Schuurman Henk-Jan, Pino-Chavez Gilda, Phillips M James, Thomas Lucy, White David J G, Cozzi Emanuele
Imutran Ltd (A Novartis Pharma AG Company), Cambridge, United Kingdom.
Transplantation. 2002 Apr 15;73(7):1146-51. doi: 10.1097/00007890-200204150-00024.
Cynomolgus monkeys or baboons received under immunosuppression kidney or heart grafts from pigs transgenic for human decay-accelerating factor (hDAF) or from control pigs. Hyperacute rejection (HAR) is often difficult to differentiate from nonimmunological causes of organ or recipient dysfunction (NIC), and therefore, a thorough pathology review of all cases with 0-4 days survival (inclusive) was conducted.
Pathology slides were blinded and together with limited clinical data reviewed by two pathologists. After unblinding, data were compared with the original diagnosis made during the course of the program, and a final diagnosis was reached considering the complete clinical dataset.
Life-supporting kidney transplantation was performed in 245 cynomolgus monkeys (234 hDAF, 11 controls), of which 102 cases had 0-4 day survival. None of the hDAF cases showed HAR, whereas this occurred in 27% of controls (P<10-6). Heterotopic heart transplantation was performed in 65 monkeys (57 hDAF, 8 controls), of which 41 cases had 0-4 day survival. HAR was observed in 7% of hDAF cases and in 57% of controls (P=0.002). Heterotopic heart transplantation in baboons was performed in 33 animals (28 hDAF, 5 controls), of which 15 cases had 0-4 day survival. HAR was observed in 11% of hDAF cases and in 20% of controls. Sixteen baboons were subjected to orthotopic heart transplantation, all from hDAF donors, out of which eight survived 0-4 days. The incidence of HAR was 6%.
In the largest series of pig-to-primate solid organ transplants performed thus far, the presence of the hDAF transgene fully prevents HAR of cynomolgus monkey kidney transplants and partially inhibits HAR of heart grafts in cynomolgus monkeys or baboons. The incidence of HAR in control grafts is significantly higher.
食蟹猴或狒狒在免疫抑制状态下接受来自转人衰变加速因子(hDAF)基因猪或对照猪的肾脏或心脏移植。超急性排斥反应(HAR)常常难以与器官或受体功能障碍的非免疫性原因(NIC)相区分,因此,对所有存活0至4天(含)的病例进行了全面的病理学检查。
病理切片不记名,由两位病理学家结合有限的临床数据进行检查。解除盲法后,将数据与项目过程中最初的诊断结果进行比较,并结合完整的临床数据集得出最终诊断。
对245只食蟹猴(234只接受hDAF移植,11只接受对照移植)进行了维持生命的肾脏移植,其中102例存活0至4天。接受hDAF移植的病例均未出现HAR,而对照移植组中出现HAR的比例为27%(P<10-6)。对65只猴子(57只接受hDAF移植,8只接受对照移植)进行了异位心脏移植,其中41例存活0至4天。接受hDAF移植的病例中观察到7%出现HAR,对照移植组中这一比例为57%(P=0.002)。对33只狒狒进行了异位心脏移植(28只接受hDAF移植,5只接受对照移植),其中15例存活0至4天。接受hDAF移植的病例中观察到11%出现HAR,对照移植组中这一比例为20%。16只狒狒接受了原位心脏移植,均来自hDAF供体,其中8只存活0至4天。HAR的发生率为6%。
在迄今为止进行的最大规模的猪到灵长类动物实体器官移植系列研究中,hDAF转基因的存在完全预防了食蟹猴肾脏移植的HAR,并部分抑制了食蟹猴或狒狒心脏移植的HAR。对照移植中HAR的发生率显著更高。