Five-Year Outcomes in Living Donor Kidney Transplants With a Positive Crossmatch

Five-Year Outcomes in Living Donor Kidney Transplants With a Positive Crossmatch
复制标题

DOI:
10.1111/j.1600-6143.2012.04291.x
复制
发表时间:
2013-01-01
影响因子:
8.8
通讯作者:
Stegall, M. D.
Stegall, M. D.
中科院分区:
医学2区
文献类型:
--
作者:
Bentall, A.;Cornell, L. D.;Stegall, M. D.

文献摘要

被引文献

相似文献

具有高水平供体特异性抗HLA抗体的肾移植候选者具有低移植率和高透析死亡率。使用脱敏方案,阳性交叉配型肾移植(+XMKTx)可能会产生良好的短期结果,但缺乏长期结果数据。本研究的目的是确定+XMKTx的实际5年移植结局。我们比较了年龄和性别匹配的102 +XMKTx和204 -XMKTx的移植物存活率和功能及组织学状态。+XMKTx组中实际5年死亡删失移植物存活率较低(70.7%对88.0%,p < 0.01),54.5%的存活移植物存在慢性损伤(肾小球病)。移植物存活率在仅具有抗供体I类抗体的受体中高于抗II类抗体(单独或与I类抗体组合)(85.3%对62.6%,p = 0.05),并且与-XMKTx相似(85.3%对88.0%,p = 0.64)。所有组的肾功能和蛋白尿范围广泛,反映了5年时不同的组织学结果。我们得出结论,当与-XMKTx相比,+XMKTx在5年时具有较差的结局,然而,几乎一半的存活移植物没有肾小球病,避免针对供体II类的抗体可能会改善结局。
Renal transplant candidates with high levels of donor-specific anti-HLA antibodies have low transplantation rates and high mortality rates on dialysis. Using desensitization protocols, good short-term outcomes are possible in positive crossmatch kidney transplants (+XMKTx), but long-term outcome data are lacking. The aim of the current study was to determine actual 5-year graft outcomes of +XMKTx. We compared graft survival and the functional and histologic status of 102 +XMKTx to 204 -XMKTx matched for age and sex. Actual 5-year death-censored graft survival was lower in the +XMKTx group (70.7% vs. 88.0%, p < 0.01) and chronic injury (glomerulopathy) was present in 54.5% of surviving grafts. Graft survival was higher in recipients with antibody against donor class I only compared with antibody against class II (either alone or in combination with class I) (85.3% vs. 62.6%, p = 0.05) and was similar to -XMKTx (85.3 vs. 88.0%, p = 0.64). Renal function and proteinuria ranged across a wide spectrum in all groups reflecting the different histological findings at 5 years. We conclude that when compared to -XMKTx, +XMKTx have inferior outcomes at 5 years, however, almost half of the surviving grafts do not have glomerulopathy and avoiding antibodies against donor class II may improve outcomes.