| Literature DB >> 12239302 |
Yu-Zhang Wu1, Jian-Ping Zhao, Ying Wan, Zheng-Cai Jia, Wei Zhou, Jiang Bian, Bing Ni, Li-Yun Zou, Yan Tang.
Abstract
CD8(+) cytotoxic T lymphocytes (CTLs) are now recognized as important mediators of immunity against intracellular pathogens, including human immunodeficiency virus and tumors. How to efficiently evoke antigen-specific CTL responses in vivo has become a crucial problem in the development of modern vaccines. Here, we developed a completely novel CTL vaccine-mimovirus, which is a kind of virus-size particulate antigen delivery system. It was formed by the self-assembly of a cationic peptide containing 18 lysines and a CTL-epitope peptide of HBsAg(28-39), with a plasmid encoding mouse interleukin-12 (IL-12) through electrostatic interactions. We examined the formation of mimovirus by DNA retardation assay, DNase I protection assay, and transmission electron microscopy and demonstrated that mimovirus could efficiently transfer the plasmid encoding IL-12 into mammalian cells such as P815 cells in vitro. Furthermore, it was proved that mimovirus could induce an HBsAg(28-39)-specific CTL response in vivo. Considering its effectiveness, flexibility, and defined composition, mimovirus is potentially a novel system for vaccination against intracellular pathogens and tumors.Entities:
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Year: 2002 PMID: 12239302 PMCID: PMC136564 DOI: 10.1128/jvi.76.20.10264-10269.2002
Source DB: PubMed Journal: J Virol ISSN: 0022-538X Impact factor: 5.103