Sidney∼Kimmel Comprehensive Cancer Research Center, Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Bloomberg∼Kimmel Institute for Cancer Immunotherapy, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Front Immunol. 2020 Apr 9;11:572. doi: 10.3389/fimmu.2020.00572. eCollection 2020.
Transplant tolerance in the absence of long-term immunosuppression has been an elusive goal for solid organ transplantation. Recently, it has become clear that metabolic reprogramming plays a critical role in promoting T cell activation, differentiation, and function. Targeting metabolism can preferentially inhibit T cell effector generation while simultaneously promoting the generation of T regulatory cells. We hypothesized that costimulatory blockade with CTLA4Ig in combination with targeting T cell metabolism might provide a novel platform to promote the induction of transplant tolerance.
在实体器官移植中,实现无需长期免疫抑制的移植耐受一直是一个难以企及的目标。最近,人们已经清楚地认识到,代谢重编程在促进 T 细胞激活、分化和功能方面起着关键作用。靶向代谢可以优先抑制 T 细胞效应器的产生,同时促进 T 调节细胞的产生。我们假设,使用 CTLA4Ig 进行共刺激阻断联合靶向 T 细胞代谢可能提供一个新的平台,以促进移植耐受的诱导。