Newland David M, Royston Macy J, McDonald Derry R, Nemeth Thomas L, Wallace-Boughter Kelly, Carlin Kristen, Horslen Simon
Department of Pharmacy, Seattle Children's Hospital, Seattle, WA, USA.
School of Pharmacy, University of Washington, Seattle, WA, USA.
Pediatr Transplant. 2019 Dec;23(8):e13573. doi: 10.1111/petr.13573. Epub 2019 Sep 12.
Literature is limited comparing induction immunosuppression in pediatric liver transplant (LTx) recipients. This is a single-center, retrospective cohort study of primary pediatric liver transplants at our center between 2005 and 2016 who received either basiliximab (BSX) or rabbit anti-thymocyte globulin (rATG) induction. Maintenance immunosuppression consisted of tacrolimus ± a corticosteroid taper. Exclusions included receipt of an ABO-incompatible graft, retransplantation, and multi-organ transplantation. Primary outcomes were incidence of treated biopsy-proven acute rejection (tBPAR) and PTLD within the first year and infections within 90 days of LTx. Secondary outcomes included graft and patient survival, time to first tBPAR, and incidence of steroid-resistant rejection (SRR) within the first year post-LTx. A total of 136 patients were included in the final analysis of which 57 patients (42%) received BSX induction. Patients who received rATG induction with or without a 2-week corticosteroid taper experienced significantly more tBPAR compared to those who received BSX induction with a 6-month corticosteroid taper (55.7% vs 33.3%, P = .01). There were no differences in the incidence of PTLD, infections, SRR, graft or patient survival, or time to first tBPAR between the two groups. Induction with rATG either with or without a short corticosteroid taper was associated with significantly more tBPAR in primary pediatric LTx recipients when compared to BSX induction with a prolonged corticosteroid taper in the setting of maintenance immunosuppression with tacrolimus.
关于小儿肝移植(LTx)受者诱导免疫抑制的文献有限。这是一项单中心回顾性队列研究,研究对象为2005年至2016年间在本中心接受初次小儿肝移植且接受巴利昔单抗(BSX)或兔抗胸腺细胞球蛋白(rATG)诱导治疗的患者。维持免疫抑制方案为他克莫司±逐渐减量的皮质类固醇。排除标准包括接受ABO血型不相合移植物、再次移植和多器官移植。主要结局为治疗性活检证实的急性排斥反应(tBPAR)的发生率、移植后第一年的移植后淋巴组织增生性疾病(PTLD)以及肝移植后90天内的感染。次要结局包括移植物和患者生存率、首次发生tBPAR的时间以及肝移植后第一年的激素抵抗性排斥反应(SRR)发生率。最终分析共纳入136例患者,其中57例(42%)接受BSX诱导治疗。与接受6个月皮质类固醇逐渐减量的BSX诱导治疗的患者相比,接受rATG诱导治疗(无论是否联合2周皮质类固醇逐渐减量)的患者发生tBPAR的比例显著更高(55.7%对33.3%,P = 0.01)。两组在PTLD、感染、SRR、移植物或患者生存率以及首次发生tBPAR的时间方面无差异。在使用他克莫司进行维持免疫抑制的情况下,与接受延长皮质类固醇逐渐减量的BSX诱导治疗相比,接受rATG诱导治疗(无论是否联合短期皮质类固醇逐渐减量)的小儿肝移植初治受者发生tBPAR的比例显著更高。