重编程
诱导多能干细胞
生物
细胞生物学
免疫系统
细胞分化
先天免疫系统
干细胞
免疫学
细胞
胚胎干细胞
遗传学
基因
出处
期刊:Methods in molecular biology
日期:2019-12-03
卷期号:: 237-257
被引量:3
标识
DOI:10.1007/978-1-0716-0207-2_16
摘要
Reprogramming differentiated cells into induced pluripotent stem cells (iPSCs) consists in dedifferentiation of the cells into the pluripotent state, i.e., stem cells. Since T cells play a pivotal role in our immune system, T cell reprogramming into iPSCs and subsequent redifferentiation of iPSCs toward the original cells hold a great promise for future cell therapy and for further exploring the biology of such T cells. Mucosal-associated invariant T (MAIT) cells are an innate-like T cells linking innate immunity to adaptive immunity, and believed to be implicated in host protection to infection, in inflammation, and in immune homeostasis, which makes them an attractive target for the clinical intervention. In this chapter, we will outline the protocol for reprogramming MAIT cells to pluripotency with Sendai virus vector and redifferentiation. This technique will allow expansion of MAIT cells for cell therapy against the intractable infectious diseases such as HIV/Tuberculosis or cancer.
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