Intracellular Targeting with Low pH-triggered Bispecific Antibodies

• Published in: The Journal of biological chemistry 1997-10, Vol.272 (44), p.27623-27628
• Main Authors: Raso, Vic, Brown, Michelle, McGrath, John
• Format: Article
• Language: English
• Subjects: Antibodies, Bispecific - immunology; Binding Sites, Antibody; Diphtheria Toxin - immunology; Diphtheria Toxin - metabolism; Endosomes - metabolism; Humans; Hydrogen-Ion Concentration; Iodine Radioisotopes; Tumor Cells, Cultured
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.272.44.27623

Bispecific antibodies were designed to deliver a reversibly bound ligand into target cells and then spontaneously release it upon passage into acidified vesicles. These reagents were assembled by coupling monoclonal antibodies that recognize acid-sensitive epitopes on diphtheria toxin to cell type-specific monoclonal antibodies. The dual binding capacity of the bispecific antibodies was confirmed by delivery of125I-diphtheria toxin to target molecules present on intact cells. Bispecific antibodies directed against transferrin receptors on human cells were loaded with toxin and tested for cytotoxicity. The mutant diphtheria toxins CRM107 and CRM45 were used since their inability to bind cell receptors renders them ordinarily nontoxic. Their full cytotoxic potential, however, was restored via bispecific antibody-mediated delivery and release within low pH intracellular vesicles. Cytotoxicity was shown to be specific by blocking receptor sites and to be acidification-dependent by protection using NH4Cl to raise endosomal pH. Kinetics for inhibition of cellular protein synthesis was identical for native diphtheria toxin and the bispecific antibody·CRM107 combination. The rate of inhibition (t1/2 = 20 min) indicated that release of CRM107 from the antibody combining site was fast, and its toxic action was unimpeded by this delivery mechanism.