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[Cancer Research 46, 3848-3854, August 1, 1986]
© 1986 American Association for Cancer Research

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Modes of Binding and Internalization of Monoclonal Antibodies to Human Melanoma Cell Lines1

Siegfried Matzku2, Eva-Bettina Bröcker, Josef Brüggen, Wolfgang G. Dippold and Wolfgang Tilgen

German Cancer Research Center, Institute of Nuclear Medicine, D-6900 Heidelberg [S. M.]; Department of Experimental Dermatology, Westfälische Wilhelms-Universität, D-4400 Münster, [E-B. B., J. B.]; I. Med. Klinik und Poliklinik, Johannes Gutenberg-Universität, D-6500 Mainz [W. G. D.]; and Universitäts-Hautklinik, D-6900 Heidelberg [W. T.], Germany

The process of monoclonal antibody (MAb) binding to tumor cells is greatly influenced by the biology of the respective antigen. This was concluded from an analysis of binding and release of MAbs and MAb fragments to melanoma cells at different concentration levels and different temperatures. With an antigen known to be stably expressed at the cell surface (i.e., Mr 97,000 protein) rapid binding of MAbs was observed at both 0°C and 37°C, and this was reversed by treatment with isoosmolar acid buffer. With another group of antigens, MAb binding increased continuously up to considerable levels at 37°C, but not at 0°C. Concomitantly, the portion of radioactive MAb not desorbable by acid buffer treatment increased, pointing to temperature-dependent internalization. With still another group of (glycolipid) antigens, the highest MAb binding was obtained with fixed cells at 0°C. In this situation MAb release was particularly rapid, thus pointing to a shedding process.

1 This work was supported by the Sonderforschungsbereich 136 "Krebsforschung," Deutsche Forschungsgemeinschaft.

2 To whom requests for reprints should be addressed, at Pf. 101949, D-6900 Heidelberg, Germany.

Received 7/ 2/85. Revised 2/12/86. Accepted 4/30/86.




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[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1986 by the American Association for Cancer Research.