Abstract |
IL-23 is a cytokine member of the IL-12 superfamily. These heterodimeric cytokines offer broad immune regulatory activity with potential effector function in inflammatory arthritis. IL-23 is a pro-inflammatory cytokine secreted by dendritic cells and macrophages. It plays a key role in both innate and adaptive immunity. By promoting and maintaining T cell differentiation into Th17 T cells, IL-23 is a key player in the pathogenesis of rheumatic diseases. Data from pre-clinical IL-23 knockout models show the major importance of IL-23 in development of arthritis. The induction and maintenance of type 17 cells, which secrete IL-17A and other pro-inflammatory cytokines, contributes to local synovial inflammation and skin inflammation in PsA, and perhaps in RA. Commensurate with this, therapeutic strategies targeting IL-23 have proven efficient in PsA in several studies, albeit not yet in RA.
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Authors | Aurélie Najm, Iain B McInnes |
Journal | Rheumatology (Oxford, England)
(Rheumatology (Oxford))
Vol. 60
Issue Suppl 4
Pg. iv4-iv15
(10 19 2021)
ISSN: 1462-0332 [Electronic] England |
PMID | 34668017
(Publication Type: Editorial, Research Support, Non-U.S. Gov't)
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Copyright | © The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Rheumatology. |
Chemical References |
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Topics |
- Animals
- Arthritis
(drug therapy, immunology, metabolism)
- Humans
- Interleukin-23
(antagonists & inhibitors, metabolism)
- Molecular Targeted Therapy
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