免疫原性
溶血
生物
红细胞
免疫学
转基因
输血
免疫系统
基因
遗传学
作者
Yevgen Chornenkyy,Takayuki Yamamoto,Hidetaka Hara,Sean R. Stowell,Ionita Ghiran,Simon C. Robson,David K. C. Cooper
出处
期刊:Blood Reviews
[Elsevier]
日期:2023-07-14
卷期号:61: 101113-101113
被引量:2
标识
DOI:10.1016/j.blre.2023.101113
摘要
Transfusion of allogeneic human red blood cell (hRBCs) is limited by supply and compatibility between individual donors and recipients. In situations where the blood supply is constrained or when no compatible RBCs are available, patients suffer. As a result, alternatives to hRBCs that complement existing RBC transfusion strategies are needed. Pig RBCs (pRBCs) could provide an alternative because of their abundant supply, and functional similarities to hRBCs. The ability to genetically modify pigs to limit pRBC immunogenicity and augment expression of human 'protective' proteins has provided major boosts to this research and opens up new therapeutic avenues. Although deletion of expression of xenoantigens has been achieved in genetically-engineered pigs, novel genetic methods are needed to introduce human 'protective' transgenes into pRBCs at the high levels required to prevent hemolysis and extend RBC survival in vivo. This review addresses recent progress and examines future prospects for clinical xenogeneic pRBC transfusion.
科研通智能强力驱动
Strongly Powered by AbleSci AI