Suppressive IL-17A+Foxp3+ and ex-Th17 IL-17AnegFoxp3+ Treg cells are a source of tumour-associated Treg cells

Th17 cells can transdifferentiate into regulatory T (Treg) cells. Here the authors characterize tumour-driven Th17-to-Tregcell transdifferentiation and identify potential cancer therapy targets.

Bibliographic Details
Main Authors: Stephanie Downs-Canner, Sara Berkey, Greg M. Delgoffe, Robert P. Edwards, Tyler Curiel, Kunle Odunsi, David L. Bartlett, Nataša Obermajer
Format: Article
Language:English
Published: Nature Portfolio 2017-03-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/ncomms14649
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author Stephanie Downs-Canner
Sara Berkey
Greg M. Delgoffe
Robert P. Edwards
Tyler Curiel
Kunle Odunsi
David L. Bartlett
Nataša Obermajer
author_facet Stephanie Downs-Canner
Sara Berkey
Greg M. Delgoffe
Robert P. Edwards
Tyler Curiel
Kunle Odunsi
David L. Bartlett
Nataša Obermajer
author_sort Stephanie Downs-Canner
collection DOAJ
description Th17 cells can transdifferentiate into regulatory T (Treg) cells. Here the authors characterize tumour-driven Th17-to-Tregcell transdifferentiation and identify potential cancer therapy targets.
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spelling doaj.art-9e8d4eb2095e4915964c459f3f8ece802022-12-21T20:28:48ZengNature PortfolioNature Communications2041-17232017-03-018111510.1038/ncomms14649Suppressive IL-17A+Foxp3+ and ex-Th17 IL-17AnegFoxp3+ Treg cells are a source of tumour-associated Treg cellsStephanie Downs-Canner0Sara Berkey1Greg M. Delgoffe2Robert P. Edwards3Tyler Curiel4Kunle Odunsi5David L. Bartlett6Nataša Obermajer7Department of Surgical Oncology, University of PittsburghDepartment of Surgical Oncology, University of PittsburghUniversity of Pittsburgh Cancer InstituteUniversity of Pittsburgh Cancer InstituteUT Health Science Center at San AntonioDepartments of Gynecologic Oncology and Immunology, Roswell Park Cancer InstituteDepartment of Surgical Oncology, University of PittsburghDepartment of Surgical Oncology, University of PittsburghTh17 cells can transdifferentiate into regulatory T (Treg) cells. Here the authors characterize tumour-driven Th17-to-Tregcell transdifferentiation and identify potential cancer therapy targets.https://doi.org/10.1038/ncomms14649
spellingShingle Stephanie Downs-Canner
Sara Berkey
Greg M. Delgoffe
Robert P. Edwards
Tyler Curiel
Kunle Odunsi
David L. Bartlett
Nataša Obermajer
Suppressive IL-17A+Foxp3+ and ex-Th17 IL-17AnegFoxp3+ Treg cells are a source of tumour-associated Treg cells
Nature Communications
title Suppressive IL-17A+Foxp3+ and ex-Th17 IL-17AnegFoxp3+ Treg cells are a source of tumour-associated Treg cells
title_full Suppressive IL-17A+Foxp3+ and ex-Th17 IL-17AnegFoxp3+ Treg cells are a source of tumour-associated Treg cells
title_fullStr Suppressive IL-17A+Foxp3+ and ex-Th17 IL-17AnegFoxp3+ Treg cells are a source of tumour-associated Treg cells
title_full_unstemmed Suppressive IL-17A+Foxp3+ and ex-Th17 IL-17AnegFoxp3+ Treg cells are a source of tumour-associated Treg cells
title_short Suppressive IL-17A+Foxp3+ and ex-Th17 IL-17AnegFoxp3+ Treg cells are a source of tumour-associated Treg cells
title_sort suppressive il 17a foxp3 and ex th17 il 17anegfoxp3 treg cells are a source of tumour associated treg cells
url https://doi.org/10.1038/ncomms14649
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