Adenovirus Encoding Human Platelet-Derived Growth Factor-B Delivered to Alveolar Bone Defects Exhibits Safety and Biodistribution Profiles Favorable for Clinical Use

被引:64
作者
Chang, Po-Chun [1 ,2 ]
Cirelli, Joni A. [1 ]
Jin, Qiming [1 ]
Seol, Yang-Jo [1 ,3 ]
Sugai, James V. [1 ]
D'Silva, Nisha J. [1 ]
Danciu, Theodora E. [1 ]
Chandler, Lois A. [4 ]
Sosnowski, Barbara A. [4 ]
Giannobile, William V. [1 ,2 ]
机构
[1] Univ Michigan, Dept Periodont & Oral Med, Sch Dent, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Biomed Engn, Coll Engn, Ann Arbor, MI 48109 USA
[3] Seoul Natl Univ, Sch Dent, Dept Periodontol, Seoul 110749, South Korea
[4] Tissue Repair Co, San Diego, CA 92121 USA
关键词
GENE-TRANSFER; INTRAVENOUS-INJECTION; PDGF-ALPHA; FACTOR-I; VECTORS; THERAPY; MOUSE; REGENERATION; FIBROBLASTS; COMBINATION;
D O I
10.1089/hum.2008.114
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Platelet-derived growth factor (PDGF) gene therapy offers promise for tissue engineering of tooth-supporting alveolar bone defects. To date, limited information exists regarding the safety profile and systemic biodistribution of PDGF gene therapy vectors when delivered locally to periodontal osseous defects. The aim of this preclinical study was to determine the safety profile of adenovirus encoding the PDGF-B gene (AdPDGF-B) delivered in a collagen matrix to periodontal lesions. Standardized alveolar bone defects were created in rats, followed by delivery of matrix alone or containing AdPDGF-B at 5.5 x 10(8) or 5.5 x 10(9) plaque-forming units/ml. The regenerative response was confirmed histologically. Gross clinical observations, hematology, and blood chemistries were monitored to evaluate systemic involvement. Bioluminescence and quantitative polymerase chain reaction were used to assess vector biodistribution. No significant histopathological changes were noted during the investigation. Minor alterations in specific hematological and blood chemistries were seen; however, most parameters were within the normal range for all groups. Bioluminescence analysis revealed vector distribution at the axillary lymph nodes during the first 2 weeks with subsequent return to baseline levels. AdPDGF-B was well contained within the localized osseous defect area without viremia or distant organ involvement. These results indicate that AdPDGF-B delivered in a collagen matrix exhibits acceptable safety profiles for possible use in human clinical studies.
引用
收藏
页码:486 / 496
页数:11
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