ABO 和 HLA 不相容的肾移植的临床结果:一项全国性队列研究。
Clinical outcomes of ABO- and HLA-incompatible kidney transplantation: a nationwide cohort study.
机构信息
Transplantation Research Centre, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Division of Nephrology, Department of Internal Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
出版信息
Transpl Int. 2017 Dec;30(12):1215-1225. doi: 10.1111/tri.12979. Epub 2017 Jul 6.
This was a nationwide cohort study to investigate the impact of anti-A/B and donor-specific anti-HLA (HLA-DSA) antibodies on the clinical outcomes in kidney transplant recipients (KTRs). We classified a total of 1964 KTRs into four groups: transplants from ABO-incompatible donors (ABOi, n = 248); transplants in recipients with HLA-DSA (HLAi, n = 144); transplants from combined ABOi and HLAi donors (ABOi + HLAi, n = 31); and a control group for whom neither ABOi nor HLAi was applicable (CONT, n = 1541). We compared the incidence of biopsy-proven acute rejection (BPAR), allograft and patient survival rates. The incidence of BPAR was higher in the HLAi and ABOi + HLAi groups relative to the CONT group; in contrast, it was not higher in the ABOi group. Death-censored graft survival rates did not differ across the four groups. However, relative to the CONT group, patient survival rate was reduced in the ABOi and ABOi + HLAi groups, and with infection being the most common cause of death. Further, multivariable analysis revealed that desensitization therapy because of ABOi or HLAi was independent risk factors for patient mortality. HLAi was a more important risk factor for BPAR compared with ABOi. However, pretransplant desensitization therapy for either ABOi or HLAi significantly increased the risk of infection-related mortality.
这是一项全国性队列研究,旨在调查抗 A/B 和供体特异性抗 HLA(HLA-DSA)抗体对肾移植受者(KTR)临床结局的影响。我们将总共 1964 名 KTR 分为四组:来自 ABO 不合供体的移植(ABOi,n=248);有 HLA-DSA 的受者的移植(HLAi,n=144);来自 ABOi 和 HLAi 供体联合的移植(ABOi+HLAi,n=31);以及既无 ABOi 也无 HLAi 的对照组(CONT,n=1541)。我们比较了活检证实的急性排斥反应(BPAR)、同种异体移植物和患者生存率的发生率。与 CONT 组相比,HLAi 和 ABOi+HLAi 组的 BPAR 发生率更高;相反,ABOi 组的发生率并没有更高。死亡病例校正移植物存活率在四组之间没有差异。然而,与 CONT 组相比,ABOi 和 ABOi+HLAi 组的患者生存率降低,感染是最常见的死亡原因。此外,多变量分析显示,由于 ABOi 或 HLAi 而进行的脱敏治疗是患者死亡的独立危险因素。与 ABOi 相比,HLAi 是 BPAR 的更重要危险因素。然而,无论是 ABOi 还是 HLAi 的移植前脱敏治疗都会显著增加与感染相关的死亡率。