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KRAS G13D mutant neoantigens are tumor-specific peptides derived from the KRAS protein with a glycine-to-aspartic acid substitution at position 13. These peptides are processed and presented on the surface of cancer cells by Human Leukocyte Antigen (HLA) molecules, making them targets for the adaptive immune system. Unlike wild-type KRAS, these neoantigens are not expressed in normal tissues, providing a high degree of tumor specificity for immunotherapies. Therapeutic strategies include cancer vaccines (mRNA or peptide-based) and adoptive T-cell therapies (TCR-T) designed to recognize the specific peptide-HLA complex. The G13D mutation is particularly prevalent in colorectal cancer and is associated with distinct signaling properties compared to G12 mutations.
Induction of a T-cell mediated immune response specifically against cancer cells presenting the KRAS G13D mutant peptide on HLA molecules, leading to targeted tumor cell lysis.
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