Abstract
Two immunotoxins were constructed by chemically coupling the monoclonal antibody C242 to Pseudomonas exotoxin A (PE) or a modified form, NlysPE40, that lacks the cell binding domain of PE. Monoclonal antibody C242 recognizes a specific sialylated carbohydrate epitope on a high molecular weight membrane glycoprotein present on cells of human colon, pancreatic, and cervical cancers. C242-PE and C242-NlysPE40 were very cytotoxic for cells expressing this antigen with 50% inhibition of protein synthesis occurring on Colo205 cells at 0.2 ng/ml (0.9 pM) for C242-PE and 6.0 ng/ml (31 pM) for C242-NlysPE40. The two immunotoxins also exhibited a strong antitumor effect on a human colon cancer xenograft grown in nude mice. The specificity and potency of these two C242 immunotoxins warrant their further development for the treatment of cancer.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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ADP Ribose Transferases*
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Adenocarcinoma / therapy
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Amino Acid Sequence
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Animals
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Antibodies, Monoclonal / administration & dosage*
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Antibodies, Neoplasm / administration & dosage*
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Antibody Affinity
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Antigens, Tumor-Associated, Carbohydrate / immunology*
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Bacterial Toxins*
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Base Sequence
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Colonic Neoplasms / therapy*
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Exotoxins / administration & dosage*
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Exotoxins / toxicity
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Humans
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Immunotherapy
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Immunotoxins / chemistry*
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In Vitro Techniques
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Mice
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Mice, Nude
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Molecular Sequence Data
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Neoplasm Proteins / biosynthesis
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Neoplasm Transplantation
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Oligodeoxyribonucleotides / chemistry
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Pseudomonas aeruginosa Exotoxin A
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Recombinant Fusion Proteins
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Transplantation, Heterologous
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Tumor Cells, Cultured
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Virulence Factors*
Substances
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Antibodies, Monoclonal
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Antibodies, Neoplasm
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Antigens, Tumor-Associated, Carbohydrate
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Bacterial Toxins
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Exotoxins
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Immunotoxins
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Neoplasm Proteins
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Oligodeoxyribonucleotides
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Recombinant Fusion Proteins
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Virulence Factors
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ADP Ribose Transferases