Expression of a natural tumor antigen by thymic epithelial cells impairs the tumor-protective CD4+ T-cell repertoire

R Bos, S Van Duikeren, T Van Hall, P Kaaijk, R Taubert… - Cancer research, 2005 - AACR
R Bos, S Van Duikeren, T Van Hall, P Kaaijk, R Taubert, B Kyewski, L Klein, CJM Melief
Cancer research, 2005AACR
A variety of antigens that display a highly tissue-specific expression pattern have recently
found to be also expressed in medullary thymic epithelial cells (mTEC). This unique feature
of mTEC plays an important role in preventing hazardous autoimmune responses through
thymic tolerization of T-cell subsets directed against autoantigens but could also limit the
possibility of exploiting tumor-associated antigens for immune-mediated targeting of
cancers. Our present study shows that expression of carcinoembryonic antigen (CEA) in …
Abstract
A variety of antigens that display a highly tissue-specific expression pattern have recently found to be also expressed in medullary thymic epithelial cells (mTEC). This unique feature of mTEC plays an important role in preventing hazardous autoimmune responses through thymic tolerization of T-cell subsets directed against autoantigens but could also limit the possibility of exploiting tumor-associated antigens for immune-mediated targeting of cancers. Our present study shows that expression of carcinoembryonic antigen (CEA) in thymic epithelial cells of CEA-transgenic mice results in tolerization of a major fraction of the CD4+ T-cell repertoire against this antigen, thereby markedly limiting the effect of CEA-specific immunization against CEA-overexpressing tumors. The expression of CEA in mTEC of CEA-transgenic mice is mirrored by its expression in human mTEC, arguing that promiscuous gene expression in these thymic stromal cells needs to be considered as a potential hurdle for immunotherapies of cancer that target tissue-specific autoantigens.
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