Ettenger R, Chin H, Kesler K, Bridges N, Grimm P, Reed E F, Sarwal M, Sibley R, Tsai E, Warshaw B, Kirk A D
Department of Pediatrics, University of California, Los Angeles, Los Angeles, CA.
Rho Inc, Chapel Hill, NC.
Am J Transplant. 2017 Jun;17(6):1549-1562. doi: 10.1111/ajt.14169. Epub 2017 Feb 1.
The Immune Development in Pediatric Transplantation (IMPACT) study was conducted to evaluate relationships among alloimmunity, protective immunity, immune development, physical parameters, and clinical outcome in children undergoing kidney transplantation. We prospectively evaluated biopsy-proven acute rejection (BPAR), de novo donor-specific antibody (dnDSA) formation, viremia, viral infection, T cell immunophenotyping, and body mass index (BMI)/weight Z scores in the first year posttransplantation in 106 pediatric kidney transplant recipients. Outcomes were excellent with no deaths and 98% graft survival. Rejection and dnDSAs occurred in 24% and 22%, respectively. Pretransplant cytomegalovirus (CMV) and Epstein-Barr virus (EBV) serologies and subsequent viremia were unrelated to BPAR or dnDSA. Viremia occurred in 73% of children (EBV, 34%; CMV, 23%; BMK viremia, 23%; and JC virus, 21%). Memory lymphocyte phenotype at baseline was not predictive of alloimmune complications. Patients who developed viral infection had lower weight (-2.1) (p = 0.028) and BMI (-1.2) (p = 0.048) Z scores at transplantation. The weight difference persisted to 12 months compared with patients without infection (p = 0.038). These data indicate that there is a high prevalence of viral disease after pediatric kidney transplantation, and underweight status at transplantation appears to be a risk factor for subsequent viral infection. The occurrence of viremia/viral infection is not associated with alloimmune events.
开展小儿移植免疫发育(IMPACT)研究,以评估肾移植儿童的同种免疫、保护性免疫、免疫发育、身体参数和临床结局之间的关系。我们前瞻性评估了106例小儿肾移植受者移植后第一年经活检证实的急性排斥反应(BPAR)、新生供者特异性抗体(dnDSA)形成、病毒血症、病毒感染、T细胞免疫表型分析以及体重指数(BMI)/体重Z评分。结局良好,无死亡病例,移植肾存活率为98%。排斥反应和dnDSA的发生率分别为24%和22%。移植前巨细胞病毒(CMV)和EB病毒(EBV)血清学检查及随后的病毒血症与BPAR或dnDSA无关。73%的儿童出现病毒血症(EBV,34%;CMV,23%;BK病毒血症,23%;JC病毒,21%)。基线时的记忆淋巴细胞表型不能预测同种免疫并发症。发生病毒感染的患者在移植时体重Z评分较低(-2.1)(p = 0.028),BMI Z评分较低(-1.2)(p = 0.048)。与未感染的患者相比,体重差异持续至12个月(p = 0.038)。这些数据表明,小儿肾移植后病毒疾病的患病率很高,移植时体重不足似乎是随后病毒感染的一个危险因素。病毒血症/病毒感染的发生与同种免疫事件无关。