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Calvarial Model of Bone Augmentation in Rabbit for Assessment of Bone Growth and Neovascularization in Bone Substitution Materials
Published on: August 13, 2019
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Application of AMOR in craniofacial rabbit bone bioengineering.
Marcelo Freire1, Jeong-Ho Choi2, Anthony Nguyen3
1Department of Applied Oral Sciences, The Forsyth Institute, Cambridge, MA, USA ; Department of Infection and Immunity, Harvard School of Dental Medicine, Boston, MA, USA.
Biomed Research International
|February 24, 2015
Summary
Antibody-mediated osseous regeneration (AMOR) uses antibodies to capture bone-building proteins, promoting significant bone repair in rabbit defects. Specific antibody clones are crucial for this novel bone regeneration strategy.
Area of Science:
- Biomaterials Science
- Regenerative Medicine
- Skeletal Biology
Background:
- Tissue repair and regeneration are modulated by endogenous molecular and cellular mediators.
- Antibody-mediated osseous regeneration (AMOR) is a novel strategy for bioengineering bone using antibodies to capture endogenous bone morphogenetic proteins (BMPs).
Purpose of the Study:
- To investigate the feasibility and efficacy of AMOR in a rabbit calvarial defect model.
- To evaluate the role of specific anti-BMP-2 antibody clones in mediating bone regeneration.
Main Methods:
- Utilized a panel of anti-BMP-2 monoclonal antibodies (mAbs) and a polyclonal antibody immobilized on absorbable collagen sponge (ACS).
- Implanted the antibody-loaded ACS into critical-size calvarial defects in rabbits.
- Assessed de novo bone formation using micro-CT imaging, histology, and histomorphometric analysis after 6 weeks.
Main Results:
- Specific anti-BMP-2 mAb clones significantly mediated in vivo bone regeneration in rabbit calvarial defects.
- The reactivity of mAbs to specific epitopes on BMPs appears critical for AMOR efficacy.
- Observed increased localization of BMP-2 protein and osteocalcin expression within defects, indicating BMP accumulation and/or de novo expression.
Conclusions:
- AMOR is a feasible strategy for promoting bone regeneration in rabbit calvarial defects.
- The selection of specific anti-BMP-2 antibody clones targeting critical epitopes is essential for successful AMOR.
- Further preclinical studies in larger animal models are warranted for human translation.

