Oncogenic mutations in ras create HLA-A2.1 binding peptides but affect their extracellular antigen processing
Point mutations in oncogene products such as ras may create neoantigenic determinants recognizable by T lymphocytes as tumor antigens, that could be marshalled to eliminate a tumor by inducing specific cytotoxic T lymphocytes (CTL) with an appropriate vaccine. Peptide-pulsed dendritic cells are a pr...
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Veröffentlicht in: | International immunology 1997-08, Vol.9 (8), p.1085-1093 |
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