Christiaans M H, Overhof R, ten Haaft A, Nieman F, van Hooff J P, van den Berg-Loonen E M
Department of Internal Medicine, University Hospital Maastricht, The Netherlands.
Transplantation. 1996 Nov 15;62(9):1341-7. doi: 10.1097/00007890-199611150-00028.
The effect of flow cytometry crossmatches on clinical outcome was studied retrospectively in two groups of immunologically well-documented patients who had received transplants with a negative complement-dependent cytotoxicity crossmatch. The first group consisted of 114 consecutive renal allograft recipients, and the second group consisted of 76 immunologically at-risk recipients. Flow cytometry crossmatches were performed with current and historic sera. In group 1, positive flow cytometry (FC) crossmatches were shown in 15/114 (13%) recipients. Rejection occurred in 8/15 (53%) FC-positive versus 41/99 (41%) FC-negative recipients. The 1-year graft survival rate was 80% for FC-positive patients and 87% for FC-negative patients. Sixty-seven patients were nonsensitized patients; 4 of them had a positive FC crossmatch but no rejection episodes, graft loss, or patient loss. Of 47 retransplanted and/or sensitized recipients, 11 had a positive FC crossmatch. Rejection treatment was needed in 8/11 (73%) FC-positive patients compared with 19/36 (53%) FC-negative patients. Their 1-year graft survival rates were 73% and 81%. None of these differences reached statistical significance. Group 2 consisted of 76 at-risk recipients; 37 were retransplant patients and 39 were sensitized first-transplant patients. Twenty-one (28%) patients showed a positive FC crossmatch. Rejection episodes did not differ between the FC-positive (48%) and FC-negative patients (46%). There was no difference in 1-year graft survival rate (76% vs. 80%) or in 1-year patient survival rate (100% vs. 95%). We conclude that FC crossmatches in our patient group are not superior to the classical complement-dependent cytotoxicity crossmatches with regard to clinical outcome. On the contrary, transplantation with a mandatory negative FC crossmatch would have excluded 28% of the recipients from transplantation, who in fact are doing well.
在两组免疫情况记录完备且补体依赖细胞毒性交叉配型为阴性的移植患者中,对流式细胞术交叉配型对临床结局的影响进行了回顾性研究。第一组由114例连续的肾移植受者组成,第二组由76例免疫高危受者组成。使用当前和既往血清进行流式细胞术交叉配型。在第一组中,114例受者中有15例(13%)显示流式细胞术(FC)交叉配型阳性。FC阳性受者中有8例(53%)发生排斥反应,而FC阴性受者中有41例(41%)发生排斥反应。FC阳性患者的1年移植存活率为80%,FC阴性患者为87%。67例患者为非致敏患者;其中4例FC交叉配型阳性,但未发生排斥反应、移植肾丢失或患者死亡。在47例再次移植和/或致敏受者中,11例FC交叉配型阳性。FC阳性患者中有8例(73%)需要进行排斥反应治疗,而FC阴性患者中有19例(53%)需要治疗。他们的1年移植存活率分别为73%和81%。这些差异均未达到统计学意义。第二组由76例高危受者组成;37例为再次移植患者,39例为致敏首次移植患者。21例(28%)患者显示FC交叉配型阳性。FC阳性患者(48%)和FC阴性患者(46%)的排斥反应发生率无差异。1年移植存活率(76%对80%)或1年患者存活率(100%对95%)无差异。我们得出结论,就临床结局而言,我们患者组中的FC交叉配型并不优于经典的补体依赖细胞毒性交叉配型。相反,强制要求FC交叉配型为阴性进行移植会使28%的受者被排除在移植之外,但实际上他们情况良好。