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Translating Treg Therapy in Humanized Mice
Regulatory T cells (Treg) control immune cell function as well as non-immunological processes. Their far-reaching regulatory activities suggest their functional manipulation as a means to sustainably and causally intervene with the course of diseases. Preclinical tools and strategies are however nee...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677486/ https://www.ncbi.nlm.nih.gov/pubmed/26697017 http://dx.doi.org/10.3389/fimmu.2015.00623 |
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author | Hahn, Susanne A. Bellinghausen, Iris Trinschek, Bettina Becker, Christian |
author_facet | Hahn, Susanne A. Bellinghausen, Iris Trinschek, Bettina Becker, Christian |
author_sort | Hahn, Susanne A. |
collection | PubMed |
description | Regulatory T cells (Treg) control immune cell function as well as non-immunological processes. Their far-reaching regulatory activities suggest their functional manipulation as a means to sustainably and causally intervene with the course of diseases. Preclinical tools and strategies are however needed to further test and develop interventional strategies outside the human body. “Humanized” mouse models consisting of mice engrafted with human immune cells and tissues provide new tools to analyze human Treg ontogeny, immunobiology, and therapy. Here, we summarize the current state of humanized mouse models as a means to study human Treg function at the molecular level and to design strategies to harness these cells for therapeutic purposes. |
format | Online Article Text |
id | pubmed-4677486 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-46774862015-12-22 Translating Treg Therapy in Humanized Mice Hahn, Susanne A. Bellinghausen, Iris Trinschek, Bettina Becker, Christian Front Immunol Immunology Regulatory T cells (Treg) control immune cell function as well as non-immunological processes. Their far-reaching regulatory activities suggest their functional manipulation as a means to sustainably and causally intervene with the course of diseases. Preclinical tools and strategies are however needed to further test and develop interventional strategies outside the human body. “Humanized” mouse models consisting of mice engrafted with human immune cells and tissues provide new tools to analyze human Treg ontogeny, immunobiology, and therapy. Here, we summarize the current state of humanized mouse models as a means to study human Treg function at the molecular level and to design strategies to harness these cells for therapeutic purposes. Frontiers Media S.A. 2015-12-14 /pmc/articles/PMC4677486/ /pubmed/26697017 http://dx.doi.org/10.3389/fimmu.2015.00623 Text en Copyright © 2015 Hahn, Bellinghausen, Trinschek and Becker. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Hahn, Susanne A. Bellinghausen, Iris Trinschek, Bettina Becker, Christian Translating Treg Therapy in Humanized Mice |
title | Translating Treg Therapy in Humanized Mice |
title_full | Translating Treg Therapy in Humanized Mice |
title_fullStr | Translating Treg Therapy in Humanized Mice |
title_full_unstemmed | Translating Treg Therapy in Humanized Mice |
title_short | Translating Treg Therapy in Humanized Mice |
title_sort | translating treg therapy in humanized mice |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677486/ https://www.ncbi.nlm.nih.gov/pubmed/26697017 http://dx.doi.org/10.3389/fimmu.2015.00623 |
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