| Literature DB >> 32497512 |
Thomas D Norton1, Takuya Tada2, Rebecca Leibowitz3, Verena van der Heide4, Dirk Homann4, Nathaniel R Landau5.
Abstract
Dendritic cell vaccines are a promising strategy for the treatment of cancer and infectious diseases but have met with mixed success. We report on a lentiviral vector-based dendritic cell vaccine strategy that generates a cluster of differentiation 8 (CD8) T cell response that is much stronger than that achieved by standard peptide-pulsing approaches. The strategy was tested in the mouse lymphocytic choriomeningitis virus (LCMV) model. Bone marrow-derived dendritic cells from SAMHD1 knockout mice were transduced with a lentiviral vector expressing the GP33 major-histocompatibility-complex (MHC)-class-I-restricted peptide epitope and CD40 ligand (CD40L) and injected into wild-type mice. The mice were highly protected against acute and chronic variant CL-13 LCMVs, resulting in a 100-fold greater decrease than that achieved with peptide epitope-pulsed dendritic cells. Inclusion of an MHC-class-II-restricted epitope in the lentiviral vector further increased the CD8 T cell response and resulted in antigen-specific CD8 T cells that exhibited a phenotype associated with functional cytotoxic T cells. The vaccination synergized with checkpoint blockade to reduce the viral load of mice chronically infected with CL-13 to an undetectable level. The strategy improves upon current dendritic cell vaccine strategies; is applicable to the treatment of disease, including AIDS and cancer; and supports the utility of Vpx-containing vectors.Entities:
Keywords: AIDS; CD8; LCMV; SAMHD1; Vpx; cancer; dendritic cell; lentiviral vector; vaccine
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Year: 2020 PMID: 32497512 PMCID: PMC7403335 DOI: 10.1016/j.ymthe.2020.05.018
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454