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小儿肾移植受者的免疫抑制治疗。

Immunosuppressive Management of Pediatric Kidney Transplant Recipients.

机构信息

Department of Pediatrics and Transplantation Center, University Hospital Motol, 2nd Faculty of Medicine, Charles University Prague and Biomedical Centre, Faculty of Medicine in Plzen, Charles University Prague, Plzen, Czech Republic.

出版信息

Curr Pharm Des. 2020;26(28):3451-3459. doi: 10.2174/1381612826666200708133429.

Abstract

Kidney transplantation is a preferable treatment of children with end-stage kidney disease. All kidney transplant recipients, including pediatric need immunosuppressive medications to prevent rejection episodes and graft loss. Induction therapy is used temporarily only immediately following transplantation while maintenance immunosuppressive drugs are started and given long-term. There is currently no consensus regarding the use of induction therapy in children; its use should be decided based on the immunological risk of the child. The recent progress shows that the recommended strategy is to use as maintenance immunosuppressive therapy a combination of a calcineurin inhibitor (preferably tacrolimus) with an antiproliferative drug (preferably mycophenolate mofetil) with steroids that can be withdrawn early or late in low-risk children. The mTOR-inhibitors (sirolimus, everolimus) are used rarely in pediatrics because of common side effects and no evidence of a benefit over calcineurin inhibitors. The use of calcineurin inhibitors, mycophenolate, and mTOR-inhibitors should be followed by therapeutic drug monitoring. Immunosuppressive therapy of acute rejection consists of high-dose steroids and/or anti-lymphocyte antibodies (T-cell mediated rejection) or plasma exchange, intravenous immunoglobulines and/or rituximab (antibodymediated rejection). The future strategies for research are mainly precise characterisation of children needing induction therapy, more specific indications for mTOR-inhibitors and for the far future, the possibility to reach the immuno tolerance.

摘要

肾移植是治疗儿童终末期肾病的首选方法。所有肾移植受者,包括儿科患者,都需要免疫抑制药物来预防排斥反应和移植物丢失。诱导治疗仅在移植后立即暂时使用,而维持性免疫抑制药物则开始并长期使用。目前,对于儿童使用诱导治疗尚没有共识;其使用应根据儿童的免疫风险来决定。最近的进展表明,推荐的策略是使用钙调神经磷酸酶抑制剂(首选他克莫司)与抗增殖药物(首选霉酚酸酯)联合作为维持性免疫抑制治疗,并在低风险儿童中早期或晚期停用类固醇。由于常见的副作用和缺乏优于钙调神经磷酸酶抑制剂的证据,mTOR 抑制剂(西罗莫司、依维莫司)在儿科中很少使用。应进行治疗药物监测以监测钙调神经磷酸酶抑制剂、霉酚酸酯和 mTOR 抑制剂的使用情况。急性排斥反应的免疫抑制治疗包括大剂量类固醇和/或抗淋巴细胞抗体(T 细胞介导的排斥反应)或血浆置换、静脉注射免疫球蛋白和/或利妥昔单抗(抗体介导的排斥反应)。未来的研究策略主要是精确描述需要诱导治疗的儿童,更具体地说明 mTOR 抑制剂的适应证,以及在遥远的未来,达到免疫耐受的可能性。

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