Cancer Research CTRC-AACR San Antonio Breast Cancer Symposium  Tumor Immunology: New Perspectives
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[Cancer Research 49, 4852-4858, September 1, 1989]
© 1989 American Association for Cancer Research

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Antigenic Sites in Carcinoembryonic Antigen1

Sten Hammarstrom, John E. Shively2, Raymond J. Paxton, Barbara G. Beatty, Åke Larsson, Rahul Ghosh, Ole Bormer, Franz Buchegger, Jean-Pierre Mach, Pierre Burtin, P. Seguin, Bruno Darbouret, F. Degorce, J. Sertour, J. P. Jolu, Abraham Fuks, Holger Kalthoff, Wolff Schmiegel, Rudiger Arndt, Gunter Kloppel, Sabine von Kleist, Fritz Grunert, Klaus Schwarz, Yuji Matsuoka, Masahide Kuroki, Christoph Wagener, Teddy Weber, Akira Yachi, Kohzoh Imai, Noriyuki Hishikawa and Masayuki Tsujisaki

University of Umeå, Umeå [S. H.]; Beckman Research Institute, City of Hope, Duarte [J. E. S., R. J. P., B. G. B.]; University of Stockholm, Stockholm [A. L., R. G.]; The Norwegian Radium Hospital, Oslo [O. B.]; University of Lausanne [F. B., J-P. M.]; Centre National De La Recherche Scientifique, Villejuif [P. B.]; Oris Industrie, Bagnols sur Ceze Cedex [P. S., B. D., F. D., J. S., J. P. J.]; McGill University, Montreal [A. F.]; University Hospital, Hamburg [H. K., W. S., R. A., G. K.]; Albert-Ludwigs University, Freiburg [S. V. K., F. G., K. S.]; Fukuoka University [Y. M., M. K.]; University of Technology, Aachen [C. W.]; Medix Biochemica, Helsinki [T. W.]; Sapporo Medical School, Sapporo [A. Y., K. I., N. H., M. T.]

The epitope reactivities of 52 well-characterized monoclonal antibodies (Mabs) against carcinoembryonic antigen from 11 different research groups were studied using competitive solid-phase immunoassays. About 60% of all possible combinations of Mabs as inhibitors and as the primary binding antibody were investigated. The inhibition data were analyzed by a specially developed computer program "EPITOPES" which measures concordance and discordance in inhibition patterns between Mabs. The analysis showed that 43 of the 52 Mabs (83%) could be classified into one of five essentially noninteracting epitope groups (GOLD 1–5) containing between four and 15 Mabs each. The epitopes recognized by the Mabs belonging to groups 1 to 5 were peptide in nature. With one or two possible exceptions non-classifiable Mabs were either directed against carbohydrate epitopes (4 Mabs) or were inactive in the tests used. Within epitope groups GOLD 1, 4, and 5 two partially overlapping subgroups were distinguished. Mabs with a high degree of carcinoembryonic antigen specificity generally belonged to epitope groups GOLD 1 and 3.

1 This study represents the work of an international workshop on the epitope reactivity of monoclonal antibodies against carcinoembryonic antigen.

2 To whom requests for reprints should be addressed, at Beckman Research Institute of the City of Hope, Division of Immunology, 1450 East Duarte Road, Duarte, CA 91010.

Received 8/24/88. Revised 4/12/89. Accepted 5/ 2/89.




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Copyright © 1989 by the American Association for Cancer Research.