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Generation of mature T cells from human hematopoietic stem/progenitor cells in artificial thymic organoids
Studies of human T cell development require robust model systems that recapitulate the full span of thymopoiesis, from hematopoietic stem and progenitor cells (HSPCs) through to mature T cells. Existing in vitro models induce T cell commitment from human HSPCs; however, differentiation into mature C...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5426913/ https://www.ncbi.nlm.nih.gov/pubmed/28369043 http://dx.doi.org/10.1038/nmeth.4237 |
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author | Seet, Christopher S. He, Chongbin Bethune, Michael T. Li, Suwen Chick, Brent Gschweng, Eric H. Zhu, Yuhua Kim, Kenneth Kohn, Donald B. Baltimore, David Crooks, Gay M. Montel-Hagen, Amélie |
author_facet | Seet, Christopher S. He, Chongbin Bethune, Michael T. Li, Suwen Chick, Brent Gschweng, Eric H. Zhu, Yuhua Kim, Kenneth Kohn, Donald B. Baltimore, David Crooks, Gay M. Montel-Hagen, Amélie |
author_sort | Seet, Christopher S. |
collection | PubMed |
description | Studies of human T cell development require robust model systems that recapitulate the full span of thymopoiesis, from hematopoietic stem and progenitor cells (HSPCs) through to mature T cells. Existing in vitro models induce T cell commitment from human HSPCs; however, differentiation into mature CD3+TCRab+ single positive (SP) CD8+ or CD4+ cells is limited. We describe here a serum-free, artificial thymic organoid (ATO) system that supports highly efficient and reproducible in vitro differentiation and positive selection of conventional human T cells from all sources of HSPCs. ATO-derived T cells exhibited mature naïve phenotypes, a diverse TCR repertoire, and TCR-dependent function. ATOs initiated with TCR-engineered HSPCs produced T cells with antigen specific cytotoxicity and near complete lack of endogenous TCR Vβ expression, consistent with allelic exclusion of Vβ loci. ATOs provide a robust tool for studying human T cell development and stem cell based approaches to engineered T cell therapies. |
format | Online Article Text |
id | pubmed-5426913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-54269132017-10-03 Generation of mature T cells from human hematopoietic stem/progenitor cells in artificial thymic organoids Seet, Christopher S. He, Chongbin Bethune, Michael T. Li, Suwen Chick, Brent Gschweng, Eric H. Zhu, Yuhua Kim, Kenneth Kohn, Donald B. Baltimore, David Crooks, Gay M. Montel-Hagen, Amélie Nat Methods Article Studies of human T cell development require robust model systems that recapitulate the full span of thymopoiesis, from hematopoietic stem and progenitor cells (HSPCs) through to mature T cells. Existing in vitro models induce T cell commitment from human HSPCs; however, differentiation into mature CD3+TCRab+ single positive (SP) CD8+ or CD4+ cells is limited. We describe here a serum-free, artificial thymic organoid (ATO) system that supports highly efficient and reproducible in vitro differentiation and positive selection of conventional human T cells from all sources of HSPCs. ATO-derived T cells exhibited mature naïve phenotypes, a diverse TCR repertoire, and TCR-dependent function. ATOs initiated with TCR-engineered HSPCs produced T cells with antigen specific cytotoxicity and near complete lack of endogenous TCR Vβ expression, consistent with allelic exclusion of Vβ loci. ATOs provide a robust tool for studying human T cell development and stem cell based approaches to engineered T cell therapies. 2017-04-03 2017-05 /pmc/articles/PMC5426913/ /pubmed/28369043 http://dx.doi.org/10.1038/nmeth.4237 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Seet, Christopher S. He, Chongbin Bethune, Michael T. Li, Suwen Chick, Brent Gschweng, Eric H. Zhu, Yuhua Kim, Kenneth Kohn, Donald B. Baltimore, David Crooks, Gay M. Montel-Hagen, Amélie Generation of mature T cells from human hematopoietic stem/progenitor cells in artificial thymic organoids |
title | Generation of mature T cells from human hematopoietic stem/progenitor cells in artificial thymic organoids |
title_full | Generation of mature T cells from human hematopoietic stem/progenitor cells in artificial thymic organoids |
title_fullStr | Generation of mature T cells from human hematopoietic stem/progenitor cells in artificial thymic organoids |
title_full_unstemmed | Generation of mature T cells from human hematopoietic stem/progenitor cells in artificial thymic organoids |
title_short | Generation of mature T cells from human hematopoietic stem/progenitor cells in artificial thymic organoids |
title_sort | generation of mature t cells from human hematopoietic stem/progenitor cells in artificial thymic organoids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5426913/ https://www.ncbi.nlm.nih.gov/pubmed/28369043 http://dx.doi.org/10.1038/nmeth.4237 |
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