Back to Search
Start Over
A DNA telomerase vaccine for canine cancer immunotherapy
- Source :
- Oncotarget
- Publication Year :
- 2019
- Publisher :
- Impact Journals, LLC, 2019.
-
Abstract
- Telomerase reverse transcriptase (TERT) is highly expressed in more than 90% of canine cancer cells and low to absent in normal cells. Given that immune tolerance to telomerase is easily broken both naturally and experimentally, telomerase is an attractive tumor associated antigen for cancer immunotherapy. Indeed, therapeutic trials using human telomerase peptides have been performed. We have developed an immunogenic yet catalytically inactive human telomerase DNA construct that is in clinical trials with patients presenting solid tumors. Paralleling this human construct, we have developed a canine telomerase DNA vaccine, called pDUV5. When administered intradermally to mice combined with electrogene transfer, pDUV5 induced canine TERT specific cytotoxic T-cells as measured by IFN-γ ELISpot assay. Intradermal vaccination of healthy dogs with 400 μg of pDUV5 generated strong, broad and long lasting TERT specific cellular immune responses. In vitro immunization with cTERT peptides revealed the maintenance of cTERT specific T-cells in PBMCs from tumor bearing dogs showing that this repertoire was not depleted. This study highlights the potential of pDUV5 as a cancer vaccine and supports its evaluation for the treatment of spontaneous canine tumors.
- Subjects :
- DNA vaccine
0301 basic medicine
Telomerase
medicine.medical_treatment
DNA vaccination
03 medical and health sciences
0302 clinical medicine
Cancer immunotherapy
medicine
cancer
Telomerase reverse transcriptase
business.industry
Electro-Gene-Transfer
ELISPOT
Cancer
Immunotherapy
medicine.disease
030104 developmental biology
Oncology
canine TERT
030220 oncology & carcinogenesis
Cancer research
immunotherapy
Cancer vaccine
business
Research Paper
Subjects
Details
- ISSN :
- 19492553
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- Oncotarget
- Accession number :
- edsair.doi.dedup.....e3dec7a4e31082f5eed8f57e05e89588