Bryan Christopher F, Harrell Kevin M, Mitchell Stanley I, Warady Bradley A, Aeder Mark I, Luger Alan M, Murillo Daniel, Muruve Nicolas A, Nelson Paul W, Shield Charles F
Midwest Transplant Network, Westwood, KS, USA.
Am J Transplant. 2003 Apr;3(4):459-64. doi: 10.1034/j.1600-6143.2003.00093.x.
The points now assigned for the quality of HLA match have received significant scrutiny to be modified in an effort to help reduce disparity in access to kidneys of minority groups, and since differences in graft survival between groups of patients in each of the HLA matched groups is less now than in the past. We analyzed long-term (5-year) graft survival in 746 DR DNA typed recipients of cadaveric kidneys transplanted from 1994-2001 whose donors were also DR DNA typed, with allocation based on those DNA-based typings. Five-year graft survival was not significantly different for recipient groups irrespective of if they had zero (84%), one (92%), two (89%), or three to four B, DR mismatches (79%) (log-rank = 0.15; died with a functioning graft [DWFG] censored). Mismatching of three and four DR and DQ antigens in black but not white patients was associated with significantly worse survival (Relative Risk = 2.9) (p = 0.002). The incidence of minority transplants in the well-matched group (zero and one B, DR mismatch), 12.8% (20/156) was over half that of the less well-matched group, 27.1% (160/590) (p < 0.001). Our data indicate that the current HLA-B, DR-based point system used to allocate kidneys warrants re-evaluation. Our data, taken in the context of the UNOS data, which has recently been re-evaluated, suggest that the only HLA-DR remain as a component of the national kidney allocation algorithm so as to increase access of kidneys to minorities and minimize graft loss.
目前为HLA配型质量所设定的分值已受到严格审查,有望进行修改,以减少少数群体在获取肾脏方面的差距,而且现在每个HLA配型组内患者群体之间的移植物存活率差异比过去要小。我们分析了1994年至2001年间接受尸体肾移植的746例进行DR DNA分型的受者的长期(5年)移植物存活率,其供者也进行了DR DNA分型,并根据这些基于DNA的分型进行分配。无论受者组的B、DR错配数为零(84%)、一个(92%)、两个(89%)还是三到四个(79%),其5年移植物存活率均无显著差异(对数秩检验=0.15;存活且移植物功能良好时死亡[DWFG]进行截尾)。黑人而非白人患者中三个和四个DR及DQ抗原错配与显著较差的存活率相关(相对风险=2.9)(p=0.002)。在配型良好组(B、DR错配数为零和一个)中,少数群体移植的发生率为12.8%(20/156),超过了配型较差组的一半,后者为27.1%(160/590)(p<0.001)。我们的数据表明,目前用于分配肾脏的基于HLA - B、DR的积分系统值得重新评估。结合最近重新评估的器官共享联合网络(UNOS)数据来看,我们的数据表明,唯一应保留作为国家肾脏分配算法组成部分的HLA - DR,以便增加少数群体获取肾脏的机会并使移植物损失最小化。