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Review
. 2022 Oct 20;3(3):95-102.
doi: 10.2478/rir-2022-0017. eCollection 2022 Oct.

JAK/STAT Pathway Targeting in Primary Sjögren Syndrome

Affiliations
Review

JAK/STAT Pathway Targeting in Primary Sjögren Syndrome

Saviana Gandolfo et al. Rheumatol Immunol Res. .

Abstract

Primary Sjögren's syndrome (pSS) is an autoimmune systemic disease mainly affecting exocrine glands and resulting in disabling symptoms, as dry eye and dry mouth. Mechanisms underlying pSS pathogenesis are intricate, involving multiplanar and, at the same time, interlinked levels, e.g., genetic predisposition, epigenetic modifications and the dysregulation of both immune system and glandular-resident cellular pathways, mainly salivary gland epithelial cells. Unravelling the biological and molecular complexity of pSS is still a great challenge but much progress has been made in recent years in basic and translational research field, allowing the identification of potential novel targets for therapy development. Despite such promising novelties, however, none therapy has been specifically approved for pSS treatment until now. In recent years, growing evidence has supported the modulation of Janus kinases (JAK) - signal transducers and activators of transcription (STAT) pathways as treatment strategy immune mediated diseases. JAK-STAT pathway plays a crucial role in autoimmunity and systemic inflammation, being involved in signal pathways of many cytokines. This review aims to report the state-of-the-art about the role of JAK-STAT pathway in pSS, with particular focus on available research and clinical data regarding the use of JAK inhibitors in pSS.

Keywords: JAK molecules; STAT molecules; Sjögren's syndrome; cytokines.

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Conflict of interest statement

Conflict of Interest Francesco Ciccia is an Editorial Board Member of the journal. This article was subject to the journal's standard procedures, with peer review handled independently of this member and his research group.

Figures

Figure 1
Figure 1
Main cytokines signaling through JAK-STAT involved in pSS pathogenesis.

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