Unknown

Dataset Information

0

Generation of Tumor Antigen-Specific iPSC-Derived Thymic Emigrants Using a 3D Thymic Culture System.


ABSTRACT: Induced pluripotent stem cell (iPSC)-derived T cells may provide future therapies for cancer patients, but those generated by current methods, such as the OP9/DLL1 system, have shown abnormalities that pose major barriers for clinical translation. Our data indicate that these iPSC-derived CD8 single-positive T cells are more like CD4+CD8+ double-positive T cells than mature naive T cells because they display phenotypic markers of developmental arrest and an innate-like phenotype after stimulation. We developed a 3D thymic culture system to avoid these aberrant developmental fates, generating a homogeneous subset of CD8??+ antigen-specific T cells, designated iPSC-derived thymic emigrants (iTEs). iTEs exhibit phenotypic and functional similarities to naive T cells both in vitro and in vivo, including the capacity for expansion, memory formation, and tumor suppression. These data illustrate the limitations of current methods and provide a tool to develop the next generation of iPSC-based antigen-specific immunotherapies.

SUBMITTER: Vizcardo R 

PROVIDER: S-EPMC5930030 | biostudies-literature | 2018 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications


Induced pluripotent stem cell (iPSC)-derived T cells may provide future therapies for cancer patients, but those generated by current methods, such as the OP9/DLL1 system, have shown abnormalities that pose major barriers for clinical translation. Our data indicate that these iPSC-derived CD8 single-positive T cells are more like CD4<sup>+</sup>CD8<sup>+</sup> double-positive T cells than mature naive T cells because they display phenotypic markers of developmental arrest and an innate-like phen  ...[more]

Similar Datasets

2018-02-28 | GSE105110 | GEO
| PRJNA414659 | ENA
| S-EPMC7289419 | biostudies-literature
| S-EPMC4332405 | biostudies-literature
2022-10-18 | GSE209997 | GEO
| S-EPMC5545745 | biostudies-literature
| S-EPMC3584139 | biostudies-literature