Publication | Open Access
Spontaneous human squamous cell carcinomas are killed by a human cytotoxic T lymphocyte clone recognizing a wild-type p53-derived peptide
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Citations
20
References
1996
Year
ImmunologyPathologyAntigen ProcessingImmunotherapeuticsImmunotherapyTumor BiologySynthetic ImmunologyWild-type P53-derived PeptideOncologyVitro PrimingP53 Protein-derived Self-epitopesRadiation OncologyCancer ResearchProtein-derived Wild-type PeptidesMalignant DiseaseCell BiologyTumor MicroenvironmentCancer ImmunosurveillanceHuman Cytotoxic TPeptide TherapeuticMedicine
A cytotoxic T lymphocyte (CTL) clone generated in vitro from the peripheral blood of a healthy HLA-A2-positive individual against a synthetic p53 protein-derived wild-type peptide (L9V) was shown to kill squamous carcinoma cell lines derived from two head and neck carcinomas, which expressed mutant p53 genes, in a L9V/HLA-A2 specific and restricted fashion. Thus, the normal tolerance against endogenously processed p53 protein-derived self-epitopes can be broken by peptide-specific in vitro priming. p53 protein-derived wild-type peptides might thus represent tumor associated target molecules for immunotherapeutical approaches.
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