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Nat Biotechnol ; 24(2): 205-9, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16444269

ABSTRACT

Cancer cells differ from normal cells in their response to chemotherapy. We exploited this dissimilarity by identifying and targeting tumor-specific, cell-surface proteins whose expression is induced by the chemotherapeutic irinotecan (CPT-11; Camptosar). A cytotoxin-armed antibody reactive with one of these drug-induced surface proteins, the LY6D/E48 antigen, originally identified as the target of a monoclonal antibody reactive with squamous cell carcinomas, caused complete regression of colorectal tumor xenografts in mice treated with CPT-11, whereas either agent alone was less effective. These results suggest that a positive therapeutic index may be generated for other drug combinations by immunotherapeutic targeting of chemotherapy-induced antigens.


Subject(s)
Antibodies, Monoclonal/therapeutic use , Antigens, Neoplasm/immunology , Camptothecin/analogs & derivatives , Carcinoma, Squamous Cell/drug therapy , Carcinoma, Squamous Cell/immunology , Drug Delivery Systems/methods , Immunotherapy/methods , Animals , Antibodies, Monoclonal/immunology , Antineoplastic Agents/administration & dosage , Base Sequence , Camptothecin/administration & dosage , Camptothecin/immunology , Cell Line, Tumor , Female , Humans , Irinotecan , Membrane Proteins/immunology , Mice , Mice, Nude , Molecular Sequence Data , Treatment Outcome
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