| Literature DB >> 11597390 |
P Correale1, M G Cusi, M Sabatino, L Micheli, D Pozzessere, C Nencini, P E Valensin, R Petrioli, G Giorgi, R Zurbriggen, R Gluck, G Francini.
Abstract
We investigated influenza virosomes as a TAA-gene delivery system for use in TAA-directed anti-cancer vaccine therapy. An engineered plasmid (GC90) expressing the parathyroid hormone-related peptide (PTH-rP), a protein secreted by prostate and lung carcinoma cells, was included in influenza virosomes (GC90V). The ability of GC90V to elicit a PTH-rP-specific cytotoxic T cell (CTL) response was demonstrated in BALB/c mice immunised with intranasal (i.n.) GC90V+/-adjuvant subcutaneous (s.c.) interleukin-2 (IL-2). A PTH-rP-specific CTL response with antitumour activity was also demonstrated in human peripheral blood mononuclear cells (PBMC) stimulated in vitro with GC90V infected autologous dendritic cells (DC). These results provide a rationale for investigating GC90V in clinical trials of anticancer vaccine therapy.Entities:
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Year: 2001 PMID: 11597390 DOI: 10.1016/s0959-8049(01)00241-6
Source DB: PubMed Journal: Eur J Cancer ISSN: 0959-8049 Impact factor: 9.162