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青少年肾移植后使用贝利尤单抗:一项回顾性研究。

Belatacept after kidney transplantation in adolescents: a retrospective study.

机构信息

Department of Pediatric Nephrology, Hannover Medical School, Hannover, Germany.

Department of Transfusion Medicine, Hannover Medical School, Hannover, Germany.

出版信息

Transpl Int. 2017 May;30(5):494-501. doi: 10.1111/tri.12932. Epub 2017 Mar 5.

Abstract

Regardless of recipient age at kidney transplantation (KTx), patients are at greatest risk for graft loss in adolescence, partly due to nonadherence to an oral immunosuppressive regimen. Belatacept, a non-nephrotoxic, first-in-class immunosuppressant that inhibits costimulation of T cells requires intravenous application only every 4 weeks, potentially leading to better adherence. However, it is only approved for use in adults. We report here the findings of the first study of belatacept in adolescents, comprising all patients in our department switched to belatacept post-KTx. Six patients (median age 15.5 years) were switched after a median of 7.5 months (range 23 days to 12 years), treatment range 3-28 months (cumulative 83 months): Three patients switched early (<3 months after KTx) had increased estimated glomerular filtration rate (GFR); one patient switched 12 years post-KTx has stable GFR; two patients were switched following rapid decline of and with markedly impaired GFR, changing slope in one patient. One patient had one acute rejection. In addition of two patients who received belatacept for other conditions, the only relevant adverse event was neutropenia (after a cumulative 109 months). Belatacept as primary immunosuppression is an option in Epstein-Barr virus-seropositive nonadherent adolescents if administered sufficiently early before deterioration of graft function.

摘要

无论受者在肾移植 (KTx) 时的年龄如何,青少年时期发生移植物丢失的风险最大,部分原因是非依从性口服免疫抑制方案。巴利昔单抗是一种非肾毒性、首创的免疫抑制剂,可抑制 T 细胞的共刺激作用,仅需每 4 周静脉应用一次,可能会提高依从性。但它仅被批准用于成人。我们在此报告了巴利昔单抗在青少年中的首次研究结果,该研究包括我们科室中所有在 KTx 后转换为巴利昔单抗的患者。6 名患者(中位年龄 15.5 岁)在 KTx 后中位时间为 7.5 个月(范围 23 天至 12 年)时转换,治疗范围为 3-28 个月(累计 83 个月):3 名患者在 KTx 后<3 个月转换,肾小球滤过率(GFR)估计值增加;1 名患者在 KTx 后 12 年时 GFR 稳定;2 名患者在 GFR 迅速下降和明显受损后转换,1 名患者的斜率发生变化。1 名患者发生 1 次急性排斥反应。除了 2 名因其他疾病接受巴利昔单抗治疗的患者外,唯一相关的不良事件是中性粒细胞减少症(累计 109 个月)。如果在移植物功能恶化之前足够早开始,巴利昔单抗作为原发性免疫抑制剂是 Epstein-Barr 病毒血清阳性不依从青少年的一种选择。

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