dc.contributor.author | Lavoie, Tegan N. | |
dc.contributor.author | Lee, Byung Ha | |
dc.contributor.author | Nguyen, Cuong Q. | |
dc.date.accessioned | 2011-03-03T18:24:28Z | |
dc.date.available | 2011-03-03T18:24:28Z | |
dc.date.issued | 2010-11 | |
dc.date.submitted | 2010-09 | |
dc.identifier.issn | 1110-7243 | |
dc.identifier.uri | http://hdl.handle.net/1721.1/61385 | |
dc.description.abstract | 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. | en_US |
dc.description.sponsorship | National Institutes of Health (U.S.) (PHS Grant K99DE018958) | en_US |
dc.description.sponsorship | National Institutes of Health (U.S.) (PHS Grant R21AI081952) | en_US |
dc.description.sponsorship | University of Florida. Center for Orphaned Autoimmune Disorders | en_US |
dc.description.sponsorship | Sjögren’s Syndrome Foundation | en_US |
dc.language.iso | en_US | |
dc.publisher | Hindawi Pub. Corp. | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1155/2011/549107 | en_US |
dc.rights | Creative Commons Attribution | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by/2.0/ | en_US |
dc.source | Hindawi | en_US |
dc.title | Current Concepts : Mouse Models of Sjögren’s Syndrome | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Tegan N. Lavoie, Byung Ha Lee, and Cuong Q. Nguyen, “Current Concepts: Mouse Models of Sjögren's Syndrome,” Journal of Biomedicine and Biotechnology, vol. 2011, Article ID 549107, 14 pages, 2011. © 2011 Tegan N. Lavoie et al. | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Biological Engineering | en_US |
dc.contributor.approver | Nguyen, Cuong Q. | |
dc.contributor.mitauthor | Nguyen, Cuong Q. | |
dc.relation.journal | Journal of Biomedicine and Biotechnology | en_US |
dc.eprint.version | Final published version | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dspace.orderedauthors | Lavoie, Tegan N.; Lee, Byung Ha; Nguyen, Cuong Q. | en |
mit.license | PUBLISHER_CC | en_US |
mit.metadata.status | Complete | |