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Protein Engineering vol. 1 no. 6 pp. 499-505, 1987
© 1987 Oxford University Press


OTHER

Expression in COS cells of a mouse—human chimaeric B72.3 antibody

Nigel Whittle*, John Adair, Chris Lloyd, Liz Jenkins, Joan Devine, Jeffrey Schlom1, Andrew Raubitschek1, David Colcher1 and Mark Bodmer

1Laboratory of Tumor Immunology and Biology, National Cancer Institute NIH, Bethesda, MD 20205, USA Department of Molecular Immunology, Celltech Limited 216-222 Bath Road, Slough SLI 4EN, UK

*To whom reprint requests should be sent

B72.3 is a mouse hybndoma cell-line secreting an IgG1 antibody which recognises an epitope on a tumour-associated antigen, TAG-72. This high molecular weight mucin-like molecule is found on a variety of human neoplasms, including colon, breast and ovarian carcinomas. Chimaeric Immunoglobulin genes with the B72.3 specificity have been constructed by joining the mouse variable regions from cDNA clones to human genomic constant regions using recombinant DNA techniques. The chimaeric heavy and light chain Immunoglobulin genes were placed under the control of a strong viral promoter, and co-transfected into COS-1 cells. SDS–PAGE analysis of the 35S-labelled products demonstrated that the transiently expressed antibodies were correctly synthesised and assembled. The specific binding characteristics of the parent B72.3 antibody were retained by the chimaeric antibody in an antigen-based ELISA. This system gave sufficiently high transient expression of the chlmaerlc antibody molecules to allow rapid physical and Immunological characterisation of the engineered gene products.

Keywords: chimaeric antibody/cancer immunotherapy/DNA transfection/transient expression

Received October 8, 1987; revised December 8, 1987;
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