BMC Immunology | |
Chitosan gel vaccine protects against tumour growth in an intracaecal mouse model of cancer by modulating systemic immune responses | |
Research Article | |
Roslyn A. Kemp1  Georgia M. Bell1  Andrew J. Highton1  Adam Girardin1  Sarah M. Hook2  | |
[1] Department of Microbiology and Immunology, Otago School of Medical Sciences, University of Otago, PO Box 56, 9054, Dunedin, New Zealand;School of Pharmacy, University of Otago, Dunedin, New Zealand; | |
关键词: Colon cancer; IFN-γ; T cells; Vaccination; Tumour; Caecum; | |
DOI : 10.1186/s12865-016-0178-4 | |
received in 2016-07-02, accepted in 2016-10-13, 发布年份 2016 | |
来源: Springer | |
【 摘 要 】
BackgroundVaccination generating a robust memory population of CD8+ T cells may provide protection against cancer. However, immune therapies for cancer are influenced by the local tumour immune microenvironment. An infiltrate of T cells into tumours of people with colorectal cancer has proven to be a significant indicator of good prognosis.MethodsWe used an intracaecal mouse model of cancer to determine whether a protective immune response against a mucosal gut tumour could be generated using a systemic intervention. We investigated the generation of murine memory CD8+ T cells using a sustained antigen release vaccine vehicle (chitosan gel; Gel + OVA) containing the model antigen ovalbumin, chitosan gel alone (Gel) or conventional dendritic cell vaccination (DC + OVA) using the same protein antigen.ResultsFollowing vaccination with Gel + OVA, CD8+ T cell memory populations specific for ovalbumin protein were detected. Only vaccination with Gel + OVA gave decreased tumour burden compared to unvaccinated or DC + OVA-vaccinated mice in the intracaecal cancer challenge model.ConclusionThese results indicate that subcutaneous vaccination with Gel + OVA generates a population of functional CD8+ memory T cells in lymphoid tissue able to protect against intracaecal tumour challenge. Vaccination with chitosan gel may be valuable in anti-cancer treatment at both peripheral and mucosal sites.
【 授权许可】
CC BY
© The Author(s). 2016
【 预 览 】
Files | Size | Format | View |
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RO202311108214146ZK.pdf | 969KB | download |
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