| Literature DB >> 20600515 |
Laïla-Aïcha Hanafi1, Marilène Bolduc, Marie-Eve Laliberté Gagné, Florent Dufour, Yves Langelier, Mohammed-Rachid Boulassel, Jean-Pierre Routy, Denis Leclerc, Réjean Lapointe.
Abstract
Chimeric VLPs made of papaya mosaic virus (PapMV) trigger a CTL response through antigenic presentation of epitopes on MHC class I. Here, a chimeric VLP composed of malva mosaic virus (MaMV) was shown to share similar properties. We demonstrated the capacity of both VLPs to enter human APCs. The chimeric constructions were cross-presented in CD40-activated B lymphocytes leading to in vitro expansion of antigen-specific T lymphocytes. We showed that high concentrations of chimeric MaMV induced cell death, suggesting that some modifications can trigger collateral effects in vitro. Results suggest that potexvirus VLPs are an attractive vaccine platform for inducing a CTL response. Copyright 2010 Elsevier Ltd. All rights reserved.Entities:
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Year: 2010 PMID: 20600515 DOI: 10.1016/j.vaccine.2010.06.024
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641