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JAK1 selective inhibitors for the treatment of spondyloarthropathies

As our understanding of the pathogenesis of SpA improves, focus has turned to the role janus kinase (JAK)-mediated signal transduction and inhibiting its actions as a therapeutic mechanism. Small molecule inhibitors of JAK exist, with variable selectivity for the different JAK isoforms. Less selecti...

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Detalles Bibliográficos
Autores principales: White, Jonathan P E, Coates, Laura C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8098108/
https://www.ncbi.nlm.nih.gov/pubmed/33950224
http://dx.doi.org/10.1093/rheumatology/keaa815
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author White, Jonathan P E
Coates, Laura C
author_facet White, Jonathan P E
Coates, Laura C
author_sort White, Jonathan P E
collection PubMed
description As our understanding of the pathogenesis of SpA improves, focus has turned to the role janus kinase (JAK)-mediated signal transduction and inhibiting its actions as a therapeutic mechanism. Small molecule inhibitors of JAK exist, with variable selectivity for the different JAK isoforms. Less selective JAK inhibitors have variable efficacy and safety profiles, prompting the investigation of selective JAK1 inhibition. In this review, we summarize the current phase 2 and 3 clinical trial data, evaluating the use of JAK1 selective inhibitors in the treatment of SpA, particularly AS and PsA. Selective JAK1 inhibition offers a promising therapeutic approach, however further longer-term trials are needed to fully establish their efficacy and safety at higher doses, and their use in the greater continuum of SpA.
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spelling pubmed-80981082021-05-10 JAK1 selective inhibitors for the treatment of spondyloarthropathies White, Jonathan P E Coates, Laura C Rheumatology (Oxford) Supplement Papers As our understanding of the pathogenesis of SpA improves, focus has turned to the role janus kinase (JAK)-mediated signal transduction and inhibiting its actions as a therapeutic mechanism. Small molecule inhibitors of JAK exist, with variable selectivity for the different JAK isoforms. Less selective JAK inhibitors have variable efficacy and safety profiles, prompting the investigation of selective JAK1 inhibition. In this review, we summarize the current phase 2 and 3 clinical trial data, evaluating the use of JAK1 selective inhibitors in the treatment of SpA, particularly AS and PsA. Selective JAK1 inhibition offers a promising therapeutic approach, however further longer-term trials are needed to fully establish their efficacy and safety at higher doses, and their use in the greater continuum of SpA. Oxford University Press 2021-05-05 /pmc/articles/PMC8098108/ /pubmed/33950224 http://dx.doi.org/10.1093/rheumatology/keaa815 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Rheumatology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Supplement Papers
White, Jonathan P E
Coates, Laura C
JAK1 selective inhibitors for the treatment of spondyloarthropathies
title JAK1 selective inhibitors for the treatment of spondyloarthropathies
title_full JAK1 selective inhibitors for the treatment of spondyloarthropathies
title_fullStr JAK1 selective inhibitors for the treatment of spondyloarthropathies
title_full_unstemmed JAK1 selective inhibitors for the treatment of spondyloarthropathies
title_short JAK1 selective inhibitors for the treatment of spondyloarthropathies
title_sort jak1 selective inhibitors for the treatment of spondyloarthropathies
topic Supplement Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8098108/
https://www.ncbi.nlm.nih.gov/pubmed/33950224
http://dx.doi.org/10.1093/rheumatology/keaa815
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