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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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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1724507795548536832 |