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Novel Therapeutic Targets in Axial Spondyloarthritis

PURPOSE OF REVIEW: Axial spondyloarthritis remains an area of significant unmet clinical need with only two immune pathways currently targeted by licenced therapies compared to other immune-mediated inflammatory joint disorders such as rheumatoid arthritis where a multitude of therapeutic options ar...

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Autores principales: Worth, Claudia, Bowness, Paul, Hussein Al-Mossawi, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5978800/
https://www.ncbi.nlm.nih.gov/pubmed/29938195
http://dx.doi.org/10.1007/s40674-018-0095-1
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author Worth, Claudia
Bowness, Paul
Hussein Al-Mossawi, M.
author_facet Worth, Claudia
Bowness, Paul
Hussein Al-Mossawi, M.
author_sort Worth, Claudia
collection PubMed
description PURPOSE OF REVIEW: Axial spondyloarthritis remains an area of significant unmet clinical need with only two immune pathways currently targeted by licenced therapies compared to other immune-mediated inflammatory joint disorders such as rheumatoid arthritis where a multitude of therapeutic options are available. This review will look at emerging therapeutic targets in axial spondyloarthritis beyond the neutralisation of IL-17A and TNF by monoclonal antibodies. RECENT FINDINGS: Several promising targets are in various stages of pre-clinical and clinical development in axial spondyloarthritis. These include small molecule approaches to target transcription factors, epigenetic modification and intracellular modulation of cytokine signalling by kinase inhibition. GM-CSF has also emerged as a potential driver of inflammation. SUMMARY: A number of novel and promising therapeutic options are in various stages of development in axial spondyloarthritis. The Janus kinase inhibitors have shown great promise in other immune-mediated inflammatory disorders and will be an exciting addition to the axial spondyloarthritis field as the first oral disease-modifying agents. GM-CSF blockade also shows great promise since antibodies for neutralising this cytokine are safe in patients and have shown efficacy in other immune-mediated inflammatory diseases.
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spelling pubmed-59788002018-06-21 Novel Therapeutic Targets in Axial Spondyloarthritis Worth, Claudia Bowness, Paul Hussein Al-Mossawi, M. Curr Treatm Opt Rheumatol Seronegative Arthritis (N Haroon, Section Editor) PURPOSE OF REVIEW: Axial spondyloarthritis remains an area of significant unmet clinical need with only two immune pathways currently targeted by licenced therapies compared to other immune-mediated inflammatory joint disorders such as rheumatoid arthritis where a multitude of therapeutic options are available. This review will look at emerging therapeutic targets in axial spondyloarthritis beyond the neutralisation of IL-17A and TNF by monoclonal antibodies. RECENT FINDINGS: Several promising targets are in various stages of pre-clinical and clinical development in axial spondyloarthritis. These include small molecule approaches to target transcription factors, epigenetic modification and intracellular modulation of cytokine signalling by kinase inhibition. GM-CSF has also emerged as a potential driver of inflammation. SUMMARY: A number of novel and promising therapeutic options are in various stages of development in axial spondyloarthritis. The Janus kinase inhibitors have shown great promise in other immune-mediated inflammatory disorders and will be an exciting addition to the axial spondyloarthritis field as the first oral disease-modifying agents. GM-CSF blockade also shows great promise since antibodies for neutralising this cytokine are safe in patients and have shown efficacy in other immune-mediated inflammatory diseases. Springer International Publishing 2018-04-12 2018 /pmc/articles/PMC5978800/ /pubmed/29938195 http://dx.doi.org/10.1007/s40674-018-0095-1 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Seronegative Arthritis (N Haroon, Section Editor)
Worth, Claudia
Bowness, Paul
Hussein Al-Mossawi, M.
Novel Therapeutic Targets in Axial Spondyloarthritis
title Novel Therapeutic Targets in Axial Spondyloarthritis
title_full Novel Therapeutic Targets in Axial Spondyloarthritis
title_fullStr Novel Therapeutic Targets in Axial Spondyloarthritis
title_full_unstemmed Novel Therapeutic Targets in Axial Spondyloarthritis
title_short Novel Therapeutic Targets in Axial Spondyloarthritis
title_sort novel therapeutic targets in axial spondyloarthritis
topic Seronegative Arthritis (N Haroon, Section Editor)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5978800/
https://www.ncbi.nlm.nih.gov/pubmed/29938195
http://dx.doi.org/10.1007/s40674-018-0095-1
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