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New developments in systemic lupus erythematosus

In this review, the results of recent and ongoing clinical trials in patients with SLE are discussed. After many unsuccessful trials in the past decade, belimumab was the first biologic specifically designed for SLE that met its primary end point. At the same time, studies on the pathophysiology of...

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Autores principales: Tsang-A-Sjoe, Michel W. P., Bultink, Irene E. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709564/
https://www.ncbi.nlm.nih.gov/pubmed/34951924
http://dx.doi.org/10.1093/rheumatology/keab498
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author Tsang-A-Sjoe, Michel W. P.
Bultink, Irene E. M.
author_facet Tsang-A-Sjoe, Michel W. P.
Bultink, Irene E. M.
author_sort Tsang-A-Sjoe, Michel W. P.
collection PubMed
description In this review, the results of recent and ongoing clinical trials in patients with SLE are discussed. After many unsuccessful trials in the past decade, belimumab was the first biologic specifically designed for SLE that met its primary end point. At the same time, studies on the pathophysiology of SLE have further elucidated the pathways involved in the disease, which has led to the identification of new possible therapeutics and has encouraged the initiation of new trials. These new drugs include biologics that target B cells, T cells and type 1 interferons, and small molecules that inhibit kinases. Other therapeutics aim to restore immunological balance by restoring tolerance. Results from phase II and even phase III trials are promising and it is likely that some of the therapeutics discussed will receive approval in the following years. Hopefully, this will allow for more tailor-made medicine for SLE patients in the future.
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spelling pubmed-87095642022-01-04 New developments in systemic lupus erythematosus Tsang-A-Sjoe, Michel W. P. Bultink, Irene E. M. Rheumatology (Oxford) Supplement Papers In this review, the results of recent and ongoing clinical trials in patients with SLE are discussed. After many unsuccessful trials in the past decade, belimumab was the first biologic specifically designed for SLE that met its primary end point. At the same time, studies on the pathophysiology of SLE have further elucidated the pathways involved in the disease, which has led to the identification of new possible therapeutics and has encouraged the initiation of new trials. These new drugs include biologics that target B cells, T cells and type 1 interferons, and small molecules that inhibit kinases. Other therapeutics aim to restore immunological balance by restoring tolerance. Results from phase II and even phase III trials are promising and it is likely that some of the therapeutics discussed will receive approval in the following years. Hopefully, this will allow for more tailor-made medicine for SLE patients in the future. Oxford University Press 2021-12-24 /pmc/articles/PMC8709564/ /pubmed/34951924 http://dx.doi.org/10.1093/rheumatology/keab498 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 (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, [br]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
Tsang-A-Sjoe, Michel W. P.
Bultink, Irene E. M.
New developments in systemic lupus erythematosus
title New developments in systemic lupus erythematosus
title_full New developments in systemic lupus erythematosus
title_fullStr New developments in systemic lupus erythematosus
title_full_unstemmed New developments in systemic lupus erythematosus
title_short New developments in systemic lupus erythematosus
title_sort new developments in systemic lupus erythematosus
topic Supplement Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709564/
https://www.ncbi.nlm.nih.gov/pubmed/34951924
http://dx.doi.org/10.1093/rheumatology/keab498
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