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Janus kinase-targeting therapies in rheumatology: a mechanisms-based approach

The four Janus kinase (JAK) proteins and seven signal transducer and activator of transcription (STAT) transcription factors mediate intracellular signal transduction downstream of cytokine receptors, which are implicated in the pathology of autoimmune, allergic and inflammatory diseases. Developmen...

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Autores principales: Tanaka, Yoshiya, Luo, Yiming, O’Shea, John J., Nakayamada, Shingo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8730299/
https://www.ncbi.nlm.nih.gov/pubmed/34987201
http://dx.doi.org/10.1038/s41584-021-00726-8
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author Tanaka, Yoshiya
Luo, Yiming
O’Shea, John J.
Nakayamada, Shingo
author_facet Tanaka, Yoshiya
Luo, Yiming
O’Shea, John J.
Nakayamada, Shingo
author_sort Tanaka, Yoshiya
collection PubMed
description The four Janus kinase (JAK) proteins and seven signal transducer and activator of transcription (STAT) transcription factors mediate intracellular signal transduction downstream of cytokine receptors, which are implicated in the pathology of autoimmune, allergic and inflammatory diseases. Development of targeted small-molecule therapies such as JAK inhibitors, which have varied selective inhibitory profiles, has enabled a paradigm shift in the treatment of diverse disorders. JAK inhibitors suppress intracellular signalling mediated by multiple cytokines involved in the pathological processes of rheumatoid arthritis and many other immune and inflammatory diseases, and therefore have the capacity to target multiple aspects of those diseases. In addition to rheumatoid arthritis, JAK inhibition has potential for treatment of autoimmune diseases including systemic lupus erythematosus, spondyloarthritis, inflammatory bowel disease and alopecia areata, in which stimulation of innate immunity activates adaptive immunity, leading to generation of autoreactive T cells and activation and differentiation of B cells. JAK inhibitors are also effective in the treatment of allergic disorders, such as atopic dermatitis, and can even be used for the COVID-19-related cytokine storm. Mechanism-based treatments targeting JAK–STAT pathways have the potential to provide positive outcomes by minimizing the use of glucocorticoids and/or non-specific immunosuppressants in the treatment of systemic immune-mediated inflammatory diseases.
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spelling pubmed-87302992022-01-06 Janus kinase-targeting therapies in rheumatology: a mechanisms-based approach Tanaka, Yoshiya Luo, Yiming O’Shea, John J. Nakayamada, Shingo Nat Rev Rheumatol Review Article The four Janus kinase (JAK) proteins and seven signal transducer and activator of transcription (STAT) transcription factors mediate intracellular signal transduction downstream of cytokine receptors, which are implicated in the pathology of autoimmune, allergic and inflammatory diseases. Development of targeted small-molecule therapies such as JAK inhibitors, which have varied selective inhibitory profiles, has enabled a paradigm shift in the treatment of diverse disorders. JAK inhibitors suppress intracellular signalling mediated by multiple cytokines involved in the pathological processes of rheumatoid arthritis and many other immune and inflammatory diseases, and therefore have the capacity to target multiple aspects of those diseases. In addition to rheumatoid arthritis, JAK inhibition has potential for treatment of autoimmune diseases including systemic lupus erythematosus, spondyloarthritis, inflammatory bowel disease and alopecia areata, in which stimulation of innate immunity activates adaptive immunity, leading to generation of autoreactive T cells and activation and differentiation of B cells. JAK inhibitors are also effective in the treatment of allergic disorders, such as atopic dermatitis, and can even be used for the COVID-19-related cytokine storm. Mechanism-based treatments targeting JAK–STAT pathways have the potential to provide positive outcomes by minimizing the use of glucocorticoids and/or non-specific immunosuppressants in the treatment of systemic immune-mediated inflammatory diseases. Nature Publishing Group UK 2022-01-05 2022 /pmc/articles/PMC8730299/ /pubmed/34987201 http://dx.doi.org/10.1038/s41584-021-00726-8 Text en © Springer Nature Limited 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review Article
Tanaka, Yoshiya
Luo, Yiming
O’Shea, John J.
Nakayamada, Shingo
Janus kinase-targeting therapies in rheumatology: a mechanisms-based approach
title Janus kinase-targeting therapies in rheumatology: a mechanisms-based approach
title_full Janus kinase-targeting therapies in rheumatology: a mechanisms-based approach
title_fullStr Janus kinase-targeting therapies in rheumatology: a mechanisms-based approach
title_full_unstemmed Janus kinase-targeting therapies in rheumatology: a mechanisms-based approach
title_short Janus kinase-targeting therapies in rheumatology: a mechanisms-based approach
title_sort janus kinase-targeting therapies in rheumatology: a mechanisms-based approach
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8730299/
https://www.ncbi.nlm.nih.gov/pubmed/34987201
http://dx.doi.org/10.1038/s41584-021-00726-8
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