Many mechanisms have been proposed for the positive effects of monoclonal antibodies in cancer therapy. New data indicate that both the variable, antigen-binding region of an antibody and the Fc region are capable of influencing anti-cancer immunity (pages 443–446).
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References
Kohler, G. & Milstein, C. Continuous cultures of fused cells secreting antibody of predefined specificity. Nature 256, 495–497 (1975).
Clynes, R.A., Towers, T.L., Persta, L.G., & Ravetch, J.V. Inhibitory Fc receptors modulate in vivo cytotoxicity against tumor targets. Nature Med. 6, 443– 446 (2000).
Masui, H. et al. Growth inhibition of human tumor cells in athymic mice by anti-epidermal growth factor receptor monoclonal antibodies. Cancer Res. 44, 1002–1007 (1984).
Drebin, J.A., Link, V.C., Stern, D.F., Weinberg, R.A. & Greene, M.I. Downregulation of an oncogene protein product and reversion of the transformed phenotype by monoclonal antibodies. Cell 41, 697–706 ( 1985).
Waldmann, T.A. The multichain interleukin-2 receptor: from the gene to the bedside. Harvey Lect. 82, 1–17 ( 1986).
Dinney, C.P. et al. Therapy of human transitional cell carcinoma of the bladder by oral administration of the epidermal growth factor receptor protein tyrosine kinase inhibitor 4,5-dianilinophthalimide. Clin. Cancer Res. 3, 161–168 (1997).
Park, B.W. et al. Rationally designed anti-HER2/neu peptide mimetic disables P185HER2/ neu tyrosine kinases in vitro and in vivo. Nature Biotechnol. 18, 194–198 (2000).
Vuist, W.M. et al. Lymphoma regression induced by monoclonal anti-idiotypic antibodies correlates with their ability to induce Ig signal transduction and is not prevented by tumor expression of high levels of Bcl-2 protein. Blood 83, 899–906 ( 1994).
Vadhan-Raj, S. et al. Phase I trial of a mouse monoclonal antibody against GD3 ganglioside in patients with melanoma: induction of inflammatory responses at tumor sites . J. Clin. Oncol. 6, 1636– 1648 (1988).
Clynes, R., Takechi, Y., Moroi, Y., Houghton, A., & Ravetch, J.V. Fc receptors are required in passive and active immunity to melanoma. Proc. Natl. Acad. Sci. USA 95, 652–656 (1998).
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Houghton, A., Scheinberg, D. Monoclonal antibody therapies–a ‘constant’ threat to cancer. Nat Med 6, 373–374 (2000). https://doi.org/10.1038/74621
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DOI: https://doi.org/10.1038/74621
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