episodes. Median age at diagnosis was 15 years at a median 22 months post-transplant. The primary outcome developed in 27.6%. eGFR <30 m/min/1.73 m at AMR diagnosis was associated with a 5.6-fold higher risk of reaching the composite outcome. There were no significant differences in outcome by treatment modality. Histopathology scores and DSA class at time of AMR diagnosis were not significantly associated with the primary outcome.
In this large cohort of pediatric kidney transplant recipients with AMR, nearly one-third of patients experienced graft failure or significant graft dysfunction within 12 months of diagnosis. Poor graft function at time of diagnosis was associated with higher odds of graft failure.
抗体介导的排斥反应(AMR)是导致肾移植失败的主要原因。目前,关于 AMR 治疗结果的大型儿科特异性数据较少。
数据来自儿科肾脏病学研究联合会的 14 个中心。纳入的患者为 2009 年至 2019 年间移植时年龄为 1-18 岁、经活检证实存在 AMR 且至少有 12 个月随访的肾移植受者。主要结局为 AMR 治疗后 12 个月时发生移植物失功或 eGFR<20ml/min/1.73m。还检查了 AMR 治疗选择、组织病理学和 DSA 分类。
我们回顾了 123 例 AMR 发作。诊断时的中位年龄为 15 岁,移植后中位数为 22 个月。主要结局的发生率为 27.6%。AMR 诊断时 eGFR<30ml/min/1.73m 与达到复合结局的风险增加 5.6 倍相关。治疗方式之间的结局无显著差异。AMR 诊断时的组织病理学评分和 DSA 分类与主要结局无显著相关性。
在本项针对患有 AMR 的大量儿科肾移植受者的研究中,近三分之一的患者在诊断后 12 个月内发生移植物失功或明显的移植物功能障碍。诊断时的移植功能不良与移植物失功的可能性增加相关。