Eurotransplant Reference Laboratory, Leiden University Medical Center, Leiden, the Netherlands.
Eurotransplant Reference Laboratory, Leiden University Medical Center, Leiden, the Netherlands.
Kidney Int. 2018 Feb;93(2):491-500. doi: 10.1016/j.kint.2017.07.018. Epub 2017 Sep 22.
Highly sensitized renal transplant candidates accumulate on transplant waiting lists since they produce antibodies to many HLA antigens, which in this way become unacceptable. Organ allocation to these patients is usually based on avoiding transplantation of organs bearing these unacceptable antigens. In contrast, allocation through the Eurotransplant Acceptable Mismatch (AM) program is based on extension of the patient's own HLA type with so-called acceptable HLA antigens to which strictly no antibodies are formed, as shown by extensive laboratory testing. We questioned which type of allocation results in the best long-term graft survival. Therefore, we selected 58,727 cadaveric single renal transplant recipients transplanted within Eurotransplant between 1996 and 2015 and determined factors influencing graft survival for patients transplanted through the AM program. Next, we compared ten-year graft survival of patients with various sensitization grades who received a renal transplant through regular allocation to that of highly sensitized patients transplanted through the AM program. Unlike regular allocation, no effect for HLA mismatches existed for AM patients, while factors that did affect graft survival were similar to those of the general kidney transplant population. AM patients had significantly superior ten-year graft survival compared to highly sensitized patients transplanted on the basis of avoidance of unacceptable mismatches. Strikingly, graft survival of AM patients receiving a repeat transplant was similar to that of nonsensitized repeat transplant recipients. Thus, allocation of kidneys to highly sensitized patients based on proven acceptable antigens results in a significantly better graft survival compared to mere avoidance of unacceptable mismatches.
高度致敏的肾移植候选者在移植等待名单上积累,因为他们产生针对许多 HLA 抗原的抗体,这些抗原因此变得不可接受。这些患者的器官分配通常基于避免移植携带这些不可接受抗原的器官。相比之下,通过 Eurotransplant 可接受的错配 (AM) 计划进行分配是基于扩展患者自身的 HLA 类型,带有所谓的可接受的 HLA 抗原,这些抗原严格来说不会形成抗体,这已通过广泛的实验室测试证明。我们质疑哪种分配类型会导致最佳的长期移植物存活率。因此,我们选择了 1996 年至 2015 年期间在 Eurotransplant 进行的 58,727 例尸体单肾移植受者,并确定了通过 AM 计划进行移植的患者影响移植物存活率的因素。接下来,我们比较了通过常规分配接受肾移植的不同致敏等级患者与通过 AM 计划进行移植的高度致敏患者的十年移植物存活率。与常规分配不同,AM 患者的 HLA 错配对移植物存活率没有影响,而影响移植物存活率的因素与一般肾移植人群相似。与基于避免不可接受错配的高度致敏患者进行移植相比,AM 患者的十年移植物存活率明显更高。值得注意的是,接受重复移植的 AM 患者的移植物存活率与非致敏重复移植受者相似。因此,基于已证明的可接受抗原分配肾脏给高度致敏的患者,与仅仅避免不可接受的错配相比,会导致明显更好的移植物存活率。