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Telomerase reverse transcriptase (hTERT) is the catalytic subunit of the telomerase enzyme, which maintains telomere length and is essential for the unlimited proliferative capacity of cancer cells (Source: UniProt P09488). While hTERT is highly expressed in over 85% of all human cancers, its expression is negligible or absent in most normal adult somatic cells, making it a near-universal tumor-associated antigen (Source: PubMed PMID: 28633325). Peptide epitopes derived from hTERT are short amino acid sequences that can be presented by Major Histocompatibility Complex (MHC) molecules on the surface of tumor cells (Source: PubMed PMID: 11007150). These epitopes serve as targets for cancer immunotherapy, particularly in the development of therapeutic vaccines and adoptive T-cell therapies (Source: PubMed PMID: 31434351). By administering these peptides, the immune system is primed to generate hTERT-specific cytotoxic T lymphocytes (CTLs) and helper T cells that selectively target and destroy malignant cells (Source: PubMed PMID: 25103444). Clinical candidates like GV1001 and UV1 utilize these epitopes to treat various malignancies, including pancreatic, lung, and prostate cancers (Source: ClinicalTrials.gov).
Active immunotherapy through the presentation of hTERT-derived peptides by MHC molecules to T-cell receptors, stimulating the expansion of hTERT-specific cytotoxic and helper T cells to eliminate telomerase-positive tumor cells (Source: PubMed PMID: 20670951).
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