Anti-Siglec-15 Antibody Prevents Marked Bone Loss after Acute Spinal Cord Injury-Induced Immobilization in Rats

被引:1
|
作者
Peng, Yuanzhen [1 ]
Langermann, Solomon [2 ]
Kothari, Priyanka [2 ]
Liu, Linda [2 ]
Zhao, Wei [1 ]
Hu, Yizhong [3 ]
Chen, Zihao [4 ]
de Lima Perini, Mariana Moraes [5 ]
Li, Jiliang [5 ]
Cao, Jay [6 ]
Guo, X. Edward
Chen, Lieping [2 ,7 ]
Bauman, William A. [1 ,8 ,9 ]
Qin, Weiping [1 ,8 ,10 ]
机构
[1] James J Peters Vet Affairs Med Ctr, Spinal Cord Damage Res Ctr, Bronx, NY 10468 USA
[2] NextCure Inc, Beltsville, MD USA
[3] Columbia Univ, Dept Biomed Engn, New York, NY USA
[4] Brown Univ, Dept Biotechnol, Providence, RI USA
[5] Indiana Univ Purdue Univ, Sch Sci, Indianapolis, IN USA
[6] USDA ARS, Grand Forks Human Nutr Res Ctr, Grand Forks, ND USA
[7] Yale Univ, Canc Res Immunobiol & Med, Sch Med, New Haven, CT USA
[8] Icahn Sch Med Mt Sinai, Dept Med Rehabil & Human Performance, New York, NY USA
[9] Icahn Sch Med Mt Sinai, Rehabil & Human Performance, New York, NY USA
[10] James J Peters Vet Affairs Med Ctr, 130 West Kingsbridge Rd, Bronx, NY 10468 USA
关键词
BONE FORMATION; BONE RESORPTION; IMMOBILIZATION; SIGLEC-15; SPINAL CORD INJURY; QUANTITATIVE COMPUTED-TOMOGRAPHY; HIGH-DOSE METHYLPREDNISOLONE; LOW-INTENSITY VIBRATION; POSTMENOPAUSAL WOMEN; MINERAL DENSITY; GENE-EXPRESSION; PARATHYROID-HORMONE; RISK-FACTORS; OSTEOPOROSIS; MUSCLE;
D O I
10.1002/jbm4.10825
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rapid and extensive sublesional bone loss after spinal cord injury (SCI) is a difficult medical problem that has been refractory to available interventions except the antiresorptive agent denosumab (DMAB). While DMAB has shown some efficacy in inhibiting bone loss, its concurrent inhibition of bone formation limits its use. Sialic acid-binding immunoglobulin-like lectin (Siglec)-15 is expressed on the cell surface of mature osteoclasts. Anti-Siglec-15 antibody (Ab) has been shown to inhibit osteoclast maturation and bone resorption while maintaining osteoblast activity, which is distinct from current antiresorptive agents that inhibit the activity of both osteoclasts and osteoblasts. The goal of the present study is to test a Siglec-15 Ab (NP159) as a new treatment option to prevent bone loss in an acute SCI model. To this end, 4-month-old male Wistar rats underwent complete spinal cord transection and were treated with either vehicle or NP159 at 20 mg/kg once every 2 weeks for 8 weeks. SCI results in significant decreases in bone mineral density (BMD, similar to 18.7%), trabecular bone volume (similar to 43.1%), trabecular connectivity (similar to 59.7%), and bone stiffness (similar to 76.3%) at the distal femur. Treatment with NP159 almost completely prevents the aforementioned deterioration of bone after SCI. Blood and histomorphometric analyses revealed that NP159 is able to greatly inhibit bone resorption while maintaining bone formation after acute SCI. In ex vivo cultures of bone marrow cells, NP159 reduces osteoclastogenesis while increasing osteoblastogenesis. In summary, treatment with NP159 almost fully prevents sublesional loss of BMD and metaphysis trabecular bone volume and preserves bone strength in a rat model of acute SCI. Because of its unique ability to reduce osteoclastogenesis and bone resorption while promoting osteoblastogenesis to maintain bone formation, Siglec-15 Ab may hold greater promise as a therapeutic agent, compared with the exclusively antiresorptive or anabolic agents that are currently used, in mitigating the striking bone loss that occurs after SCI or other conditions associated with severe immobilization. (c) 2023 The Authors. JBMR Plus published byWiley Periodicals LLC on behalf of American Society for Bone and Mineral Research. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.
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页数:15
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