IL-23/IL-17 axis in spondyloarthritis-bench to bedside

Siba P Raychaudhuri; Smriti K. Raychaudhuri

doi:10.1007/s10067-016-3263-4

IL-23/IL-17 axis in spondyloarthritis-bench to bedside

Siba P Raychaudhuri, Smriti K. Raychaudhuri

Rheumatology, Allergy, and Clinical Immunology

Research output: Contribution to journal › Article

19 Scopus citations

Abstract

Cytokines play a critical role in the pathogenesis of psoriatic arthritis, ankylosing spondylitis, and other types of spondyloarthritis (SpA). Besides IFN-γ and TNF-α; IL-23/IL-17 cytokines play a dominant role in the inflammatory and proliferative cascades of SpA. Recently, in a series of elegant experiments using mouse models and human tissues, it has been demonstrated that IL-23-induced Th17 cytokines (IL-17 and IL-22) can contribute to following pathologic events associated with SpA: development of psoriatic plaque, pannus formation in the joint, joint erosion, and new bone formation. In this review article, we have discussed the contributing role of the IL-23/IL-17 cytokine axis in the pathogenesis of PsA and AS. IL-23/IL-17-targeted therapies are very promising for SpA, and we have provided an outline about usefulness of these new groups of biologics in SpA.

Original language	English (US)
Pages (from-to)	1437-1441
Number of pages	5
Journal	Clinical Rheumatology
Volume	35
Issue number	6
DOIs	https://doi.org/10.1007/s10067-016-3263-4
State	Published - Jun 1 2016

Keywords

Ankylosing spoindylitis
IL-17
IL-23
Psoriatic arthritis
Spondyloarthritis
Th17 Cell

ASJC Scopus subject areas

Rheumatology

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Raychaudhuri, S. P., & Raychaudhuri, S. K. (2016). IL-23/IL-17 axis in spondyloarthritis-bench to bedside. Clinical Rheumatology, 35(6), 1437-1441. https://doi.org/10.1007/s10067-016-3263-4

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abstract = "Cytokines play a critical role in the pathogenesis of psoriatic arthritis, ankylosing spondylitis, and other types of spondyloarthritis (SpA). Besides IFN-γ and TNF-α; IL-23/IL-17 cytokines play a dominant role in the inflammatory and proliferative cascades of SpA. Recently, in a series of elegant experiments using mouse models and human tissues, it has been demonstrated that IL-23-induced Th17 cytokines (IL-17 and IL-22) can contribute to following pathologic events associated with SpA: development of psoriatic plaque, pannus formation in the joint, joint erosion, and new bone formation. In this review article, we have discussed the contributing role of the IL-23/IL-17 cytokine axis in the pathogenesis of PsA and AS. IL-23/IL-17-targeted therapies are very promising for SpA, and we have provided an outline about usefulness of these new groups of biologics in SpA.",

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