Ramirez P, Chavez R, Majado M, Munitiz V, Muñoz A, Hernandez Q, Palenciano C G, Pino-Chavez G, Loba M, Minguela A, Yelamos J, Gago M R, Vizcaino A S, Asensi H, Cayuela M G, Segura B, Marin F, Rubio A, Fuente T, Robles R, Bueno F S, Sansano T, Acosta F, Rodriguez J M, Navarro F, Cabezuelo J, Cozzi E, White D J, Calne R Y, Parrilla P
Department of Surgery, University Hospital Virgen Arrixaca, Murcia, Spain.
Transplantation. 2000 Oct 15;70(7):989-98. doi: 10.1097/00007890-200010150-00001.
It is not known whether the pig liver is capable of functioning efficiently when transplanted into a primate, neither is there experience in transplanting a liver from a transgenic pigs expressing the human complement regulator human complement regulator decay accelerating factor (h-DAF) into a baboon. The objective of this study was to determine whether the porcine liver would support the metabolic functions of non-human primates and to establish the effect of hDAF expression in the prevention of hyperacute rejection of porcine livers transplanted into primates.
Five orthotopic liver xenotransplants from pig to baboon were carried out: three from unmodified pigs and two using livers from h-DAF transgenic pigs.
The three control animals transplanted with livers from unmodified pigs survived for less than 12 hr. Baboons transplanted with livers from h-DAF transgenic pigs survived for 4 and 8 days. Hyperacute rejection was not detected in the baboons transplanted with hDAF transgenic pig livers; however, it was demonstrated in the three transplants from unmodified pigs. Baboons transplanted with livers from h-DAF transgenic pigs were extubated at postoperative day 1 and were awake and able to eat and drink. In the recipients of hDAF transgenic pig livers the clotting parameters reached nearly normal levels at day 2 after transplantation and remained normal up to the end of the experiments. In these hDAF liver recipients, porcine fibrinogen was first detected in the baboon plasma 2 hr postreperfusion, and was present up to the end of the experiments. One animal was euthanized at day 8 after development of sepsis and coagulopathy, the other animal arrested at day 4, after an episode of vomiting and aspiration. The postmortem examination of the hDAF transgenic liver xenografts did not demonstrate rejection.
The livers from h-DAF transgenic pigs did not undergo hyperacute rejection after orthotopic xenotransplantation in baboons. When HAR is abrogated, the porcine liver maintains sufficient coagulation and protein levels in the baboon up to 8 days after OLT.
将猪肝移植到灵长类动物体内时,其是否能够高效发挥功能尚不清楚,而且将表达人类补体调节蛋白衰变加速因子(h-DAF)的转基因猪的肝脏移植到狒狒体内也没有相关经验。本研究的目的是确定猪肝是否能支持非人灵长类动物的代谢功能,并确定hDAF表达在预防移植到灵长类动物体内的猪肝发生超急性排斥反应中的作用。
进行了5例从猪到狒狒的原位肝异种移植:3例使用未修饰猪的肝脏,2例使用h-DAF转基因猪的肝脏。
3只接受未修饰猪肝移植的对照动物存活时间不到12小时。接受h-DAF转基因猪肝移植的狒狒分别存活了4天和8天。接受hDAF转基因猪肝移植的狒狒未检测到超急性排斥反应;然而,在3例接受未修饰猪肝移植的动物中出现了超急性排斥反应。接受h-DAF转基因猪肝移植的狒狒在术后第1天拔管,清醒且能够进食和饮水。在接受hDAF转基因猪肝移植的受体中,凝血参数在移植后第2天达到接近正常水平,并在实验结束前一直保持正常。在这些接受hDAF肝脏移植的受体中,猪纤维蛋白原在再灌注后2小时首次在狒狒血浆中被检测到,并在实验结束前一直存在。1只动物在出现败血症和凝血病后第8天实施安乐死,另1只动物在出现呕吐和误吸后第4天死亡。对hDAF转基因肝异种移植物的尸检未发现排斥反应。
h-DAF转基因猪的肝脏在狒狒原位异种移植后未发生超急性排斥反应。当超急性排斥反应被消除后,猪肝在狒狒体内可维持足够的凝血和蛋白质水平长达肝移植术后8天。