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Vaccination with cytotoxic T lymphocyte epitope‐containing peptide protects against a tumor induced by human papillomavirus type 16‐transformed cells

European Journal of Immunology · 1993 · Vol. 23(9) · pp. 2242–2249
Mariet C.W. FeltkampHenk L. SmitsMichel VierboomRené MinnaarB. M. de JonghJan W. DrijfhoutJan ter ScheggetCornelis J.M. MeliefW. Martin Kast

Abstract

Cytotoxic T lymphocyte (CTL) peptide epitopes can be used for immunization of mice against lethal virus infection. To study whether this approach can be successful against virus-induced tumors we generated a B6 (H-2b) tumorigenic cell line transformed by human papillomavirus (HPV). This virus is detected in over 90% of all human cervical cancers. To identify vaccine candidates, we generated a set of 240 overlapping peptides derived from the HPV type 16 (HPV16) oncogenes E6 and E7. These peptides were tested for their ability to bind H-2Kb and H-2Db MHC class I molecules. Binding peptides were compared with the presently known peptide-binding motifs for H-2Kb and H-2Db and the predictive value of these motifs is shortly discussed. The high-affinity H-2Db-binding peptide and putative CTL epitope E7 49-57 (RAHYNIVTF) was used in vaccination studies against HPV 16-transformed tumor cells. Immunization with peptide E7 49-57 rendered mice insensitive to a subsequent challenge with HPV 16-transformed tumor cells in vivo, and induced a CTL response which lysed the tumor cells in vitro.

Immunotherapy and Immune Responsesvaccines and immunoinformatics approachesVirus-based gene therapy researchEpitopeCTL*Cytotoxic T cellBiologyVirologyPeptideMHC class IAntigenImmunizationIn vitro

MeSH terms

Amino Acid SequenceAnimalsEpitopesCell LineCell Line, TransformedMice, Inbred BALB CMolecular Sequence DataOncogene Proteins, ViralPeptide FragmentsRepressor ProteinsT-Lymphocytes, CytotoxicTumor Virus InfectionsVaccinationViral VaccinesHistocompatibility Antigens Class I
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