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