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Immunological features of T cells induced by human telomerase reverse transcriptase-derived peptides in patients with hepatocellular carcinoma.

Authors :
Mizukoshi E
Nakagawa H
Kitahara M
Yamashita T
Arai K
Sunagozaka H
Fushimi K
Kobayashi E
Kishi H
Muraguchi A
Kaneko S
Source :
Cancer letters [Cancer Lett] 2015 Aug 10; Vol. 364 (2), pp. 98-105. Date of Electronic Publication: 2015 May 14.
Publication Year :
2015

Abstract

Human telomerase reverse transcriptase (hTERT) is a catalytic enzyme required for telomere elongation. In this study, we investigated the safety and immunogenicity of an hTERT-derived peptide (hTERT461) as a vaccine and characterized the hTERT-specific T cell responses induced. Fourteen hepatocellular carcinoma (HCC) patients were enrolled in the study. The hTERT-derived peptide was emulsified in incomplete Freund's adjuvant and administered via subcutaneous immunization three times biweekly. The maximum toxicity observed was grade 2 according to the common terminology criteria and mainly consisted of skin reactions at the site of vaccination. The vaccination induced hTERT-specific immunity in 71.4% of patients and 57.1% of patients administered with hTERT461 peptide-specific T cells could prevent HCC recurrence after vaccination. In phenotypic analysis, the post-vaccinated increase in hTERT-specific T cells was due to an increase in cells with the effector memory phenotype, with the potential to produce multiple cytokines. Seven hTERT-specific T cell receptors were obtained from the vaccinated patients, showing their cytotoxic activities to hTERT-derived peptide-bearing cells. In conclusion, the safety and effects of immune boosting by hTERT461 peptide have shown the potential of the peptide to provide clinical benefits in HCC patients.<br /> (Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1872-7980
Volume :
364
Issue :
2
Database :
MEDLINE
Journal :
Cancer letters
Publication Type :
Academic Journal
Accession number :
25982205
Full Text :
https://doi.org/10.1016/j.canlet.2015.04.031