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RANKL is a therapeutic target of bone destruction in rheumatoid arthritis

Although remarkable advances have been made in the treatment of rheumatoid arthritis (RA), novel therapeutic options with different mechanisms of action and fewer side effects have been expected. Recent studies have demonstrated that bone-resorbing osteoclasts are critically involved in the bone des...

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Autor principal: Tanaka, Sakae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480939/
https://www.ncbi.nlm.nih.gov/pubmed/31069051
http://dx.doi.org/10.12688/f1000research.17296.1
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author Tanaka, Sakae
author_facet Tanaka, Sakae
author_sort Tanaka, Sakae
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description Although remarkable advances have been made in the treatment of rheumatoid arthritis (RA), novel therapeutic options with different mechanisms of action and fewer side effects have been expected. Recent studies have demonstrated that bone-resorbing osteoclasts are critically involved in the bone destruction associated with RA. Denosumab, a human antibody against receptor activator of nuclear factor-kappa B ligand (RANKL), efficiently suppressed the progression of bone erosion in patients with RA by suppressing osteoclast differentiation and activation in several clinical studies, although it had no effect on inflammation or cartilage destruction. Denosumab, in combination with anti-rheumatic drugs, is considered a pivotal therapeutic option for the prevention of bone destruction in RA.
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spelling pubmed-64809392019-05-07 RANKL is a therapeutic target of bone destruction in rheumatoid arthritis Tanaka, Sakae F1000Res Review Although remarkable advances have been made in the treatment of rheumatoid arthritis (RA), novel therapeutic options with different mechanisms of action and fewer side effects have been expected. Recent studies have demonstrated that bone-resorbing osteoclasts are critically involved in the bone destruction associated with RA. Denosumab, a human antibody against receptor activator of nuclear factor-kappa B ligand (RANKL), efficiently suppressed the progression of bone erosion in patients with RA by suppressing osteoclast differentiation and activation in several clinical studies, although it had no effect on inflammation or cartilage destruction. Denosumab, in combination with anti-rheumatic drugs, is considered a pivotal therapeutic option for the prevention of bone destruction in RA. F1000 Research Limited 2019-04-23 /pmc/articles/PMC6480939/ /pubmed/31069051 http://dx.doi.org/10.12688/f1000research.17296.1 Text en Copyright: © 2019 Tanaka S http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Tanaka, Sakae
RANKL is a therapeutic target of bone destruction in rheumatoid arthritis
title RANKL is a therapeutic target of bone destruction in rheumatoid arthritis
title_full RANKL is a therapeutic target of bone destruction in rheumatoid arthritis
title_fullStr RANKL is a therapeutic target of bone destruction in rheumatoid arthritis
title_full_unstemmed RANKL is a therapeutic target of bone destruction in rheumatoid arthritis
title_short RANKL is a therapeutic target of bone destruction in rheumatoid arthritis
title_sort rankl is a therapeutic target of bone destruction in rheumatoid arthritis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480939/
https://www.ncbi.nlm.nih.gov/pubmed/31069051
http://dx.doi.org/10.12688/f1000research.17296.1
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