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A Three-dimensional Thymic Culture System to Generate Murine Induced Pluripotent Stem Cell-derived Tumor Antigen-specific Thymic Emigrants. | LitMetric

AI Article Synopsis

  • iPSC-derived T cells, enhanced through pre-rearranged T cell receptors and epigenetic rejuvenation, show potential for improving adoptive T cell therapy due to their unique properties.
  • Traditional methods for regenerating T cells from iPSCs lead to cells that do not resemble naïve T cells, limiting their therapeutic effectiveness.
  • A new three-dimensional thymic culture system successfully generates a homogeneous group of CD8αβ T cells that resemble naïve T cells, retaining critical functions such as proliferation and tumor suppression, and allowing for better understanding of T cell maturation.

Article Abstract

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191389PMC
http://dx.doi.org/10.3791/58672DOI Listing

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