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Current Concepts: Mouse Models of Sjögren's Syndrome

Sjögren's syndrome (SjS) is a complex chronic autoimmune disease of unknown etiology which primarily targets the exocrine glands, resulting in eventual loss of secretory function. The disease can present as either primary SjS or secondary SjS, the latter of which occurs concomitantly with anoth...

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Detalles Bibliográficos
Autores principales: Lavoie, Tegan N., Lee, Byung Ha, Nguyen, Cuong Q.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018660/
https://www.ncbi.nlm.nih.gov/pubmed/21253584
http://dx.doi.org/10.1155/2011/549107
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author Lavoie, Tegan N.
Lee, Byung Ha
Nguyen, Cuong Q.
author_facet Lavoie, Tegan N.
Lee, Byung Ha
Nguyen, Cuong Q.
author_sort Lavoie, Tegan N.
collection PubMed
description Sjögren's syndrome (SjS) is a complex chronic autoimmune disease of unknown etiology which primarily targets the exocrine glands, resulting in eventual loss of secretory function. The disease can present as either primary SjS or secondary SjS, the latter of which occurs concomitantly with another autoimmune disease such as rheumatoid arthritis, systemic lupus erythematosus, scleroderma, or primary biliary cirrhosis. Current advancements in therapeutic prevention and treatment for SjS are impeded by lack of understanding in the pathophysiological and clinical progression of the disease. Development of appropriate mouse models for both primary and secondary SjS is needed in order to advance knowledge of this disease. This paper details important features, advantages, and pitfalls of current animal models of SjS, including spontaneous, transgenic, knockout, immunization, and transplantation chimera mouse models, and emphasizes the need for a better model in representing the human SjS phenotype.
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spelling pubmed-30186602011-01-20 Current Concepts: Mouse Models of Sjögren's Syndrome Lavoie, Tegan N. Lee, Byung Ha Nguyen, Cuong Q. J Biomed Biotechnol Review Article Sjögren's syndrome (SjS) is a complex chronic autoimmune disease of unknown etiology which primarily targets the exocrine glands, resulting in eventual loss of secretory function. The disease can present as either primary SjS or secondary SjS, the latter of which occurs concomitantly with another autoimmune disease such as rheumatoid arthritis, systemic lupus erythematosus, scleroderma, or primary biliary cirrhosis. Current advancements in therapeutic prevention and treatment for SjS are impeded by lack of understanding in the pathophysiological and clinical progression of the disease. Development of appropriate mouse models for both primary and secondary SjS is needed in order to advance knowledge of this disease. This paper details important features, advantages, and pitfalls of current animal models of SjS, including spontaneous, transgenic, knockout, immunization, and transplantation chimera mouse models, and emphasizes the need for a better model in representing the human SjS phenotype. Hindawi Publishing Corporation 2011 2010-12-30 /pmc/articles/PMC3018660/ /pubmed/21253584 http://dx.doi.org/10.1155/2011/549107 Text en Copyright © 2011 Tegan N. Lavoie et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Lavoie, Tegan N.
Lee, Byung Ha
Nguyen, Cuong Q.
Current Concepts: Mouse Models of Sjögren's Syndrome
title Current Concepts: Mouse Models of Sjögren's Syndrome
title_full Current Concepts: Mouse Models of Sjögren's Syndrome
title_fullStr Current Concepts: Mouse Models of Sjögren's Syndrome
title_full_unstemmed Current Concepts: Mouse Models of Sjögren's Syndrome
title_short Current Concepts: Mouse Models of Sjögren's Syndrome
title_sort current concepts: mouse models of sjögren's syndrome
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018660/
https://www.ncbi.nlm.nih.gov/pubmed/21253584
http://dx.doi.org/10.1155/2011/549107
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