A Chemically Induced Vaccine Strategy for Prostate Cancer
Citations Over TimeTop 10% of 2011 papers
Abstract
Here we report the design and evaluation of a bifunctional, small molecule switch that induces a targeted immune response against tumors in vivo. A high affinity ligand for prostate specific membrane antigen (PSMA) was conjugated to a hapten that binds dinitrophenyl (DNP)-specific antibodies. When introduced into hu-PBL-NOD/SCID mice previously immunized with a KLH-DNP immunogen, this conjugate induced a targeted antibody-dependent cellular cytotoxicity (ADCC) response to PSMA-expressing tumor cells in a mouse xenograft model. The ability to create a small molecule inducible antibody response against self-antigens using endogenous non-autoreactive antibodies may provide advantages over the autologous immune response generated by conventional vaccines in certain therapeutic settings.
Related Papers
- → Antibody production: Low dose immunogen vs. low incorporation hapten using salmeterol as a model(2008)23 cited
- → Development of a Cross-Reactive Monoclonal Antibody to Sulfonamide Antibiotics: Evidence for Structural Conformation-Selective Hapten Recognition(1999)47 cited
- → Development of a Panel of Immunoassays for Monitoring DDT, Its Metabolites, and Analogues in Food and Environmental Matrices(1998)27 cited
- → Heteroclitic cells in anti-hapten systems: Some studies at the cellular and serum level(1972)13 cited
- → Production of Methotrexate antiserum in rabbits: the significance of immunogen solubility, hapten content, and mode of administration on the antibody response(1977)4 cited