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231224s2017 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2017.04.003
|2 doi
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|a pubmed25n0902.xml
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|a eng
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|a Kiripolsky, Jeremy
|e verfasserin
|4 aut
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|a Innate immunity in Sjögren's syndrome
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|c 2017
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
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|a ƒa Online-Ressource
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|a Date Completed 06.11.2017
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|a Date Revised 27.03.2024
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2017 Elsevier Inc. All rights reserved.
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|a Sjögren's syndrome (SS) is an autoimmune disease of exocrine tissue that primarily affects women. Although patients typically experience xerostomia and xerophthalmia, numerous systemic disease manifestations are seen. Innate immune hyperactivity is integral to many autoimmune diseases, including SS. Results from SS mouse models suggest that innate immune dysregulation drives disease and this is a seminal event in SS pathogenesis. Findings in SS patients corroborate those in mouse models, as innate immune cells and pathways are dysregulated both in exocrine tissue and in peripheral blood. We will review the role of the innate immune system in SS pathogenesis. We will discuss the etiology of SS with an emphasis on innate immune dysfunction. Moreover, we will review the innate cells that mediate inflammation in SS, the pathways implicated in disease, and the potential mechanisms governing their dysregulation. Finally, we will discuss emerging therapeutic approaches to target dysregulated innate immune signaling in SS
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|a Journal Article
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|a Review
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|a Research Support, Non-U.S. Gov't
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|a A253
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|a Innate immunity
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|a Sjögren's syndrome
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|a Submandibular gland
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|a Toll-like receptor
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1 |
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|a McCabe, Liam G
|e verfasserin
|4 aut
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|a Kramer, Jill M
|e verfasserin
|4 aut
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 182(2017) vom: 15. Sept., Seite 4-13
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|g volume:182
|g year:2017
|g day:15
|g month:09
|g pages:4-13
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|u http://dx.doi.org/10.1016/j.clim.2017.04.003
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