Peptide-pulsed MHC class II mutant dendritic cell vaccine has superior efficacy in a murine tumor model.
نویسندگان
چکیده
Abstract Autologous dendritic cell (DC) vaccines with tumor antigens have been used clinically limited therapeutic effects. Semi-allogeneic DC-based immunotherapy is still controversial, but it can be an alternative source and more attractive than autologous DC because the “off-the-shelf” DCs for multiple patients without lengthy individual manufacturing time may provide additional “allogeneic help”. This study aims to compare efficacy of syngeneic semi-allogeneic determine whether a vaccine efficacious in suppression. Female C57BL/6 mice were inoculated subcutaneously human papillomavirus E6 E7-expressing TC-1 cells. Syngeneic bone marrow cells (BMDCs) generated from BMDCs two mouse strains, B6.C-H2-K bm1/ByJ B6(C)-H2-Ab1 bm12/KhEgJ which had point mutations MHC class I H2-K ballele or H2-lA bMHC II allele, respectively. Each BMDC was pulsed H-2D b-restricted E7 43–77peptide matured before injection. The received 4 intradermal injections one E7-pulsed starting 8–9 days after implantation. Compared saline control, mutant similar suppressing growth. However, significantly superior that other vaccines. Thus, effective cancer vaccines, presumably alloantigens induce T help anti-tumor immunity.
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ژورنال
عنوان ژورنال: Journal of Immunology
سال: 2023
ISSN: ['1550-6606', '0022-1767']
DOI: https://doi.org/10.4049/jimmunol.210.supp.159.10