CHARACTERIZATION OF A HUMANIZED BISPECIFIC MONOCLONAL-ANTIBODY FOR CANCER-THERAPY

被引:13
作者
BRUYNCK, A [1 ]
SEEMANN, G [1 ]
BOSSLET, K [1 ]
机构
[1] BEHRINGWERKE AG, RES LABS, POB 1140, W-3550 MARBURG, GERMANY
关键词
D O I
10.1038/bjc.1993.84
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A humanised bispecific monoclonal antibody (bsMAb) with binding specificity for carcinoembryonic antigen (CEA) on one arm and a radiolabelled chelate (DTPA-Y-90) on the other arm was generated by consecutively transfecting the humanised genes of an anti-CEA MAb and the chimerised genes of an anti-chelate MAb into eucaryotic BHK cells using the calcium-phosphate coprecipitation technique. The antibodies secreted were of IgG3 isotype with a shortened hinge region (DELTA gamma 3) and light chains. Double transfectomas were screened for the secretion of bsMAbs using a double determinant enzyme-linked immunosorbent assay (ELISA) based on solid phase attached HSA-benzyl-DTPA and an anti-idiotypic MAb selective for the CEA-specific arm. After purification on two immunoaffinity chromatography columns, the humanised bsMAbs were characterised by SDS-PAGE and a quantitative binding assay in antigen excess. The purification procedure resulted in 95% reactive bispecific MAb. This humanised bsMAb may be employed in two phase radioimmunotherapy, binding to the tumour via the anti-CEA arm and localising a radiolabelled chelate with the other arm, without inducing a strong immune response observed sometimes with murine MAbs.
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页码:436 / 440
页数:5
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