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Immunotherapy of type 1 diabetes: lessons for other autoimmune diseases

CHAPTER SUMMARY: The nonobese diabetic (NOD) mouse is a well-recognised animal model of spontaneous autoimmune insulin-dependent diabetes mellitus. The disease is T-cell mediated, involving both CD4 and CD8 cells. Its progress is controlled by a variety of regulatory T cells. An unprecedented number...

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Autor principal: Bach, Jean-François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3240130/
https://www.ncbi.nlm.nih.gov/pubmed/12110118
http://dx.doi.org/10.1186/ar554
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author Bach, Jean-François
author_facet Bach, Jean-François
author_sort Bach, Jean-François
collection PubMed
description CHAPTER SUMMARY: The nonobese diabetic (NOD) mouse is a well-recognised animal model of spontaneous autoimmune insulin-dependent diabetes mellitus. The disease is T-cell mediated, involving both CD4 and CD8 cells. Its progress is controlled by a variety of regulatory T cells. An unprecedented number of immunological treatments have been assessed in this mouse strain. This chapter systematically reviews most of these therapeutic manoeuvres, discussing them in the context of their significance with regard to the underlying mechanisms and the potential clinical applications. The contrast between the surprisingly high rate of success found for a multitude of treatments (more than 160) administered early in the natural history of the disease and the few treatments active at a late stage is discussed in depth. Most of the concepts and strategies derived from this model apply to other autoimmune diseases, for which no such diversified data are available.
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spelling pubmed-32401302011-12-16 Immunotherapy of type 1 diabetes: lessons for other autoimmune diseases Bach, Jean-François Arthritis Res Review CHAPTER SUMMARY: The nonobese diabetic (NOD) mouse is a well-recognised animal model of spontaneous autoimmune insulin-dependent diabetes mellitus. The disease is T-cell mediated, involving both CD4 and CD8 cells. Its progress is controlled by a variety of regulatory T cells. An unprecedented number of immunological treatments have been assessed in this mouse strain. This chapter systematically reviews most of these therapeutic manoeuvres, discussing them in the context of their significance with regard to the underlying mechanisms and the potential clinical applications. The contrast between the surprisingly high rate of success found for a multitude of treatments (more than 160) administered early in the natural history of the disease and the few treatments active at a late stage is discussed in depth. Most of the concepts and strategies derived from this model apply to other autoimmune diseases, for which no such diversified data are available. BioMed Central 2002 2002-05-09 /pmc/articles/PMC3240130/ /pubmed/12110118 http://dx.doi.org/10.1186/ar554 Text en Copyright ©2002 BioMed Central Ltd
spellingShingle Review
Bach, Jean-François
Immunotherapy of type 1 diabetes: lessons for other autoimmune diseases
title Immunotherapy of type 1 diabetes: lessons for other autoimmune diseases
title_full Immunotherapy of type 1 diabetes: lessons for other autoimmune diseases
title_fullStr Immunotherapy of type 1 diabetes: lessons for other autoimmune diseases
title_full_unstemmed Immunotherapy of type 1 diabetes: lessons for other autoimmune diseases
title_short Immunotherapy of type 1 diabetes: lessons for other autoimmune diseases
title_sort immunotherapy of type 1 diabetes: lessons for other autoimmune diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3240130/
https://www.ncbi.nlm.nih.gov/pubmed/12110118
http://dx.doi.org/10.1186/ar554
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