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Tumor cells expressing the L523S mutation represent a specific target for cytotoxic T lymphocytes (CTLs). The L523S mutation results in the presentation of a novel peptide antigen by MHC-I molecules on the tumor cell surface, which can be recognized by CTLs. This interaction triggers CTL activation and subsequent killing of the tumor cell through mechanisms such as perforin/granzyme release and Fas/FasL interaction. The effectiveness of this response is modulated by factors such as the density of antigen-specific CTLs, the expression level of L523S, and the presence of immunosuppressive factors within the tumor microenvironment.
Targeted for lysis by cytotoxic T lymphocytes (CTLs) through recognition of L523S-derived peptides presented on MHC-I.
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