Hong Zixuan, Zhao Yun, Pahlavan Sara, Wang Xue, Han Sen, Wang Xi, Wang Kai
Department of Physiology and Pathophysiology, School of Basic Medical Sciences, State Key Laboratory of Vascular Homeostasis and Remodeling, Beijing Advanced Center of Cellular Homeostasis and Aging-Related Diseases, Clinical Stem Cell Research Center, Peking University Third Hospital, Peking University, Beijing 100191, China.
Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran 16635-148, Iran.
Life Med. 2025 Mar 31;4(3):lnaf016. doi: 10.1093/lifemedi/lnaf016. eCollection 2025 Jun.
Human pluripotent stem cells (hPSCs) hold great promise in regenerative medicine. However, immune rejections remain one of the major obstacles to stem cell therapy. Though conventional immunosuppressants are available in clinics, the side effects prevent the wide application of hPSCs derivatives, compromising both survival rate and quality of life. In recent years, a myriad of strategies aimed at inducing immune tolerance specifically by engineering stem cells has been introduced to society. One strategy involves human leukocyte antigen (HLA) deletion through gene editing, affording allografts the capability to evade the host immune system. Another strategy involves immune cloak, which is the focus of this review, with emphasis on the overexpression of immune checkpoints and the blocking of immune cytotoxic pathways. Nevertheless, co-transplantation with mesenchymal stem cells (MSCs) and enhanced MSCs confers immune privilege to engraftments. This review summarizes recent studies on the intricacies of immune tolerance induction by engineering stem cells. In addition, we endeavor to deliberate upon the safety and limitations associated with this promising and potential therapeutic modality.
人类多能干细胞(hPSCs)在再生医学领域极具潜力。然而,免疫排斥仍然是干细胞治疗的主要障碍之一。尽管临床上有传统的免疫抑制剂,但副作用阻碍了hPSCs衍生物的广泛应用,影响了生存率和生活质量。近年来,社会上引入了多种旨在通过改造干细胞特异性诱导免疫耐受的策略。一种策略是通过基因编辑删除人类白细胞抗原(HLA),使同种异体移植物具备逃避宿主免疫系统的能力。另一种策略是免疫伪装,这也是本综述的重点,重点在于免疫检查点的过表达和免疫细胞毒性途径的阻断。此外,与间充质干细胞(MSCs)共移植以及增强的MSCs赋予移植物免疫特权。本综述总结了近期关于通过改造干细胞诱导免疫耐受复杂性的研究。此外,我们还努力探讨与这种有前景的潜在治疗方式相关的安全性和局限性。