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An Atlas of Human Regulatory T Helper-like Cells Reveals Features of Th2-like Tregs that Support a Tumorigenic Environment
Regulatory T cells (Tregs) play a pivotal role in maintaining immunological tolerance, but they can also play a detrimental role by preventing antitumor responses. Here, we characterized T helper (Th)-like Treg subsets to further delineate their biological function and tissue distribution, focusing...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529316/ https://www.ncbi.nlm.nih.gov/pubmed/28723576 http://dx.doi.org/10.1016/j.celrep.2017.06.079 |
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author | Halim, Leena Romano, Marco McGregor, Reuben Correa, Isabel Pavlidis, Polychronis Grageda, Nathali Hoong, Sec-Julie Yuksel, Muhammed Jassem, Wayel Hannen, Rosalind F. Ong, Mark Mckinney, Olivia Hayee, Bu’Hussain Karagiannis, Sophia N. Powell, Nicholas Lechler, Robert I. Nova-Lamperti, Estefania Lombardi, Giovanna |
author_facet | Halim, Leena Romano, Marco McGregor, Reuben Correa, Isabel Pavlidis, Polychronis Grageda, Nathali Hoong, Sec-Julie Yuksel, Muhammed Jassem, Wayel Hannen, Rosalind F. Ong, Mark Mckinney, Olivia Hayee, Bu’Hussain Karagiannis, Sophia N. Powell, Nicholas Lechler, Robert I. Nova-Lamperti, Estefania Lombardi, Giovanna |
author_sort | Halim, Leena |
collection | PubMed |
description | Regulatory T cells (Tregs) play a pivotal role in maintaining immunological tolerance, but they can also play a detrimental role by preventing antitumor responses. Here, we characterized T helper (Th)-like Treg subsets to further delineate their biological function and tissue distribution, focusing on their possible contribution to disease states. RNA sequencing and functional assays revealed that Th2-like Tregs displayed higher viability and autocrine interleukin-2 (IL-2)-mediated activation than other subsets. Th2-like Tregs were preferentially found in tissues rather than circulation and exhibited the highest migratory capacity toward chemokines enriched at tumor sites. These cellular responses led us to hypothesize that this subset could play a role in maintaining a tumorigenic environment. Concurrently, Th2-like Tregs were enriched specifically in malignant tissues from patients with melanoma and colorectal cancer compared to healthy tissue. Overall, our results suggest that Th2-like Tregs may contribute to a tumorigenic environment due to their increased cell survival, higher migratory capacity, and selective T-effector suppressive ability. |
format | Online Article Text |
id | pubmed-5529316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55293162017-08-08 An Atlas of Human Regulatory T Helper-like Cells Reveals Features of Th2-like Tregs that Support a Tumorigenic Environment Halim, Leena Romano, Marco McGregor, Reuben Correa, Isabel Pavlidis, Polychronis Grageda, Nathali Hoong, Sec-Julie Yuksel, Muhammed Jassem, Wayel Hannen, Rosalind F. Ong, Mark Mckinney, Olivia Hayee, Bu’Hussain Karagiannis, Sophia N. Powell, Nicholas Lechler, Robert I. Nova-Lamperti, Estefania Lombardi, Giovanna Cell Rep Resource Regulatory T cells (Tregs) play a pivotal role in maintaining immunological tolerance, but they can also play a detrimental role by preventing antitumor responses. Here, we characterized T helper (Th)-like Treg subsets to further delineate their biological function and tissue distribution, focusing on their possible contribution to disease states. RNA sequencing and functional assays revealed that Th2-like Tregs displayed higher viability and autocrine interleukin-2 (IL-2)-mediated activation than other subsets. Th2-like Tregs were preferentially found in tissues rather than circulation and exhibited the highest migratory capacity toward chemokines enriched at tumor sites. These cellular responses led us to hypothesize that this subset could play a role in maintaining a tumorigenic environment. Concurrently, Th2-like Tregs were enriched specifically in malignant tissues from patients with melanoma and colorectal cancer compared to healthy tissue. Overall, our results suggest that Th2-like Tregs may contribute to a tumorigenic environment due to their increased cell survival, higher migratory capacity, and selective T-effector suppressive ability. Cell Press 2017-07-18 /pmc/articles/PMC5529316/ /pubmed/28723576 http://dx.doi.org/10.1016/j.celrep.2017.06.079 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Resource Halim, Leena Romano, Marco McGregor, Reuben Correa, Isabel Pavlidis, Polychronis Grageda, Nathali Hoong, Sec-Julie Yuksel, Muhammed Jassem, Wayel Hannen, Rosalind F. Ong, Mark Mckinney, Olivia Hayee, Bu’Hussain Karagiannis, Sophia N. Powell, Nicholas Lechler, Robert I. Nova-Lamperti, Estefania Lombardi, Giovanna An Atlas of Human Regulatory T Helper-like Cells Reveals Features of Th2-like Tregs that Support a Tumorigenic Environment |
title | An Atlas of Human Regulatory T Helper-like Cells Reveals Features of Th2-like Tregs that Support a Tumorigenic Environment |
title_full | An Atlas of Human Regulatory T Helper-like Cells Reveals Features of Th2-like Tregs that Support a Tumorigenic Environment |
title_fullStr | An Atlas of Human Regulatory T Helper-like Cells Reveals Features of Th2-like Tregs that Support a Tumorigenic Environment |
title_full_unstemmed | An Atlas of Human Regulatory T Helper-like Cells Reveals Features of Th2-like Tregs that Support a Tumorigenic Environment |
title_short | An Atlas of Human Regulatory T Helper-like Cells Reveals Features of Th2-like Tregs that Support a Tumorigenic Environment |
title_sort | atlas of human regulatory t helper-like cells reveals features of th2-like tregs that support a tumorigenic environment |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529316/ https://www.ncbi.nlm.nih.gov/pubmed/28723576 http://dx.doi.org/10.1016/j.celrep.2017.06.079 |
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