Siglec-15-targeting therapy protects against glucocorticoid-induced osteoporosis of growing skeleton in juvenile rats.


Journal

Bone
ISSN: 1873-2763
Titre abrégé: Bone
Pays: United States
ID NLM: 8504048

Informations de publication

Date de publication:
06 2020
Historique:
received: 14 02 2020
revised: 12 03 2020
accepted: 23 03 2020
pubmed: 29 3 2020
medline: 16 6 2022
entrez: 29 3 2020
Statut: ppublish

Résumé

Effective treatment of juvenile osteoporosis, which is frequently caused by glucocorticoid (GC) therapy, has not been established due to limited data regarding the efficacy and adverse effects of antiresorptive therapies on the growing skeleton. We previously demonstrated that sialic acid-binding immunoglobulin-like lectin 15 (Siglec-15) targeting therapy, which interferes with osteoclast terminal differentiation in the secondary, but not primary, spongiosa, increased bone mass without adverse effects on skeletal growth, whereas bisphosphonate, a first-line treatment for osteoporosis, increased bone mass but impaired long bone growth in healthy growing rats. In the present study, we investigated the efficacy of anti-Siglec-15 neutralizing antibody (Ab) therapy against GC-induced osteoporosis in a growing rat model. GC decreased bone mass and deteriorated mechanical properties of bone, due to a disproportionate increase in bone resorption. Both anti-Siglec-15 Ab and alendronate (ALN) showed protective effects against GC-induced bone loss by suppressing bone resorption, which was more pronounced with anti-Siglec-15 Ab treatment, possibly due to a reduced negative impact on bone formation. ALN induced histological abnormalities in the growth plate and morphological abnormalities in the long bone metaphysis but did not cause significant growth retardation. Conversely, anti-Siglec-15 Ab did not show any negative impact on the growth plate and preserved normal osteoclast and chondroclast function at the primary spongiosa. Taken together, these results suggest that anti-Siglec-15 targeting therapy could be a safe and efficacious prophylactic therapy for GC-induced osteoporosis in juvenile patients.

Identifiants

pubmed: 32217159
pii: S8756-3282(20)30111-3
doi: 10.1016/j.bone.2020.115331
pii:
doi:

Substances chimiques

Glucocorticoids 0
Sialic Acid Binding Immunoglobulin-like Lectins 0
Alendronate X1J18R4W8P

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

115331

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest Conflicts of interest: M.T. has received research funding from Daiichi Sankyo Co., Ltd., which provided the materials being tested in the present study. C.F., E.T., Y.H., and A.O. are employees of Daiichi Sankyo Co., Ltd. All other authors state that they have no conflict of interest.

Auteurs

Dai Sato (D)

Department of Orthopaedic Surgery, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo 060-8638, Japan.

Masahiko Takahata (M)

Department of Orthopaedic Surgery, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo 060-8638, Japan. Electronic address: takamasa@med.hokudai.ac.jp.

Masahiro Ota (M)

Department of Orthopaedic Surgery, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo 060-8638, Japan.

Chie Fukuda (C)

Specialty Medicine Research Laboratories I, Daiichi Sankyo Co., Ltd., Tokyo, Japan.

Tomoka Hasegawa (T)

Hokkaido University, Department of Developmental Biology of Hard Tissue, Graduate School of Dental Medicine, Sapporo, Japan.

Tomomaya Yamamoto (T)

Hokkaido University, Department of Developmental Biology of Hard Tissue, Graduate School of Dental Medicine, Sapporo, Japan.

Norio Amizuka (N)

Hokkaido University, Department of Developmental Biology of Hard Tissue, Graduate School of Dental Medicine, Sapporo, Japan.

Eisuke Tsuda (E)

Specialty Medicine Research Laboratories I, Daiichi Sankyo Co., Ltd., Tokyo, Japan.

Akiko Okada (A)

Specialty Medicine Research Laboratories I, Daiichi Sankyo Co., Ltd., Tokyo, Japan.

Yoshiharu Hiruma (Y)

Pharmacovigilance Department, Daiichi Sankyo Co., Ltd., Tokyo, Japan.

Ryo Fujita (R)

Department of Orthopaedic Surgery, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo 060-8638, Japan.

Norimasa Iwasaki (N)

Department of Orthopaedic Surgery, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo 060-8638, Japan.

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Classifications MeSH