A Three-dimensional Thymic Culture System to Generate Murine Induced Pluripotent Stem Cell-derived Tumor Antigen-specific Thymic Emigrants
Author(s) -
Raul Vizcardo,
S.M. Rafiqul Islam,
Takuya Maeda,
Naritaka Tamaoki,
Meghan L. Good,
Nicholas D. Klemen,
Marta BoschMarcé,
Li Jia,
Mikhael J. Kruhlak,
Nicholas P. Restifo
Publication year - 2019
Publication title -
journal of visualized experiments
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.596
H-Index - 91
ISSN - 1940-087X
DOI - 10.3791/58672
Subject(s) - induced pluripotent stem cell , biology , microbiology and biotechnology , t cell , cd8 , stem cell , adoptive cell transfer , antigen , cytotoxic t cell , cellular differentiation , immunology , cancer research , in vitro , embryonic stem cell , immune system , genetics , gene
The inheritance of pre-rearranged T cell receptors (TCRs) and their epigenetic rejuvenation make induced pluripotent stem cell (iPSC)-derived T cells a promising source for adoptive T cell therapy (ACT). However, classical in vitro methods for producing regenerated T cells from iPSC result in either innate-like or terminally differentiated T cells, which are phenotypically and functionally distinct from naïve T cells. Recently, a novel three-dimensional (3D) thymic culture system was developed to generate a homogenous subset of CD8αβ + antigen-specific T cells with a naïve T cell-like functional phenotype, including the capacity for proliferation, memory formation, and tumor suppression in vivo. This protocol avoids aberrant developmental fates, allowing for the generation of clinically relevant iPSC-derived T cells, designated as iPSC-derived thymic emigrants (iTE), while also providing a potent tool to elucidate the subsequent functions necessary for T cell maturation after thymic selection.
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