Immunotherapy of cancer through targeting of the p53 tumor antigen

Arch Immunol Ther Exp (Warsz). 2002;50(5):297-305.

Abstract

The expression of the p53 tumor suppressor protein is frequently increased in a great variety of human cancers, making this antigen an attractive candidate for targeting therapeutic T cell immunity. However, potential complications as a result of immunological tolerance or autoimmune pathology must be taken into account when exploiting this ubiquitously expressed auto-antigen for the immunotherapy of cancer.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antigen Presentation
  • Antigens, Neoplasm / metabolism*
  • Autoimmunity
  • Colorectal Neoplasms / immunology
  • Colorectal Neoplasms / metabolism
  • Colorectal Neoplasms / therapy
  • Humans
  • Immune Tolerance
  • Immunotherapy / methods*
  • Neoplasms / immunology*
  • Neoplasms / metabolism
  • Neoplasms / therapy*
  • Nuclear Proteins*
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-mdm2
  • T-Lymphocytes, Helper-Inducer / immunology
  • Tumor Suppressor Protein p53 / immunology*

Substances

  • Antigens, Neoplasm
  • Nuclear Proteins
  • Proto-Oncogene Proteins
  • Tumor Suppressor Protein p53
  • MDM2 protein, human
  • Proto-Oncogene Proteins c-mdm2