Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8721543 | Clinical Immunology | 2017 | 10 Pages |
Abstract
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.
Keywords
PDCTNFPAMPMCP-1IBDTLRGM-CSFPRRDAMPNLRSGECA253PSSPGNlncRNASSSLPSMCMVSMGRegulated on Activation, Normal T Expressed and SecretedECMnatural killermicro RNAlong noncoding RNAsRheumatoid arthritisanti-nuclear antibodiesTight junctionANApathogen-associated molecular patternEBVInnate immunityinterferonIFNBAFFInflammatory bowel diseaseToll-like receptorDendritic cellPlasmacytoid dendritic cellSjögren's syndromePrimary Sjögren's syndromeCMVcytomegalovirusMurine cytomegalovirusB-cell activating factorSubmandibular glandtumor necrosis factorTRAILSystemic lupus erythematosusSLElipopolysaccharideTNF-related apoptosis inducing ligandExtracellular matrixgranulocyte macrophage colony-stimulating factorRANTESMiRNAHepatitis C virusHCVEpstein barr virusMonocyte chemotactic protein-1poly(I:C)Peptidoglycanpattern recognition receptor
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Authors
Jeremy Kiripolsky, Liam G. McCabe, Jill M. Kramer,