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From IgG Fusion Proteins to Engineered-Specific Human Regulatory T Cells: A Life of Tolerance
Recent efforts have concentrated on approaches to expand and “specify” human regulatory T cells (Tregs) and to apply them to modulate adverse immune responses in autoimmunity and hemophilia. We have used retroviral transduction of specific T-cell receptor, single chain Fv, or antigen domains in Treg...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693857/ https://www.ncbi.nlm.nih.gov/pubmed/29181011 http://dx.doi.org/10.3389/fimmu.2017.01576 |
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author | Scott, David W. |
author_facet | Scott, David W. |
author_sort | Scott, David W. |
collection | PubMed |
description | Recent efforts have concentrated on approaches to expand and “specify” human regulatory T cells (Tregs) and to apply them to modulate adverse immune responses in autoimmunity and hemophilia. We have used retroviral transduction of specific T-cell receptor, single chain Fv, or antigen domains in Tregs to achieve this goal. Each of these approaches have advantages and disadvantages. Results with these engineered T cells and evolution of the research developments and paths that led to the development of specific regulatory approaches for tolerance are summarized. |
format | Online Article Text |
id | pubmed-5693857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56938572017-11-27 From IgG Fusion Proteins to Engineered-Specific Human Regulatory T Cells: A Life of Tolerance Scott, David W. Front Immunol Immunology Recent efforts have concentrated on approaches to expand and “specify” human regulatory T cells (Tregs) and to apply them to modulate adverse immune responses in autoimmunity and hemophilia. We have used retroviral transduction of specific T-cell receptor, single chain Fv, or antigen domains in Tregs to achieve this goal. Each of these approaches have advantages and disadvantages. Results with these engineered T cells and evolution of the research developments and paths that led to the development of specific regulatory approaches for tolerance are summarized. Frontiers Media S.A. 2017-11-13 /pmc/articles/PMC5693857/ /pubmed/29181011 http://dx.doi.org/10.3389/fimmu.2017.01576 Text en Copyright © 2017 Scott. 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 Scott, David W. From IgG Fusion Proteins to Engineered-Specific Human Regulatory T Cells: A Life of Tolerance |
title | From IgG Fusion Proteins to Engineered-Specific Human Regulatory T Cells: A Life of Tolerance |
title_full | From IgG Fusion Proteins to Engineered-Specific Human Regulatory T Cells: A Life of Tolerance |
title_fullStr | From IgG Fusion Proteins to Engineered-Specific Human Regulatory T Cells: A Life of Tolerance |
title_full_unstemmed | From IgG Fusion Proteins to Engineered-Specific Human Regulatory T Cells: A Life of Tolerance |
title_short | From IgG Fusion Proteins to Engineered-Specific Human Regulatory T Cells: A Life of Tolerance |
title_sort | from igg fusion proteins to engineered-specific human regulatory t cells: a life of tolerance |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693857/ https://www.ncbi.nlm.nih.gov/pubmed/29181011 http://dx.doi.org/10.3389/fimmu.2017.01576 |
work_keys_str_mv | AT scottdavidw fromiggfusionproteinstoengineeredspecifichumanregulatorytcellsalifeoftolerance |