Innate immunity in Sjogren's syndrome

被引:62
作者
Kiripolsky, Jeremy [1 ]
McCabe, Liam G. [1 ,3 ]
Kramer, Jill M. [1 ,2 ]
机构
[1] SUNY Buffalo, Sch Dent Med, Dept Oral Biol, 3435 Main St,211 Foster Hall, Buffalo, NY 14214 USA
[2] SUNY Buffalo, Sch Dent Med, Dept Oral Diagnost Sci, Buffalo, NY 14214 USA
[3] Immco Diagnost Inc, 60 Pineview Dr, Amherst, NY USA
关键词
Sjogren's syndrome; Innate immunity; A253; Submandibular gland; Toll-like receptor; GLAND EPITHELIAL-CELLS; TOLL-LIKE RECEPTORS; MINOR SALIVARY-GLANDS; LONG NONCODING RNAS; PLASMACYTOID DENDRITIC CELLS; SYSTEMIC-LUPUS-ERYTHEMATOSUS; ECTOPIC LYMPHOID NEOGENESIS; SYNDROME (S[!text type='JS']JS[!/text])-LIKE DISEASE; TIGHT JUNCTION STRUCTURE; B-CELLS;
D O I
10.1016/j.clim.2017.04.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Sjogren'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. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:4 / 13
页数:10
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