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Tumor-associated antigen peptides are short peptides derived from self proteins that are overexpressed, differentiation-restricted, or cancer–testis restricted in tumors and presented on HLA class I molecules on cancer cells and extracellular vesicles; they can elicit CD8+ T-cell responses and are used as targets for cancer immunotherapies, but because many TAAs are also expressed at lower levels in some normal tissues, targeting them carries risks of on-target/off-tumor toxicity and variable immunogenicity.[6][3][2]
Vaccine-induced T-cell activation against TAA-derived peptides; CAR-T or TCR-T cell recognition of peptide–HLA complexes; Immune checkpoint blockade that augments T-cell responses to TAA peptides
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