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Islet cells in human type 1 diabetes: from recent advances to novel therapies – a symposium-based roadmap for future research

There is a growing understanding that the early phases of type 1 diabetes (T1D) are characterised by a deleterious dialogue between the pancreatic beta cells and the immune system. This, combined with the urgent need to better translate this growing knowledge into novel therapies, provided the backg...

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Detalles Bibliográficos
Autores principales: Cantley, J, Eizirik, D L, Latres, E, Dayan, C M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502961/
https://www.ncbi.nlm.nih.gov/pubmed/37493471
http://dx.doi.org/10.1530/JOE-23-0082
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author Cantley, J
Eizirik, D L
Latres, E
Dayan, C M
author_facet Cantley, J
Eizirik, D L
Latres, E
Dayan, C M
author_sort Cantley, J
collection PubMed
description There is a growing understanding that the early phases of type 1 diabetes (T1D) are characterised by a deleterious dialogue between the pancreatic beta cells and the immune system. This, combined with the urgent need to better translate this growing knowledge into novel therapies, provided the background for the JDRF–DiabetesUK–INNODIA–nPOD symposium entitled ‘Islet cells in human T1D: from recent advances to novel therapies’, which took place in Stockholm, Sweden, in September 2022. We provide in this article an overview of the main themes addressed in the symposium, pointing to both promising conclusions and key unmet needs that remain to be addressed in order to achieve better approaches to prevent or reverse T1D.
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spelling pubmed-105029612023-09-16 Islet cells in human type 1 diabetes: from recent advances to novel therapies – a symposium-based roadmap for future research Cantley, J Eizirik, D L Latres, E Dayan, C M J Endocrinol Review There is a growing understanding that the early phases of type 1 diabetes (T1D) are characterised by a deleterious dialogue between the pancreatic beta cells and the immune system. This, combined with the urgent need to better translate this growing knowledge into novel therapies, provided the background for the JDRF–DiabetesUK–INNODIA–nPOD symposium entitled ‘Islet cells in human T1D: from recent advances to novel therapies’, which took place in Stockholm, Sweden, in September 2022. We provide in this article an overview of the main themes addressed in the symposium, pointing to both promising conclusions and key unmet needs that remain to be addressed in order to achieve better approaches to prevent or reverse T1D. Bioscientifica Ltd 2023-08-31 /pmc/articles/PMC10502961/ /pubmed/37493471 http://dx.doi.org/10.1530/JOE-23-0082 Text en © the author(s) https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License. (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Review
Cantley, J
Eizirik, D L
Latres, E
Dayan, C M
Islet cells in human type 1 diabetes: from recent advances to novel therapies – a symposium-based roadmap for future research
title Islet cells in human type 1 diabetes: from recent advances to novel therapies – a symposium-based roadmap for future research
title_full Islet cells in human type 1 diabetes: from recent advances to novel therapies – a symposium-based roadmap for future research
title_fullStr Islet cells in human type 1 diabetes: from recent advances to novel therapies – a symposium-based roadmap for future research
title_full_unstemmed Islet cells in human type 1 diabetes: from recent advances to novel therapies – a symposium-based roadmap for future research
title_short Islet cells in human type 1 diabetes: from recent advances to novel therapies – a symposium-based roadmap for future research
title_sort islet cells in human type 1 diabetes: from recent advances to novel therapies – a symposium-based roadmap for future research
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502961/
https://www.ncbi.nlm.nih.gov/pubmed/37493471
http://dx.doi.org/10.1530/JOE-23-0082
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