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Therapies to Suppress β Cell Autoimmunity in Type 1 Diabetes
Type 1 diabetes (T1D) is an autoimmune disease that is generally considered to be T cell-driven. Accordingly, most strategies of immunotherapy for T1D prevention and treatment in the clinic have targeted the T cell compartment. To date, however, immunotherapy has had only limited clinical success. A...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105696/ https://www.ncbi.nlm.nih.gov/pubmed/30166987 http://dx.doi.org/10.3389/fimmu.2018.01891 |
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author | Kroger, Charles J. Clark, Matthew Ke, Qi Tisch, Roland M. |
author_facet | Kroger, Charles J. Clark, Matthew Ke, Qi Tisch, Roland M. |
author_sort | Kroger, Charles J. |
collection | PubMed |
description | Type 1 diabetes (T1D) is an autoimmune disease that is generally considered to be T cell-driven. Accordingly, most strategies of immunotherapy for T1D prevention and treatment in the clinic have targeted the T cell compartment. To date, however, immunotherapy has had only limited clinical success. Although certain immunotherapies have promoted a protective effect, efficacy is often short-term and acquired immunity may be impacted. This has led to the consideration of combining different approaches with the goal of achieving a synergistic therapeutic response. In this review, we will discuss the status of various T1D therapeutic strategies tested in the clinic, as well as possible combinatorial approaches to restore β cell tolerance. |
format | Online Article Text |
id | pubmed-6105696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61056962018-08-30 Therapies to Suppress β Cell Autoimmunity in Type 1 Diabetes Kroger, Charles J. Clark, Matthew Ke, Qi Tisch, Roland M. Front Immunol Immunology Type 1 diabetes (T1D) is an autoimmune disease that is generally considered to be T cell-driven. Accordingly, most strategies of immunotherapy for T1D prevention and treatment in the clinic have targeted the T cell compartment. To date, however, immunotherapy has had only limited clinical success. Although certain immunotherapies have promoted a protective effect, efficacy is often short-term and acquired immunity may be impacted. This has led to the consideration of combining different approaches with the goal of achieving a synergistic therapeutic response. In this review, we will discuss the status of various T1D therapeutic strategies tested in the clinic, as well as possible combinatorial approaches to restore β cell tolerance. Frontiers Media S.A. 2018-08-16 /pmc/articles/PMC6105696/ /pubmed/30166987 http://dx.doi.org/10.3389/fimmu.2018.01891 Text en Copyright © 2018 Kroger, Clark, Ke and Tisch. https://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) and the copyright owner(s) 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 Kroger, Charles J. Clark, Matthew Ke, Qi Tisch, Roland M. Therapies to Suppress β Cell Autoimmunity in Type 1 Diabetes |
title | Therapies to Suppress β Cell Autoimmunity in Type 1 Diabetes |
title_full | Therapies to Suppress β Cell Autoimmunity in Type 1 Diabetes |
title_fullStr | Therapies to Suppress β Cell Autoimmunity in Type 1 Diabetes |
title_full_unstemmed | Therapies to Suppress β Cell Autoimmunity in Type 1 Diabetes |
title_short | Therapies to Suppress β Cell Autoimmunity in Type 1 Diabetes |
title_sort | therapies to suppress β cell autoimmunity in type 1 diabetes |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105696/ https://www.ncbi.nlm.nih.gov/pubmed/30166987 http://dx.doi.org/10.3389/fimmu.2018.01891 |
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