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Kinase inhibition in autoimmunity and inflammation

Despite recent advances in the treatment of autoimmune and inflammatory diseases, unmet medical needs in some areas still exist. One of the main therapeutic approaches to alleviate dysregulated inflammation has been to target the activity of kinases that regulate production of inflammatory mediators...

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Detalles Bibliográficos
Autores principales: Zarrin, Ali A., Bao, Katherine, Lupardus, Patrick, Vucic, Domagoj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569567/
https://www.ncbi.nlm.nih.gov/pubmed/33077936
http://dx.doi.org/10.1038/s41573-020-0082-8
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author Zarrin, Ali A.
Bao, Katherine
Lupardus, Patrick
Vucic, Domagoj
author_facet Zarrin, Ali A.
Bao, Katherine
Lupardus, Patrick
Vucic, Domagoj
author_sort Zarrin, Ali A.
collection PubMed
description Despite recent advances in the treatment of autoimmune and inflammatory diseases, unmet medical needs in some areas still exist. One of the main therapeutic approaches to alleviate dysregulated inflammation has been to target the activity of kinases that regulate production of inflammatory mediators. Small-molecule kinase inhibitors have the potential for broad efficacy, convenience and tissue penetrance, and thus often offer important advantages over biologics. However, designing kinase inhibitors with target selectivity and minimal off-target effects can be challenging. Nevertheless, immense progress has been made in advancing kinase inhibitors with desirable drug-like properties into the clinic, including inhibitors of JAKs, IRAK4, RIPKs, BTK, SYK and TPL2. This Review will address the latest discoveries around kinase inhibitors with an emphasis on clinically validated autoimmunity and inflammatory pathways.
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spelling pubmed-75695672020-10-19 Kinase inhibition in autoimmunity and inflammation Zarrin, Ali A. Bao, Katherine Lupardus, Patrick Vucic, Domagoj Nat Rev Drug Discov Review Article Despite recent advances in the treatment of autoimmune and inflammatory diseases, unmet medical needs in some areas still exist. One of the main therapeutic approaches to alleviate dysregulated inflammation has been to target the activity of kinases that regulate production of inflammatory mediators. Small-molecule kinase inhibitors have the potential for broad efficacy, convenience and tissue penetrance, and thus often offer important advantages over biologics. However, designing kinase inhibitors with target selectivity and minimal off-target effects can be challenging. Nevertheless, immense progress has been made in advancing kinase inhibitors with desirable drug-like properties into the clinic, including inhibitors of JAKs, IRAK4, RIPKs, BTK, SYK and TPL2. This Review will address the latest discoveries around kinase inhibitors with an emphasis on clinically validated autoimmunity and inflammatory pathways. Nature Publishing Group UK 2020-10-19 2021 /pmc/articles/PMC7569567/ /pubmed/33077936 http://dx.doi.org/10.1038/s41573-020-0082-8 Text en © Springer Nature Limited 2020 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
Zarrin, Ali A.
Bao, Katherine
Lupardus, Patrick
Vucic, Domagoj
Kinase inhibition in autoimmunity and inflammation
title Kinase inhibition in autoimmunity and inflammation
title_full Kinase inhibition in autoimmunity and inflammation
title_fullStr Kinase inhibition in autoimmunity and inflammation
title_full_unstemmed Kinase inhibition in autoimmunity and inflammation
title_short Kinase inhibition in autoimmunity and inflammation
title_sort kinase inhibition in autoimmunity and inflammation
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569567/
https://www.ncbi.nlm.nih.gov/pubmed/33077936
http://dx.doi.org/10.1038/s41573-020-0082-8
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