异种移植
同种异体移植
免疫学
细胞疗法
医学
免疫抑制
T细胞
调节性T细胞
移植
免疫系统
生物
细胞
白细胞介素2受体
内科学
遗传学
作者
Raphaël Porret,Erica Lana,Antonio Mancarella,Philippe Guillaume,Manuel Pascual,Raphaël Meier,Jonathan S. Bromberg,Muhammad M. Mohiuddin,L. Bühler,Qizhi Tang,Yannick D. Müller
标识
DOI:10.3389/fimmu.2025.1685682
摘要
Xenotransplantation has experienced major clinical advancements over the past three years. Yet, despite potent immunosuppressive regimens combining B-cell depleting therapies, T cell activation blockade, complement inhibition, and high-dose steroids, signs of antibody-mediated and cellular rejection were seen in the few pig-to human heart and kidney xenotransplants. Considering the recent success of chimeric antigen receptor T cell therapies in severe refractory autoimmune diseases, there are windows for opportunities to develop novel approaches to reduce the burden of immunosuppression. In this line, regulatory T cell (Treg) therapy is an attractive strategy, as Tregs could be genetically modified to recognize pig organs. In this brief review, we summarize the lessons learned from Tregs therapies in allotransplantation, update on the recent development in Treg research for xenotransplantation, and discuss future perspectives of humanizing pigs with human leukocyte antigens to promote tolerance using engineered Tregs.
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