C1-inhibitor for treatment of acute vascular xenograft rejection in cynomolgus recipients of h-DAF transgenic porcine kidneys

被引:29
作者
Vangerow, B [1 ]
Hecker, JM [1 ]
Lorenz, R [1 ]
Loss, M [1 ]
Przemeck, M [1 ]
Appiah, R [1 ]
Schmidtko, J [1 ]
Jalali, A [1 ]
Rueckoldt, H [1 ]
Winkler, M [1 ]
机构
[1] Hannover Med Sch, Viszeral & Transplantat Chirurg Klin, Dept Anesthesiol, D-30625 Hannover, Germany
关键词
complement; in vivo animal models; nonhuman primate; transplantation; transgenic;
D O I
10.1034/j.1399-3089.2001.00130.x
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
At present, the major barrier to successful discordant xenotransplantation of unmodified or complement regulator transgenic porcine xenografts is acute vascular xenograft rejection (AVR). AVR is associated with the intragraft deposition of induced recipient xenoreactive antibodies and subsequent complement activation. In a life-supporting pig to primate kidney xenotransplantation setting using hDAF transgenic donor organs and postoperative immunosuppression. episodes of AVR were either treated with boluses of cyclophosphamide and steroids or with the same regimen supplemented by a three-day course of C1-Inhibitor, a multifunctional complement regulator. In 8 Out of 10 animals stable initial graft function was achieved; in all animals one or more episodes of AVR were observed. When, in 4 animals, Cl-Inhibitor was added to the standard anti-rejection treatment regimen I AVR was successfully reversed in 6 out of 7 episodes, while in another group of 4 animals receiving the standard anti-rejection treatment 0 Out of 4 episodes of AVR responded to treatment. Response to anti-rejection treatment was associated with a significant increase in recipient survival time. We conclude that AVR of h-DAF transgenic porcine kidneys can be Successfully treated by additional short-tel-In fluid phase complement inhibition.
引用
收藏
页码:266 / 272
页数:7
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