Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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
_version_ 1783664162047524864
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
work_keys_str_mv AT izotovanatalia longtermlymphoidprogenitorsindependentlysustainnaivetandnkcellproductioninhumans
AT rivatchristine longtermlymphoidprogenitorsindependentlysustainnaivetandnkcellproductioninhumans
AT baricordicristina longtermlymphoidprogenitorsindependentlysustainnaivetandnkcellproductioninhumans
AT blancoelena longtermlymphoidprogenitorsindependentlysustainnaivetandnkcellproductioninhumans
AT pellindanilo longtermlymphoidprogenitorsindependentlysustainnaivetandnkcellproductioninhumans
AT watteleanor longtermlymphoidprogenitorsindependentlysustainnaivetandnkcellproductioninhumans
AT gkaziathinas longtermlymphoidprogenitorsindependentlysustainnaivetandnkcellproductioninhumans
AT adamsstuart longtermlymphoidprogenitorsindependentlysustainnaivetandnkcellproductioninhumans
AT gilmourkimberly longtermlymphoidprogenitorsindependentlysustainnaivetandnkcellproductioninhumans
AT bayfordjinhua longtermlymphoidprogenitorsindependentlysustainnaivetandnkcellproductioninhumans
AT boothclaire longtermlymphoidprogenitorsindependentlysustainnaivetandnkcellproductioninhumans
AT gasparhbobby longtermlymphoidprogenitorsindependentlysustainnaivetandnkcellproductioninhumans
AT thrasheradrianj longtermlymphoidprogenitorsindependentlysustainnaivetandnkcellproductioninhumans
AT biascoluca longtermlymphoidprogenitorsindependentlysustainnaivetandnkcellproductioninhumans