Volume 11 Supplement 1
HTLV-1 Tax peptide-carrying polyion complex nanoparticles induce potent cellular immunity in mice
© Uto et al; licensee BioMed Central Ltd. 2014
Published: 7 January 2014
Development of safe and effective vaccines is important for controlling a variety of infectious diseases, including retroviral infections. The induction of cytotoxic T lymphocytes (CTLs) is a promising strategy for elimination of infected cells. Polyion complex (PIC) nanoparticles have been created using anionic biodegradable poly(γ-glutamic acid) (γ-PGA) and cationic protamine. Amphiphilic graft copolymers, consisting of γ-PGA and l-phenylalanine (l-Phe) hydrophobic side chain, were synthesized by grafting l-Phe to γ-PGA. The PIC nanoparticles were prepared by mixing the graft copolymers with protamine in phosphate buffered saline. In this study, antigen peptide-carrying PIC nanoparticles were examined for their effect on the induction of antigen-specific cellular immunity in mice. The antigen-specific CTL response was evaluated by intracellular cytokine staining and IFN-γ ELISPOT assay. The immunization with PIC nanoparticles carrying HTLV-1 Tax peptide could induce the expansion of Tax-specific CD8+ T cells. In contrast, no such induction of the antigen-specific CD8+ T cells was observed, when mice were immunized with the peptide alone or peptide plus an aluminum adjuvant. These results suggest that the Tax peptide-carrying PIC nanoparticles are capable of inducing cellular immune responses and may have potential as an effective vaccine adjuvant for anti-HTLV-1 vaccines.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.