Type I IFN signature in primary Sjögren's syndrome patients

Expert Rev Clin Immunol. 2014 Apr;10(4):457-67. doi: 10.1586/1744666X.2014.876364. Epub 2014 Jan 22.

Abstract

Primary Sjögren's syndrome (pSS) is a systemic autoimmune disease characterized by lymphocytic infiltrates in salivary and lacrimal glands. Clinical manifestations range from ocular and oral dryness to vasculitis and severe fatigue. pSS is a disease with heterogeneous symptoms and a variable response to the available treatment. Recently, a key role for Interferon (IFN) type I has been implicated in the pathogenesis of pSS. As type I IFN consists of 17 different subtypes, it cannot be easily assessed using a conventional ELISA. Therefore the expression of type I IFN inducible genes--the so-called type I IFN signature--is assessed in salivary gland tissue and blood from patients as a readout for type I IFN activity. In this review we discuss the potential of type I IFN as a novel biomarker for disease activity, subclassification of patients, prediction of therapy response and most importantly as a target for therapeutic intervention.

Publication types

  • Review

MeSH terms

  • Biomarkers / analysis*
  • Humans
  • Interferon Type I / analysis
  • Interferon Type I / biosynthesis*
  • Interferon Type I / immunology
  • Salivary Glands / immunology
  • Salivary Glands / metabolism
  • Sjogren's Syndrome / genetics
  • Sjogren's Syndrome / immunology*
  • Transcriptome*

Substances

  • Biomarkers
  • Interferon Type I