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Long-term lymphoid progenitors independently sustain naïve T and NK cell production in humans
Our mathematical model of integration site data in clinical gene therapy supported the existence of long-term lymphoid progenitors capable of surviving independently from hematopoietic stem cells. To date, no experimental setting has been available to validate this prediction. We here report evidenc...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954865/ https://www.ncbi.nlm.nih.gov/pubmed/33712608 http://dx.doi.org/10.1038/s41467-021-21834-9 |
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author | Izotova, Natalia Rivat, Christine Baricordi, Cristina Blanco, Elena Pellin, Danilo Watt, Eleanor Gkazi, Athina S. Adams, Stuart Gilmour, Kimberly Bayford, Jinhua Booth, Claire Gaspar, H. Bobby Thrasher, Adrian J. Biasco, Luca |
author_facet | Izotova, Natalia Rivat, Christine Baricordi, Cristina Blanco, Elena Pellin, Danilo Watt, Eleanor Gkazi, Athina S. Adams, Stuart Gilmour, Kimberly Bayford, Jinhua Booth, Claire Gaspar, H. Bobby Thrasher, Adrian J. Biasco, Luca |
author_sort | Izotova, Natalia |
collection | PubMed |
description | Our mathematical model of integration site data in clinical gene therapy supported the existence of long-term lymphoid progenitors capable of surviving independently from hematopoietic stem cells. To date, no experimental setting has been available to validate this prediction. We here report evidence of a population of lymphoid progenitors capable of independently maintaining T and NK cell production for 15 years in humans. The gene therapy patients of this study lack vector-positive myeloid/B cells indicating absence of engineered stem cells but retain gene marking in both T and NK. Decades after treatment, we can still detect and analyse transduced naïve T cells whose production is likely maintained by a population of long-term lymphoid progenitors. By tracking insertional clonal markers overtime, we suggest that these progenitors can support both T and NK cell production. Identification of these long-term lymphoid progenitors could be utilised for the development of next generation gene- and cancer-immunotherapies. |
format | Online Article Text |
id | pubmed-7954865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79548652021-03-28 Long-term lymphoid progenitors independently sustain naïve T and NK cell production in humans Izotova, Natalia Rivat, Christine Baricordi, Cristina Blanco, Elena Pellin, Danilo Watt, Eleanor Gkazi, Athina S. Adams, Stuart Gilmour, Kimberly Bayford, Jinhua Booth, Claire Gaspar, H. Bobby Thrasher, Adrian J. Biasco, Luca Nat Commun Article Our mathematical model of integration site data in clinical gene therapy supported the existence of long-term lymphoid progenitors capable of surviving independently from hematopoietic stem cells. To date, no experimental setting has been available to validate this prediction. We here report evidence of a population of lymphoid progenitors capable of independently maintaining T and NK cell production for 15 years in humans. The gene therapy patients of this study lack vector-positive myeloid/B cells indicating absence of engineered stem cells but retain gene marking in both T and NK. Decades after treatment, we can still detect and analyse transduced naïve T cells whose production is likely maintained by a population of long-term lymphoid progenitors. By tracking insertional clonal markers overtime, we suggest that these progenitors can support both T and NK cell production. Identification of these long-term lymphoid progenitors could be utilised for the development of next generation gene- and cancer-immunotherapies. Nature Publishing Group UK 2021-03-12 /pmc/articles/PMC7954865/ /pubmed/33712608 http://dx.doi.org/10.1038/s41467-021-21834-9 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Izotova, Natalia Rivat, Christine Baricordi, Cristina Blanco, Elena Pellin, Danilo Watt, Eleanor Gkazi, Athina S. Adams, Stuart Gilmour, Kimberly Bayford, Jinhua Booth, Claire Gaspar, H. Bobby Thrasher, Adrian J. Biasco, Luca Long-term lymphoid progenitors independently sustain naïve T and NK cell production in humans |
title | Long-term lymphoid progenitors independently sustain naïve T and NK cell production in humans |
title_full | Long-term lymphoid progenitors independently sustain naïve T and NK cell production in humans |
title_fullStr | Long-term lymphoid progenitors independently sustain naïve T and NK cell production in humans |
title_full_unstemmed | Long-term lymphoid progenitors independently sustain naïve T and NK cell production in humans |
title_short | Long-term lymphoid progenitors independently sustain naïve T and NK cell production in humans |
title_sort | long-term lymphoid progenitors independently sustain naïve t and nk cell production in humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954865/ https://www.ncbi.nlm.nih.gov/pubmed/33712608 http://dx.doi.org/10.1038/s41467-021-21834-9 |
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