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Murine Models of Systemic Lupus Erythematosus
Systemic lupus erythematosus (SLE) is a multifactorial autoimmune disorder. The study of diverse mouse models of lupus has provided clues to the etiology of SLE. Spontaneous mouse models of lupus have led to identification of numerous susceptibility loci from which several candidate genes have emerg...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042628/ https://www.ncbi.nlm.nih.gov/pubmed/21403825 http://dx.doi.org/10.1155/2011/271694 |
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author | Perry, Daniel Sang, Allison Yin, Yiming Zheng, Ying-Yi Morel, Laurence |
author_facet | Perry, Daniel Sang, Allison Yin, Yiming Zheng, Ying-Yi Morel, Laurence |
author_sort | Perry, Daniel |
collection | PubMed |
description | Systemic lupus erythematosus (SLE) is a multifactorial autoimmune disorder. The study of diverse mouse models of lupus has provided clues to the etiology of SLE. Spontaneous mouse models of lupus have led to identification of numerous susceptibility loci from which several candidate genes have emerged. Meanwhile, induced models of lupus have provided insight into the role of environmental factors in lupus pathogenesis as well as provided a better understanding of cellular mechanisms involved in the onset and progression of disease. The SLE-like phenotypes present in these models have also served to screen numerous potential SLE therapies. Due to the complex nature of SLE, it is necessary to understand the effect specific targeted therapies have on immune homeostasis. Furthermore, knowledge gained from mouse models will provide novel therapy targets for the treatment of SLE. |
format | Text |
id | pubmed-3042628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-30426282011-03-14 Murine Models of Systemic Lupus Erythematosus Perry, Daniel Sang, Allison Yin, Yiming Zheng, Ying-Yi Morel, Laurence J Biomed Biotechnol Review Article Systemic lupus erythematosus (SLE) is a multifactorial autoimmune disorder. The study of diverse mouse models of lupus has provided clues to the etiology of SLE. Spontaneous mouse models of lupus have led to identification of numerous susceptibility loci from which several candidate genes have emerged. Meanwhile, induced models of lupus have provided insight into the role of environmental factors in lupus pathogenesis as well as provided a better understanding of cellular mechanisms involved in the onset and progression of disease. The SLE-like phenotypes present in these models have also served to screen numerous potential SLE therapies. Due to the complex nature of SLE, it is necessary to understand the effect specific targeted therapies have on immune homeostasis. Furthermore, knowledge gained from mouse models will provide novel therapy targets for the treatment of SLE. Hindawi Publishing Corporation 2011 2011-02-14 /pmc/articles/PMC3042628/ /pubmed/21403825 http://dx.doi.org/10.1155/2011/271694 Text en Copyright © 2011 Daniel Perry 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 Perry, Daniel Sang, Allison Yin, Yiming Zheng, Ying-Yi Morel, Laurence Murine Models of Systemic Lupus Erythematosus |
title | Murine Models of Systemic Lupus Erythematosus |
title_full | Murine Models of Systemic Lupus Erythematosus |
title_fullStr | Murine Models of Systemic Lupus Erythematosus |
title_full_unstemmed | Murine Models of Systemic Lupus Erythematosus |
title_short | Murine Models of Systemic Lupus Erythematosus |
title_sort | murine models of systemic lupus erythematosus |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042628/ https://www.ncbi.nlm.nih.gov/pubmed/21403825 http://dx.doi.org/10.1155/2011/271694 |
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