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基因工程改造低免疫原性通用多能干细胞的策略

Strategies for Genetically Engineering Hypoimmunogenic Universal Pluripotent Stem Cells.

作者信息

Zhao Wei, Lei Anhua, Tian Lin, Wang Xudong, Correia Cristina, Weiskittel Taylor, Li Hu, Trounson Alan, Fu Qiuli, Yao Ke, Zhang Jin

机构信息

Bone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310058, China; Zhejiang Provincial Key Lab of Ophthalmology, Eye Center of the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310058, China; Institute of Hematology, Zhejiang University, Hangzhou 310058, China.

Bone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310058, China; Institute of Hematology, Zhejiang University, Hangzhou 310058, China.

出版信息

iScience. 2020 Jun 26;23(6):101162. doi: 10.1016/j.isci.2020.101162. Epub 2020 May 17.

Abstract

Despite progress in developing cell therapies, such as T cell or stem cell therapies to treat diseases, immunoincompatibility remains a major barrier to clinical application. Given the fact that a host's immune system may reject allogeneic transplanted cells, methods have been developed to genetically modify patients' primary cells. To advance beyond this time-consuming and costly approach, recent research efforts focus on generating universal pluripotent stem cells to benefit a broader spectrum of patients. In this review, we first summarize current achievements to harness immunosuppressive mechanisms in cells to reduce immunogenicity. Then, we discuss several recent studies demonstrating the feasibility of genetically modifying pluripotent stem cells to escape immune attack and summarize the methods to evaluate hypoimmunogenicity. Although challenges remain, progress to develop genetically engineered universal pluripotent stem cells holds the promise of expediting their use in future gene and cell therapeutics and regenerative medicine.

摘要

尽管在开发细胞疗法(如用于治疗疾病的T细胞或干细胞疗法)方面取得了进展,但免疫不相容性仍然是临床应用的主要障碍。鉴于宿主的免疫系统可能会排斥同种异体移植细胞,人们已经开发出对患者原代细胞进行基因改造的方法。为了超越这种耗时且昂贵的方法,最近的研究工作集中在生成通用多能干细胞,以使更广泛的患者受益。在这篇综述中,我们首先总结了当前利用细胞免疫抑制机制降低免疫原性的成果。然后,我们讨论了最近的几项研究,这些研究证明了对多能干细胞进行基因改造以逃避免疫攻击的可行性,并总结了评估低免疫原性的方法。尽管挑战依然存在,但开发基因工程通用多能干细胞的进展有望加快其在未来基因和细胞治疗以及再生医学中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08d4/7270609/7c47ff7bbd8a/gr1.jpg

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