Human p53(264-272) HLA-A2 binding peptide is an immunodominant epitope in DNA-immunized HLA-A2 transgenic mice.

Abstract:

:C57BL/10 mice transgenic for HLA-A2 were immunized with either a full-length DNA-construct of the tumor suppressor p53 or with a minigene encoding the p53-derived immunodominant peptide p53(264)LLGRNSFEV272 (L9V). Vaccination with the full-length p53 construct induced potent cytotoxic activity of splenocytes against L9V-pulsed target cells after in vivo re-stimulation. Vaccination with the L9V-encoding minigene likewise induced specific anti-L9V cytotoxicity in vitro. Subsequent experiments revealed that peptide-pulsed dendritic cells were the most efficient cell types for in vitro re-stimulation. In concordance with this, immunization with L9V-pulsed dendritic cells also induced a potent and specific anti-L9V cytotoxic response in vitro. These data show that HLA-A2/peptide-specific cytotoxic immunity can be generated in vivo against the same immunodominant epitope by immunizing either with full-length DNA or with a DNA minigene encoding the immunodominant peptide epitope.

journal_name

Cancer Lett

journal_title

Cancer letters

authors

Petersen TR,Bregenholta S,Pedersen LO,Nissen MH,Claesson MH

doi

10.1016/s0304-3835(98)00353-x

keywords:

subject

Has Abstract

pub_date

1999-04-01 00:00:00

pages

183-91

issue

2

eissn

0304-3835

issn

1872-7980

pii

S0304-3835(98)00353-X

journal_volume

137

pub_type

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