Tumor-specific shared antigenic peptides recognized by human T cells

Authors


Pierre van der Bruggen, Ludwig Institute for Cancer Research, 74 avenue Hippocrate UCL 74.59, B-1200 Brussels, Belgium
Tel: + 32 2764 74 31
Fax: + 32 2762 94 05
e-mail: pierre.vanderbruggen@bru.licr.org

Abstract

Summary: The first tumor-specific shared antigens and the cancer-germline genes that code for these antigens were identified with antitumor cytolytic T lymphocytes obtained from cancer patients. A few HLA class I-restricted antigenic peptides were identified by this ‘direct approach’. A large set of additional cancer-germline genes have now been identified by purely genetic approaches or by screening tumor cDNA expression libraries with the serum of cancer patients. As a result, a vast number of sequences are known that can code for tumor-specific shared antigens, but most of the encoded antigenic peptides have not yet been identified. We review here recent ‘reverse immunology’ approaches for the identification of new antigenic peptides. They are based on in vitro stimulation of naive T cells with dendritic cells that have either been loaded with a cancer-germline protein or that have been transduced with viruses carrying cancer-germline coding sequences. These approaches have led to the identification of many new antigenic peptides presented by class I or class II molecules. We also describe some aspects of the processing and presentation of these antigenic peptides.

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