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Identification of a naturally processed T cell epitope derived from the glioma-associated protein SOX11.
Schmitz, Marc; Wehner, Rebekka; Stevanovic, Stefan; Kiessling, Andrea; Rieger, Michael A; Temme, Achim; Bachmann, Michael; Rieber, E Peter; Weigle, Bernd.
Afiliação
  • Schmitz M; Medical Faculty, Institute of Immunology, Technical University of Dresden, Fetscherstr. 74, 01307 Dresden, Germany. mschmitz@rcs.urz.tu-dresden.de
Cancer Lett ; 245(1-2): 331-6, 2007 Jan 08.
Article em En | MEDLINE | ID: mdl-16504379
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.
Assuntos
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Base de dados: MEDLINE Assunto principal: Proteínas de Grupo de Alta Mobilidade / Epitopos de Linfócito T / Glioma Idioma: En Ano de publicação: 2007 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Proteínas de Grupo de Alta Mobilidade / Epitopos de Linfócito T / Glioma Idioma: En Ano de publicação: 2007 Tipo de documento: Article