Abstract
Background: An anti-CD146 monoclonal antibody, AA98, has been identified as an inhibitor of tumor angiogenesis. To overcome the inherent immunogenicity of murine antibody as well as to facilitate immunotoxin construction, a single chain AA98 VH/L with three-domain fragments was constructed and expressed in mammalian cells. Materials and Methods: The genes of the AA98 heavy chain variable region and the light chain were linked with a modified 12 amino acid sequence that was derived from the heavy chain CH1 region, thus constituting the three-domain antibody VH/L. Soluble AA98 VH/L was produced by mammalian cells and purified by affinity chromatography. The specificity of AA98 VH/L for the CD146 molecule was detected by ELISA, immunofluorescence staining and flow cytometry. Results: AA98 VH/L alone showed anti-angiogenic properties in a chicken chorioallantoic membrane (CAM) assay as the parent mAb AA98 did. Conclusion: This newly generated AA98 VH/L antibody displays a therapeutic potential for tumor and other angiogenesis disorders, as well as providing a new strategy for antibody engineering for clinical applications.
Footnotes
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↵* Present address: Memorial Sloan-Kettering Cancer Center, New York, NY, U.S.A.
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↵** Present address: Research Division of the Puget Sound Blood Center, Seattle, WA, U.S.A.
- Received May 28, 2007.
- Revision received October 12, 2007.
- Accepted October 22, 2007.
- Copyright© 2007 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved





