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诊断为移植后淋巴增殖性疾病后维持钙调磷酸酶抑制可改善肾移植物的存活率。

Maintaining calcineurin inhibition after the diagnosis of post-transplant lymphoproliferative disorder improves renal graft survival.

机构信息

Hospices Civils de Lyon, Hôpital Edouard Herriot, Service de Transplantation, Néphrologie et Immunologie Clinique, Lyon, France.

Service de Transplantation Rénale et de Soins Intensifs, Hôpital Necker, APHP, Paris, France.

出版信息

Kidney Int. 2014 Jan;85(1):182-90. doi: 10.1038/ki.2013.253. Epub 2013 Jun 26.

Abstract

Post-transplant lymphoproliferative disorder (PTLD) is an uncontrolled proliferation of transformed lymphocytes fostered by immunosuppression. In addition to chemotherapy, treatment of PTLD includes a reduction of maintenance immunosuppression. Patients with PTLD have an increased risk of graft loss, suggesting that reduced immunosuppression strategy needs to be optimized with regard to graft outcome. Here we retrospectively reviewed 101 cases involving PTLD to identify the risks associated with graft loss. During a median follow-up of 70 months, 39 patients died and 21 lost their graft. Multivariate analysis found that an eGFR under 30 ml/min per 1.73 m(2) at PTLD diagnosis, a biopsy-proven acute rejection episode following reduction of immunosuppression, and the absence of calcineurin inhibition in maintenance immunosuppression are independent risk factors for allograft loss. Neither the type of PTLD nor the chemotherapy regimen was predictive of allograft failure. Histological analysis of graft biopsies showed that maintaining calcineurin inhibition after the diagnosis of PTLD reduced the risk of developing de novo anti-HLA antibodies and humoral rejection. Remarkably, calcineurin inhibitor maintenance was neither associated with higher mortality nor with worse progression-free survival. Thus, maintaining calcineurin inhibition at a reduced dose after the diagnosis of PTLD seems safe and may improve renal graft outcome, possibly through better control of the recipient's humoral immune response.

摘要

移植后淋巴组织增生性疾病(PTLD)是一种由免疫抑制引起的转化淋巴细胞不受控制的增殖。除了化疗外,PTLD 的治疗还包括减少维持性免疫抑制。PTLD 患者移植物丢失的风险增加,这表明需要针对移植物结局优化减少免疫抑制策略。在这里,我们回顾性分析了 101 例涉及 PTLD 的病例,以确定与移植物丢失相关的风险。在中位随访 70 个月期间,39 例患者死亡,21 例患者移植物丢失。多变量分析发现,PTLD 诊断时 eGFR 低于 30ml/min/1.73m(2)、减少免疫抑制后活检证实急性排斥反应发作以及维持性免疫抑制中缺乏钙调神经磷酸酶抑制剂是移植物丢失的独立危险因素。PTLD 的类型和化疗方案均不能预测移植物失败。移植物活检的组织学分析表明,PTLD 诊断后维持钙调神经磷酸酶抑制剂可降低新出现的 HLA 抗体和体液排斥反应的风险。值得注意的是,钙调神经磷酸酶抑制剂维持既与更高的死亡率无关,也与更差的无进展生存率无关。因此,PTLD 诊断后维持低剂量钙调神经磷酸酶抑制剂似乎是安全的,并可能通过更好地控制受者的体液免疫反应来改善肾移植物结局。

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