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dc.contributor.authorMoorthy, Arumugam
dc.contributor.authorSamarasinghe, Harini
dc.date.accessioned2024-05-15T13:33:46Z
dc.date.available2024-05-15T13:33:46Z
dc.date.issued2024-05-02
dc.identifier.citationByravan, S., Samarasinghe, H., Yuan, J. S. J., Tahir, S. H., Moorthy, A., & Tahir, H. (2024). From bench to bedside- is there a role of IL-17 drugs in rheumatoid arthritis?. Expert opinion on investigational drugs, 10.1080/13543784.2024.2351505. Advance online publication. https://doi.org/10.1080/13543784.2024.2351505en_US
dc.identifier.other10.1080/13543784.2024.2351505
dc.identifier.urihttp://hdl.handle.net/20.500.12904/18607
dc.description.abstractIntroduction: IL-17 has been described as a pro-inflammatory cytokine that is relevant in the seronegative spondylarthritides with IL-17 targeted therapies being licensed for their treatment.There is evidence to demonstrate that IL-17 is found in RA joints and contributes to the pro-inflammatory cascade. This results in synovial hyperplasia and osteoclastogenesis thus causing joint destruction and bony erosions. Areas covered: This review article summarizes trials that have studied the use of IL-17 targeted therapies in RA patients who have failed conventional synthetic disease-modifying therapy (C-DMARDS) and biologic DMARDS. Expert opinion: The trials that have studied IL-17 inhibitors in RA patients have only shown a modest improvement in disease activity. In several trials, the primary endpoint was not achieved whilst in others, when comparing with existing licensed biologics for RA, did not demonstrate any superiority.Tissue Necrosis Factor-alpha (TNF-α) likely plays more of a pivotal role in the pathogenesis of RA with IL-17 having a synergistic effect. Therefore, in our opinion, IL-17 inhibitors as an independent therapy for RA are less likely to provide a cost-effective benefit. There may be scope to potentially combine it with TNF-α-inhibitors (TNF-i), but this requires further research especially with the potential concerns related to increased immunosuppression.
dc.description.urihttps://www.tandfonline.com/doi/full/10.1080/13543784.2024.2351505en_US
dc.language.isoenen_US
dc.subjectIL-17 inhibitorsen_US
dc.subjectTNF inhibitorsen_US
dc.subjectbiologicsen_US
dc.subjectpathophysiologyen_US
dc.subjectrheumatoid arthritisen_US
dc.subjecttrialsen_US
dc.titleFrom bench to bedside- is there a role of IL-17 drugs in rheumatoid arthritis?en_US
dc.typeArticleen_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US
rioxxterms.versionNAen_US
rioxxterms.versionofrecordhttps://doi.org/10.1080/13543784.2024.2351505en_US
rioxxterms.typeJournal Article/Reviewen_US
refterms.panelUnspecifieden_US
atmire.accessrights
html.description.abstractIntroduction: IL-17 has been described as a pro-inflammatory cytokine that is relevant in the seronegative spondylarthritides with IL-17 targeted therapies being licensed for their treatment.There is evidence to demonstrate that IL-17 is found in RA joints and contributes to the pro-inflammatory cascade. This results in synovial hyperplasia and osteoclastogenesis thus causing joint destruction and bony erosions. Areas covered: This review article summarizes trials that have studied the use of IL-17 targeted therapies in RA patients who have failed conventional synthetic disease-modifying therapy (C-DMARDS) and biologic DMARDS. Expert opinion: The trials that have studied IL-17 inhibitors in RA patients have only shown a modest improvement in disease activity. In several trials, the primary endpoint was not achieved whilst in others, when comparing with existing licensed biologics for RA, did not demonstrate any superiority.Tissue Necrosis Factor-alpha (TNF-α) likely plays more of a pivotal role in the pathogenesis of RA with IL-17 having a synergistic effect. Therefore, in our opinion, IL-17 inhibitors as an independent therapy for RA are less likely to provide a cost-effective benefit. There may be scope to potentially combine it with TNF-α-inhibitors (TNF-i), but this requires further research especially with the potential concerns related to increased immunosuppression.en_US
rioxxterms.funder.project94a427429a5bcfef7dd04c33360d80cden_US


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