Kang Zhong-Yu, Liu Chun, Liu Wei, Li Daihong
Department of Blood Transfusion, Tianjin First Central Hospital, School of Medicine, Nankai University, Tianjin, Nankai, China.
Department of Blood Transfusion, Tianjin First Central Hospital, School of Medicine, Nankai University, Tianjin, Nankai, China.
Transpl Immunol. 2023 Dec;81:101930. doi: 10.1016/j.trim.2023.101930. Epub 2023 Sep 18.
Blood transfusion after kidney transplantation may increase the risk of sensitization and development of de novo human leukocyte antigen (HLA) donor-specific antibodies (DSAs). This study aimed to evaluate whether blood transfusion during the first year after kidney transplantation influences the development of de novo DSAs and clinical outcomes of kidney transplantation recipients.
This retrospective cohort study included nonsensitized first-time kidney transplantation recipients at Tianjin First Central Hospital from 2010 to 2022. The incidence of de novo DSA development and clinical outcomes between the groups were compared. Luminex single antigen beads were used to monitor DSAs.
Of the 538 non-HLA-sensitized kidney transplantation recipients included in the study, 164 patients who received at least one unit of leukoreduced red blood cell transfusion within the first year (the transfused group), whereas the remaining 374 patients received no blood transfusion (the non-transfused group). Our analysis showed that there was a significant difference in the development of de novo DSAs and de novo anti-class I HLA-Ab between the two groups. Indeed, the transfused recipients had a higher serum creatinine and lower estimated glomerular filtration rate (eGFR) at 1-, 6-, and 12-month (all p > 0.05) after transplantation. Futhermore, a higher incidence of CMV infection, antibody-mediated rejection (AMR), hyper acute rejection (HAR), and delayed graft function (DGF) was identified in the transfused group (all p < 0.05). The graft survival was lower in the transfused group compared with patients in the non-transfused group (P = 0.002). Blood transfusion post-transplantation was a risk factor for de novo DSAs development but not an independent predictive factor for AMR and graft loss (odds ratio = 2.064 [1.243-3.429], p = 0.005).
Our study showed that blood transfusion after transplantation is associated with the occurrence of de novo DSAs increasing an immunological risk for poor clinical outcomes for kidney transplantation recipients.
肾移植后输血可能会增加致敏风险以及产生新的人类白细胞抗原(HLA)供者特异性抗体(DSA)。本研究旨在评估肾移植后第一年输血是否会影响新DSA的产生以及肾移植受者的临床结局。
这项回顾性队列研究纳入了2010年至2022年在天津市第一中心医院接受首次肾移植的未致敏受者。比较两组中新发DSA的发生率和临床结局。采用Luminex单抗原微珠法监测DSA。
在纳入研究的538例非HLA致敏肾移植受者中,164例患者在第一年接受了至少1单位去白细胞红细胞输血(输血组),其余374例患者未输血(未输血组)。我们的分析表明,两组在新发DSA和新发抗I类HLA抗体的产生方面存在显著差异。事实上,输血受者在移植后1个月、6个月和12个月时血清肌酐更高,估计肾小球滤过率(eGFR)更低(所有p>0.05)。此外,输血组中巨细胞病毒感染、抗体介导的排斥反应(AMR)、超急性排斥反应(HAR)和移植肾功能延迟恢复(DGF)的发生率更高(所有p<0.05)。与未输血组患者相比,输血组的移植物存活率更低(P=0.002)。移植后输血是新发DSA产生的危险因素,但不是AMR和移植物丢失的独立预测因素(比值比=2.064[1.243 - 3.429],p=0.005)。
我们的研究表明,移植后输血与新发DSA的发生相关,增加了肾移植受者临床结局不良的免疫风险。