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Updates on Immune Therapies in Type 1 Diabetes

Multiple clinical trials investigating the efficacy and safety of immunotherapeutic interventions in new onset type 1 diabetes (T1D) have failed to yield long term clinical benefit. Lack of efficacy has frequently been attributed to an incomplete understanding of the pathways involved in T1D and the...

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Autores principales: Nambam, Bimota, Haller, Michael J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Touch Medical Media 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5813448/
https://www.ncbi.nlm.nih.gov/pubmed/29632594
http://dx.doi.org/10.17925/EE.2016.12.02.89
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author Nambam, Bimota
Haller, Michael J
author_facet Nambam, Bimota
Haller, Michael J
author_sort Nambam, Bimota
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description Multiple clinical trials investigating the efficacy and safety of immunotherapeutic interventions in new onset type 1 diabetes (T1D) have failed to yield long term clinical benefit. Lack of efficacy has frequently been attributed to an incomplete understanding of the pathways involved in T1D and the use of single immunotherapeutic agents. Recent mechanistic studies have improved our knowledge of the complex etiopathogenesis of T1D. This in turn has provided the framework for new and ongoing clinical trials in new onset T1D patients and at-risk subjects. Focus has also shifted towards the potential benefits of synergistic combinatorial approaches, both in terms of efficacy and the potential for reduced side effects. These efforts seek to develop intervention strategies that will preserve β-cell function, and ultimately prevent and reverse clinical disease.
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spelling pubmed-58134482018-04-09 Updates on Immune Therapies in Type 1 Diabetes Nambam, Bimota Haller, Michael J Eur Endocrinol Review Multiple clinical trials investigating the efficacy and safety of immunotherapeutic interventions in new onset type 1 diabetes (T1D) have failed to yield long term clinical benefit. Lack of efficacy has frequently been attributed to an incomplete understanding of the pathways involved in T1D and the use of single immunotherapeutic agents. Recent mechanistic studies have improved our knowledge of the complex etiopathogenesis of T1D. This in turn has provided the framework for new and ongoing clinical trials in new onset T1D patients and at-risk subjects. Focus has also shifted towards the potential benefits of synergistic combinatorial approaches, both in terms of efficacy and the potential for reduced side effects. These efforts seek to develop intervention strategies that will preserve β-cell function, and ultimately prevent and reverse clinical disease. Touch Medical Media 2016-08 2016-08-28 /pmc/articles/PMC5813448/ /pubmed/29632594 http://dx.doi.org/10.17925/EE.2016.12.02.89 Text en © Touch Medical Media 2016 http://creativecommons.org/licenses/by-nc/3.0/ Open Access: This article is published under the Creative Commons Attribution Noncommercial License, which permits any non-commercial use, distribution, adaptation and reproduction provided the original author(s) and source are given appropriate credit. © The Author(s) 2016
spellingShingle Review
Nambam, Bimota
Haller, Michael J
Updates on Immune Therapies in Type 1 Diabetes
title Updates on Immune Therapies in Type 1 Diabetes
title_full Updates on Immune Therapies in Type 1 Diabetes
title_fullStr Updates on Immune Therapies in Type 1 Diabetes
title_full_unstemmed Updates on Immune Therapies in Type 1 Diabetes
title_short Updates on Immune Therapies in Type 1 Diabetes
title_sort updates on immune therapies in type 1 diabetes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5813448/
https://www.ncbi.nlm.nih.gov/pubmed/29632594
http://dx.doi.org/10.17925/EE.2016.12.02.89
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