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• W2024146645 abstract "Dendritic cells (DC) are the most potent antigen presenting cells whose ability to interact with T cells, B cells and NK cells has led to their extensive use in vaccine design. Here, we designed a DC-based HIV-1 vaccine using an attenuated rabies virus vector expressing HIV-1 Gag (RIDC-Gag). To test this, BALB/c mice were immunized with RIDC-Gag, and the primary, secondary as well as humoral immune responses were monitored. Our results indicate that RIDC-Gag stimulated HIV-1 Gag-specific immune responses in mice. When challenged with vaccinia virus (VV) expressing HIV-1 Gag, they elicited a potent Gag-specific recall response characterized by CD8+ T cells expressing multiple cytokines that were capable of specifically lysing Gag-pulsed target cells. Moreover, RIDC-Gag also enhanced CD8+ T cell responses via a homologous prime-boost regimen. These results show that a DC-based vaccine using live RV is immunogenic and a potential candidate for a therapeutic HIV-1 vaccine." @default.
• W2024146645 created "2016-06-24" @default.
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• W2024146645 date "2010-12-01" @default.
• W2024146645 modified "2023-09-26" @default.
• W2024146645 title "Dendritic cells infected by recombinant rabies virus vaccine vector expressing HIV-1 Gag are immunogenic even in the presence of vector-specific immunity" @default.
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• W2024146645 doi "https://doi.org/10.1016/j.vaccine.2010.08.042" @default.
• W2024146645 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2997164" @default.
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