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Clinical Cancer Research Vol. 8, 1720-1730, June 2002
© 2002 American Association for Cancer Research

Experimental Therapeutics, Preclinical Pharmacology

Targeting Multiple Her-2 Epitopes with Monoclonal Antibodies Results in Improved Antigrowth Activity of a Human Breast Cancer Cell Line in Vitro and in Vivo1

Camelia I. Spiridon, Maria-Ana Ghetie, Jonathan Uhr, Radu Marches, Jia-Ling Li, Guo-Liang Shen and Ellen S. Vitetta2

Cancer Immunobiology Center, U. T. Southwestern Medical School, Dallas, Texas 75390-8576

Her-2 (p185erbB-2) is a transmembrane tyrosine kinase receptor, which is encoded by the Her-2/neu proto-oncogene. Her-2 is overexpressed on 30% of highly malignant breast cancers. Monoclonal antibodies (MAbs) against Her-2 inhibit the growth of Her-2-overexpressing tumor cells and this occurs by a variety of mechanisms. One such MAb, Herceptin (Trastuzumab), has been approved for human use. We have generated a panel of murine anti-Her-2 MAbs against nine different epitopes on the extracellular domain of Her-2 and have evaluated the antitumor activity of three of these MAbs alone and in combination, both in vitro and in vivo. We found that MAbs (against different epitopes) make a highly effective mixture, which was more effective than the individual MAbs in treating s.c. tumor nodules of BT474 cells in SCID mice. In vitro, the MAb mixture was also more effective than the single MAbs in inducing antibody-dependent cellular cytotoxicity and complement-dependent cytotoxicity, inhibiting cell growth and inducing apoptosis, and inhibiting the secretion of vascular endothelial growth factor. Taken together, these activities might explain the superior performance of the MAb mixture in vivo.




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Copyright © 2002 by the American Association for Cancer Research.