Holt D Byron, Lublin Douglas M, Phelan Donna L, Boslaugh Sarah E, Gandhi Sanjiv K, Huddleston Charles B, Saffitz Jeffrey E, Canter Charles E
Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
J Heart Lung Transplant. 2007 Sep;26(9):876-82. doi: 10.1016/j.healun.2007.07.011.
The difficulty in obtaining a prospective negative donor/recipient crossmatch limits the ability to successfully transplant pediatric heart transplant candidates who show evidence of antibodies to multiple human leukocyte antigens (pre-sensitized patients).
We utilized a protocol that included peri-operative plasmapheresis, thymoglobulin and cyclophosphamide in 17 pre-sensitized (panel-reactive antibodies [PRA] >10%) pediatric patients to accept donors for these patients without a prospective crossmatch between 1995 and 2005. A retrospective review of survival, rejection and infection was performed, comparing the frequency of rejection and infection in our patients who were transplanted with a complement-dependent cytotoxic (CDC)-positive donor/recipient crossmatch to those patients transplanted with a negative crossmatch.
Thirteen of 17 patients were found to have a CDC-positive crossmatch. Actuarial survival after transplantation was 85% at 1 year and 73% at 3 years. Twelve of 13 (92%) of these patients experienced rejection, and 5 of 13 (38%) had recurrent rejection, generally in the first 2 months after transplantation. Rejection was associated with hemodynamic compromise in 58% of first rejection episodes and 67% of episodes of recurrent rejection. The frequency of rejection in these patients was significantly greater than the frequency in patients with a negative crossmatch in the first 6 months after transplantation, but not afterward. The frequency of infection episodes was not significantly different between the groups.
Heart transplantation in pre-sensitized pediatric recipients with a CDC-positive donor/recipient crossmatch may result in reasonable short-term survival, but with a high frequency of early rejection, often with hemodynamic compromise.
获得前瞻性阴性供体/受体交叉配型存在困难,这限制了成功移植那些显示出针对多种人类白细胞抗原具有抗体证据的小儿心脏移植候选者(预致敏患者)的能力。
我们采用了一种方案,该方案包括在1995年至2005年期间,对17例预致敏(群体反应性抗体[PRA]>10%)的小儿患者进行围手术期血浆置换、抗胸腺细胞球蛋白和环磷酰胺治疗,以使这些患者在没有前瞻性交叉配型的情况下接受供体。对生存、排斥反应和感染情况进行了回顾性分析,比较了接受补体依赖细胞毒性(CDC)阳性供体/受体交叉配型移植的患者与接受阴性交叉配型移植的患者的排斥反应和感染频率。
17例患者中有13例被发现交叉配型为CDC阳性。移植后的1年实际生存率为85%,3年为73%。这些患者中有12例(92%)发生了排斥反应,13例中有5例(38%)出现反复排斥反应,通常发生在移植后的前2个月。58%的首次排斥反应发作和67%的反复排斥反应发作与血流动力学损害有关。这些患者在移植后的前6个月内排斥反应的频率明显高于交叉配型为阴性的患者,但之后则无明显差异。两组之间感染发作的频率没有显著差异。
对于交叉配型为CDC阳性的预致敏小儿受体进行心脏移植可能会带来合理的短期生存,但早期排斥反应的频率较高,且常伴有血流动力学损害。