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• W2045291287 startingPage "1658" @default.
• W2045291287 abstract "We have used bee venom phospholipase A 2 as a vector to load human dendritic cells ex vivo with a major histocompatibility complex (MHC) class I‐restricted epitope fused to its C‐terminus. The fusion protein bound to human monocyte‐derived dendritic cells and was internalized into early endosomes. In vitro immunization experiments showed that these dendritic cells were able to generate specific CD8 T cell lines against the epitope carried by the fusion protein. Cross‐presentation did not require proteasome, transporter associated with antigen processing, or endosome proteases, but required newly synthesized MHC molecules. Comparison of the antigen presentation pathway observed in this study to that followed by other toxins used as vectors is discussed." @default.
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• W2045291287 date "2005-02-19" @default.
• W2045291287 modified "2023-10-17" @default.
• W2045291287 title "Cross-presentation of a CMV pp65 epitope by human dendritic cells using bee venom PLA₂as a membrane-binding vector" @default.
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• W2045291287 doi "https://doi.org/10.1016/j.febslet.2005.02.019" @default.
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