Immunization with WT1-derived peptides by tattooing inhibits the growth of TRAMP-C2 prostate tumor in mice
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
22735806
DOI
10.1097/cji.0b013e3182618381
PII: 00002371-201207000-00004
Knihovny.cz E-resources
- MeSH
- Adjuvants, Immunologic MeSH
- Azacitidine analogs & derivatives pharmacology therapeutic use MeSH
- Decitabine MeSH
- Injections, Intradermal MeSH
- Antibodies, Monoclonal immunology MeSH
- Mice, Inbred BALB C MeSH
- Mice MeSH
- Cell Line, Tumor MeSH
- Prostatic Neoplasms therapy MeSH
- Poly I-C pharmacology therapeutic use MeSH
- WT1 Proteins administration & dosage immunology MeSH
- Antineoplastic Agents pharmacology therapeutic use MeSH
- Cancer Vaccines administration & dosage MeSH
- Vaccines, Subunit administration & dosage MeSH
- Tattooing MeSH
- Transforming Growth Factor beta antagonists & inhibitors immunology MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Adjuvants, Immunologic MeSH
- Azacitidine MeSH
- Decitabine MeSH
- Antibodies, Monoclonal MeSH
- Poly I-C MeSH
- WT1 Proteins MeSH
- Antineoplastic Agents MeSH
- Cancer Vaccines MeSH
- Vaccines, Subunit MeSH
- Transforming Growth Factor beta MeSH
The expression of the transcription factor encoded by the Wilms tumor gene 1 (WT1) is associated with a variety of human cancers. WT1 protein has been reported to serve as a target antigen for tumor-specific immune responses. We observed that the immunization of mice with peptide vaccines derived from WT1 in a mixture with the CpG adjuvant (ODN 1826) by tattoo administration was superior to subcutaneous delivery of the peptides in combination with CpG formulated with the mineral oil adjuvant or a DNA vaccine or a recombinant vaccinia virus vaccine expressing the truncated WT1 protein. Tattooing with the WT1122-140 and WT1126-134 peptide elicited the response of WT1-specific interferon-γ-producing T cells. Peptide vaccine administered with a tattoo device had an antitumor effect on the growth of the prostate tumor cell line TRAMP-C2, provided that the transforming growth factor-β produced by tumor cells was neutralized by anti-TGFβ monoclonal antibody. The treatment of the tumor-bearing mice with 5-azadeoxycytidine or poly IC did not work in synergy with the peptide vaccine.
References provided by Crossref.org