Pig-to-human kidney transplantation using brain-dead donors as recipients: One giant leap, or only one small step for transplantkind?

被引:7
|
作者
Ganchiku, Yoshikazu [1 ]
Riella, Leonardo V. [1 ,2 ]
机构
[1] Harvard Med Sch, Massachusetts Gen Hosp, Dept Surg, Ctr Transplantat Sci, Boston, MA 02115 USA
[2] Harvard Med Sch, Massachusetts Gen Hosp, Div Nephrol, Boston, MA 02115 USA
关键词
immunosuppression; rejection; xenotransplantation; GENETICALLY-ENGINEERED PIGS; ENDOGENOUS RETROVIRUS; HEART-TRANSPLANTATION; HUMAN THROMBOMODULIN; GRAFT-SURVIVAL; CELLS; XENOTRANSPLANTATION; INFECTION; BABOON;
D O I
10.1111/xen.12748
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
Pig kidney xenotransplantation is increasingly regarded as a realistic solution to the current shortage of human organ donors for patients with end-stage organ failure. Recently, the news of three pig-to-human transplantation cases has awakened public interest. Notably, the case by the Alabama team reported detailed and important findings for the xenotransplantation field. Using a genetically modified pig, two porcine kidneys were transplanted into a brain-dead recipient. They applied several approaches established in the preclinical NHP study, including gene-edited pig kidney graft and preoperative laboratory inspection such as crossmatching and infection screening. The pig-to-human kidney xenotransplantation had no unexpected events during surgery or evidence of hyperacute rejection. Unfortunately, the grafts did not work appropriately, and the study had to be terminated due to the decompensation of the recipient. While this study demonstrated the outstanding achievement in this research area, it also revealed remaining gaps to move xenotransplantation to the clinic. While brain-dead human recipients could reinforce the compatibility achievements of gene-edited pigs in NHP, their pro-inflammatory and pro-coagulant environment, in combination with short-duration of experiments will limit the assessment of kidney function, infection and rejection risk post-transplant, in particular antibody-mediated rejection. The use of successful immunosuppressive protocols of non-human primates xenotransplant experiments including anti-CD154 antibody will be critical to maximize the success in the first in-human trials.
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页数:6
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