An artificial PAP gene breaks self-tolerance and promotes tumor regression in the TRAMP model for prostate carcinoma - Abstract

Division of Immunology, Department of Biology, University of Constance, Constance, Germany.

 

Prostate cancer (PCa) is the most commonly diagnosed type of cancer in men in western industrialized countries. As a public health burden, the need for the invention of new cost-saving PCa immunotherapies is apparent. In this study, we present a DNA vaccine encoding for the prostate-specific antigen prostatic acid phosphatase (PAP) linked to the J-domain and the SV40 enhancer sequence. The PAP DNA vaccine induced a strong PAP-specific cellular immune response after electroporation (EP)-based delivery in C57BL/6 mice. Splenocytes from mice immunized with PAP recognized the naturally processed PAP epitopes, indicating that vaccination with the PAP-J gene broke its self-tolerance against PAP. Remarkably, DNA vaccination with PAP-J inhibited tumor growth in the Transgenic Adenocarcinoma of the Mouse Prostate (TRAMP) mouse model that closely resembled human PCa. Therefore, this study highlights a novel cancer immunotherapy approach with the potential to control PCa in clinical settings.

Written by:
Spies E, Reichardt W, Alvarez G, Groettrup M, Ohlschläger P.   Are you the author?

Reference: Mol Ther. 2011 Nov 15. Epub ahead of print.
doi: 10.1038/mt.2011.241

PubMed Abstract
PMID: 22086231

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