| Literature DB >> 30704821 |
Alfredo Amador-Molina1, Cesar Trejo-Moreno1, Damaris Romero-Rodríguez2, Isabel Sada-Ovalle2, Enrique Pérez-Cárdenas1, Edmundo Lamoyi3, José Moreno4, Marcela Lizano5.
Abstract
CD8+ T cell-mediated immune response plays a major role in the clearance of virus-infected cells, including human papillomavirus (HPV). The effective treatment of women with normal cytology but persistent high risk-HPV infection or with low-grade intraepithelial lesions could take advantage of novel strategies based on vaccination with viral immunological targets with a wide spectrum of cross-protection. The helicase E1, expressed early during viral replication in HPV infection, is among the most conserved papillomavirus proteins, which makes it a good vaccine candidate. In the present study, we examined E1-specific CD8+ T cell and NK immune responses in a mouse model with α-galactosylceramide (α-GalCer) as an adjuvant. We found that mice immunized with E1 combined with α-GalCer elicited an E1-specific CD8+ T and NK cell cytotoxic responses, which correlated with growth inhibition of grafted melanoma B16-F0 cells expressing E1, both in prophylactic and therapeutic protocols.Entities:
Keywords: Cytotoxic CD8+ T cells; E1 protein; Human papillomavirus; NK cells; α-galactosylceramide
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Year: 2019 PMID: 30704821 DOI: 10.1016/j.vaccine.2018.12.036
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641