Genetic control of disease in an experimental model for Sjögren's syndrome
- PMID: 19216731
- PMCID: PMC2688230
- DOI: 10.1186/ar2583
Genetic control of disease in an experimental model for Sjögren's syndrome
Abstract
Sjögren's syndrome is an autoimmune disease with a complex etiology depending on hereditary and environmental factors. The disease is characterized by lymphocytic infiltration and inflammation in the salivary and lacrimal glands, leading to oral and ocular dryness. To understand the genetic susceptibility in Sjögren's syndrome, studies of disease phenotypes have been performed in the non-obese diabetic (NOD) mouse. By the identification of genetic regions controlling development of autoimmune exocrinopathy in the NOD mouse and by reducing one of these regions considerably, Nguyen et al. in a recent issue of Arthritis Research and Therapy propose candidate genes for development of Sjögren's syndrome.
Comment on
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Identification of possible candidate genes regulating Sjögren's syndrome-associated autoimmunity: a potential role for TNFSF4 in autoimmune exocrinopathy.Arthritis Res Ther. 2008;10(6):R137. doi: 10.1186/ar2560. Epub 2008 Nov 25. Arthritis Res Ther. 2008. PMID: 19032782 Free PMC article.
References
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- Johannesson M, Karlsson J, Wernhoff P, Nandakumar KS, Lindqvist AK, Olsson L, Cook AD, Andersson Å, Holmdahl R. Identification of epistasis through a partial advanced intercross reveals three arthritis loci within the Cia5 QTL in mice. Genes Immun. 2005;6:175–185. doi: 10.1038/sj.gene.6364155. - DOI - PubMed
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