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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...

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Autores principales: Kroger, Charles J., Clark, Matthew, Ke, Qi, Tisch, Roland M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
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.
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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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