Schotters Felicitas Leonie, Beime Jan, Briem-Richter Andrea, Binder Thomas, Herden Uta, Grabhorn Enke Freya
Department of Pediatric Hepatology and Liver Transplantation, Universitätsklinikum Hamburg-Eppendorf, Hamburg 20246, Germany.
Department of Transfusion Medicine, Human Leucocyte Antigen Laboratory, University Medicine Rostock, Rostock 18057, Germany.
World J Hepatol. 2021 Jun 27;13(6):673-685. doi: 10.4254/wjh.v13.i6.673.
In a previous paper, we reported a high prevalence of donor-specific antibody (DSA) in pediatric patients with chronic rejection and expressed the need for confirmation of these findings in a larger cohort.
To clarify the importance of DSAs on long-term graft survival in a larger cohort of pediatric patients.
We performed a retrospective analysis of 123 pediatric liver transplantation (LT) recipients who participated in yearly follow-ups including Luminex testing for DSA at our center. The cohort was split into two groups according to the DSA status (DSA-positive = 54, DSA-negative = 69). Groups were compared with regard to liver function, biopsy findings, graft survival, need for re-LT and immunosuppressive medication.
DSA-positive pediatric patients showed a higher prevalence of chronic rejection ( = 0.01), fibrosis ( < 0.001) and re-transplantation ( = 0.018) than DSA-negative patients. Class II DSAs particularly influenced graft survival. Alleles DQ2, DQ7, DQ8 and DQ9 might serve as indicators for the risk of chronic rejection and/or allograft fibrosis. Mean fluorescence intensity levels and DSA number did not impact graft survival. Previous episodes of chronic rejection might lead to DSA development.
DSA prevalence significantly affected long-term liver allograft performance and liver allograft survival in our cohort of pediatric LT. Screening for class II DSAs in combination with assessment of protocol liver biopsies for chronic antibody-mediated rejection improved early identification of patients at risk of graft loss.
在之前的一篇论文中,我们报道了慢性排斥反应的儿科患者中供体特异性抗体(DSA)的高患病率,并表示需要在更大的队列中证实这些发现。
在更大的儿科患者队列中阐明DSA对长期移植物存活的重要性。
我们对123名参与年度随访的儿科肝移植(LT)受者进行了回顾性分析,随访包括在我们中心进行的DSA的Luminex检测。根据DSA状态将队列分为两组(DSA阳性=54,DSA阴性=69)。比较两组在肝功能、活检结果、移植物存活、再次LT需求和免疫抑制药物方面的情况。
与DSA阴性患者相比,DSA阳性的儿科患者慢性排斥反应(=0.01)、纤维化(<0.001)和再次移植(=0.018)的患病率更高。II类DSA对移植物存活有特别影响。等位基因DQ2、DQ7、DQ8和DQ9可能作为慢性排斥反应和/或同种异体移植物纤维化风险的指标。平均荧光强度水平和DSA数量不影响移植物存活。既往慢性排斥反应发作可能导致DSA产生。
在我们的儿科LT队列中,DSA患病率显著影响长期肝同种异体移植物性能和肝同种异体移植物存活。筛查II类DSA并结合对慢性抗体介导排斥反应的方案肝活检评估,可改善对有移植物丢失风险患者的早期识别。