A Chemically Induced Vaccine Strategy for Prostate Cancer

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 i...

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Veröffentlicht in:ACS chemical biology 2011-11, Vol.6 (11), p.1223-1231
Hauptverfasser: Dubrovska, Anna, Kim, Chanhyuk, Elliott, Jimmy, Shen, Weijun, Kuo, Tun-Hsun, Koo, Dong-In, Li, Chun, Tuntland, Tove, Chang, Jonathan, Groessl, Todd, Wu, Xu, Gorney, Vanessa, Ramirez-Montagut, Teresa, Spiegel, David A, Cho, Charles Y, Schultz, Peter G
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Sprache:eng
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Zusammenfassung: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.
ISSN:1554-8929
1554-8937
DOI:10.1021/cb200222s