RANKL is a therapeutic target of bone destruction in rheumatoid arthritis [version 1; peer review: 2 approved]

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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Main Author: Sakae Tanaka
Format: Article
Language:English
Published: F1000 Research Ltd 2019-04-01
Series:F1000Research
Online Access:https://f1000research.com/articles/8-533/v1
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spelling doaj-f0c1a68e75764336b5e68a50fa9843422020-11-25T03:46:07ZengF1000 Research LtdF1000Research2046-14022019-04-01810.12688/f1000research.17296.118910RANKL is a therapeutic target of bone destruction in rheumatoid arthritis [version 1; peer review: 2 approved]Sakae Tanaka0Department of Orthopaedic Surgery, Faculty of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, JapanAlthough 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.https://f1000research.com/articles/8-533/v1
collection DOAJ
language English
format Article
sources DOAJ
author Sakae Tanaka
spellingShingle Sakae Tanaka
RANKL is a therapeutic target of bone destruction in rheumatoid arthritis [version 1; peer review: 2 approved]
F1000Research
author_facet Sakae Tanaka
author_sort Sakae Tanaka
title RANKL is a therapeutic target of bone destruction in rheumatoid arthritis [version 1; peer review: 2 approved]
title_short RANKL is a therapeutic target of bone destruction in rheumatoid arthritis [version 1; peer review: 2 approved]
title_full RANKL is a therapeutic target of bone destruction in rheumatoid arthritis [version 1; peer review: 2 approved]
title_fullStr RANKL is a therapeutic target of bone destruction in rheumatoid arthritis [version 1; peer review: 2 approved]
title_full_unstemmed RANKL is a therapeutic target of bone destruction in rheumatoid arthritis [version 1; peer review: 2 approved]
title_sort rankl is a therapeutic target of bone destruction in rheumatoid arthritis [version 1; peer review: 2 approved]
publisher F1000 Research Ltd
series F1000Research
issn 2046-1402
publishDate 2019-04-01
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.
url https://f1000research.com/articles/8-533/v1
work_keys_str_mv AT sakaetanaka ranklisatherapeutictargetofbonedestructioninrheumatoidarthritisversion1peerreview2approved
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