Claas Frans H J, Witvliet Marian D, Duquesnoy René J, Persijn Guido G, Doxiadis Ilias I N
Department of Immunohematology and Blood Transfusion, Section Immunogenetics and Transplantation Immunology, Leiden University Medical Center, Albinusdreef 2, 2333 ZA Leiden, The Netherlands.
Transplantation. 2004 Jul 27;78(2):190-3. doi: 10.1097/01.tp.0000129260.86766.67.
There are many highly sensitized patients on the kidney waiting lists of organ exchange organizations because it is difficult to find a crossmatch negative cadaver kidney for these patients. Recently, several protocols have been developed to remove the donor-specific human leukocyte antigen (HLA) antibodies from the serum of these patients before transplantation. These approaches, including the use of intravenous immunoglobulins, plasmapheresis and immunoglobulins (plasmapheresis-cytomegalovirus-immunoglobulin), and immunoabsorption, seem to lead to a certain success rate, although the additional immunosuppression necessary to remove and control the production of donor-specific alloantibodies may have its impact on the short-term (infections) and long-term (incidence of cancer) immune surveillance. Furthermore, some of these therapies represent a considerable financial burden for patients and society. In the present report, we advocate selection of crossmatch negative donors on the basis of the Acceptable Mismatch Program, as the first and best option for highly sensitized patients to undergo transplantations. No additional immunosuppression is necessary, and graft survival in this group of "difficult" patients is identical to that of nonsensitized recipients. Because the nature of the HLA polymorphism does not allow all patients to profit from this approach, removal of circulating HLA antibodies can be considered as a rescue therapy for those patients for whom the Acceptable Mismatch Program does not give a solution.
在器官交换组织的肾脏等待名单上有许多高敏患者,因为很难为这些患者找到交叉配型阴性的尸体肾。最近,已经开发了几种方案,用于在移植前从这些患者的血清中去除供体特异性人类白细胞抗原(HLA)抗体。这些方法,包括使用静脉注射免疫球蛋白、血浆置换和免疫球蛋白(血浆置换-巨细胞病毒-免疫球蛋白)以及免疫吸附,似乎取得了一定的成功率,尽管去除和控制供体特异性同种抗体产生所需的额外免疫抑制可能会对短期(感染)和长期(癌症发病率)免疫监测产生影响。此外,这些疗法中的一些对患者和社会来说是相当大的经济负担。在本报告中,我们主张根据可接受错配方案选择交叉配型阴性的供体,作为高敏患者进行移植的首要也是最佳选择。无需额外的免疫抑制,并且这组“困难”患者的移植物存活率与非致敏受者相同。由于HLA多态性的性质不允许所有患者从这种方法中获益,对于那些可接受错配方案无法解决问题的患者,可以考虑去除循环中的HLA抗体作为一种挽救疗法。