Production and functional characterization of two mouse/human chimeric antibodies with specificity for the tumor-associated Tn-antigen

ANTIGENOS

INMUNOLOGIA

NEOPLASMAS

BIBLIOGRAFIA NACIONAL QUIMICA

2000

In this work, we have constructed two functional mouse/human chimeric antibodies (IgMκ and IgG1κ isotypes) by inserting genomic DNA fragments encoding VH and Vκ variable regions of the murine monoclonal antibody IgMκ-83D4 into mammalian expression vectors containing human μ, γ1, and κ constant exons, and by transfecting them into the nonsecreting mouse myeloma X-63 cell line. In previous works, we have demonstrated that 83D4 murine mAb reacts with Tn determinant (GalNAcα-O-Ser/Thr) expressed in 90% of breast, ovary, and colon carcinomas. Both expressed chimeric antibodies were purified from the transfected cell line supernatant by affinity chromatography, and their reactivities against Tn antigen were confirmed by ELISA on asialo ovine submaxilar mucin and immunofluorescence studies on MCF-7 breast carcinoma cell line. We have demonstrated by gel filtration chromatography, that the principal secreted forms were monomers for IgG1κ and pentamers for IgMκ. The binding affinities of these chimeric antibodies against synthetic Tn glycopeptides, were evaluated by surface plasmon resonance showing an affinity constant similar to that of 83D4 native antibody for IgMκ and a lower affinity constant for IgG1κ chimeric antibody. On the other hand, the replacement of mouse C regions with human C regions confers both chimeric antibodies the ability to activate human complement. These mouse/human chimeric antibodies should be much less immunogenic and could play an important role in the lysis of tumor cell expressing Tn-antigen. Therefore, these anti-Tn chimeric antibodies could be considered as potential tools for human in vivo studies.

Hybridoma v. 19, , 2000. -- p. 229-239

Mary Ann Liebert, Inc.

2000

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DOI:10.1089/02724570050109620.