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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...

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Autores principales: Hahn, Susanne A., Bellinghausen, Iris, Trinschek, Bettina, Becker, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
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.
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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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