Author/Authors :
Schmitz، نويسنده , , Marc and Wehner، نويسنده , , Rebekka and Stevanovic، نويسنده , , Stefan and Kiessling، نويسنده , , Andrea and Rieger، نويسنده , , Michael A. and Temme، نويسنده , , Achim and Bachmann، نويسنده , , Michael and Rieber، نويسنده , , E. Peter and Weigle، نويسنده , , Bernd، نويسنده ,
Abstract :
The development of T cell-based immunotherapies of cancer depends on the identification of tumor-associated antigens capable of eliciting tumor-directed cytotoxic T cell responses. In malignant glioma the number of well-defined target antigens for cytotoxic T lymphocytes (CTLs) is still very limited. Recently, we demonstrated the abundant and specific overexpression of the transcription factor SOX11 in malignant glioma. Here, we describe the SOX11-derived peptide LLRRYNVAKV which is capable of inducing human leukocyte antigen-A*0201-restricted and tumor-reactive CTLs. This novel CTL epitope may serve as an attractive candidate for a T cell-based immunotherapy of glioma.
Keywords :
Tumor Antigen , immunotherapy , dendritic cells , Glioma , T cells