Abstract
A new human, compact antibody was engineered by fusion of a human, antitumour ErbB2-directed scFv with a human IgG1 Fc domain. Overexpression of the ErbB2 receptor is related to tumour aggressiveness and poor prognosis. This new immunoagent meets all criteria for a potential anticancer drug: it is human, hence poorly or not immunogenic; it binds selectively and with high affinity to target cells, on which it exerts an effective and selective antiproliferative action, including both antibody-dependent and complement-dependent cytotoxicity; it effectively inhibits tumour growth in vivo. Its compact molecular size should provide for an efficient tissue penetration, yet suitable to a prolonged serum half-life.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antibodies / pharmacology*
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Antibodies, Monoclonal / pharmacology*
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Antibodies, Monoclonal / therapeutic use
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Antibodies, Monoclonal, Humanized
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Antineoplastic Agents / pharmacology*
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Base Sequence
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CHO Cells
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Cell Division / drug effects
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Cell Line, Tumor
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Cricetinae
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DNA Primers
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Female
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Humans
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Mice
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Mice, Inbred BALB C
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Neoplasms, Experimental / drug therapy
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Neoplasms, Experimental / pathology
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Polymerase Chain Reaction
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Receptor, ErbB-2 / genetics
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Receptor, ErbB-2 / immunology*
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Recombinant Fusion Proteins / pharmacology
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Trastuzumab
Substances
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Antibodies
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Antibodies, Monoclonal
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Antibodies, Monoclonal, Humanized
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Antineoplastic Agents
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DNA Primers
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Recombinant Fusion Proteins
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Receptor, ErbB-2
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Trastuzumab