# Targeting Telomerase in Cancer: Vaccine-Based Strategies, Clinical Evidence, and Synergy with Immunotherapy

**Authors:** Stella Baliou, Manolis N. Tzatzarakis, Andreas G. Tsantes, Elena Vakonaki, Petros Ioannou, Michalis Kyriakakis, Eleftheria Hatzidaki, Iordanis Pelagiadis, Eftichia Stiakaki, Aristides Tsatsakis

PMC · DOI: 10.3390/diseases14020080 · 2026-02-20

## TL;DR

This review explores how telomerase vaccines can target cancer cells and enhance immunotherapy by boosting T-cell responses.

## Contribution

The paper highlights the clinical potential of telomerase vaccines and their synergy with immunotherapy.

## Key findings

- Telomerase vaccines stimulate antigen-specific T-cell responses against cancer cells.
- Combining telomerase vaccines with immune checkpoint inhibitors improves therapeutic effectiveness.
- Clinical trials have tested various telomerase vaccine types, including DNA, mRNA, and cell-based vaccines.

## Abstract

With each replication cycle, telomeres shorten. Telomerase can slow or reverse the rate of telomere shortening. In the era of cancer immunotherapy, telomerase is a promising tumor-associated antigen due to its widespread and specific expression in cancer cells and its strong immunogenicity. Interestingly, telomerase-based vaccines eradicate telomerase-expressing cancer cells by increasing antigen-specific T-cell responses rather than by directly inhibiting telomerase enzymatic activity as telomerase inhibitors function. To support this, telomerase-based vaccines, including DNA, mRNA, peptide-, and cell-based vaccines, have been evaluated in clinical settings to elucidate their molecular mechanisms of action. The aim of this review is to present the clinical effectiveness of telomerase vaccines alone or in combination with immunotherapy. In particular, the therapeutic effectiveness of telomerase vaccines is influenced by the tumor microenvironment and can be substantially increased by combining them with immune checkpoint inhibitors. To further optimize telomerase-based vaccines, we discuss translational challenges and highlight the need for further optimization.

## Linked entities

- **Proteins:** tert.L (telomerase reverse transcriptase L homeolog)
- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Genes:** IDO1 (indoleamine 2,3-dioxygenase 1) [NCBI Gene 3620] {aka IDO, IDO-1, INDO}, TERF2IP (TERF2 interacting protein) [NCBI Gene 54386] {aka DRIP5, RAP1}, GAR1 (GAR1 ribonucleoprotein) [NCBI Gene 54433] {aka NOLA1}, TLR3 (toll like receptor 3) [NCBI Gene 7098] {aka CD283, IIAE2, IMD83}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, TINF2 (TERF1 interacting nuclear factor 2) [NCBI Gene 26277] {aka DKCA3, DKCA5, TIN2}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, BTK (Bruton tyrosine kinase) [NCBI Gene 695] {aka AGMX1, AT, ATK, BPK, IGHD3, IMD1}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, LAMP3 (lysosome associated membrane protein 3) [NCBI Gene 27074] {aka CD208, DC LAMP, DC-LAMP, DCLAMP, LAMP, LAMP-3}, MAGEA1 (MAGE family member A1) [NCBI Gene 4100] {aka CT1.1, MAGE1}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, FOXP3 (forkhead box P3) [NCBI Gene 50943] {aka AIID, DIETER, IPEX, JM2, PIDX, XPID}, CCL11 (C-C motif chemokine ligand 11) [NCBI Gene 6356] {aka SCYA11}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, POT1 (protection of telomeres 1) [NCBI Gene 25913] {aka CMM10, CRMCC3, GLM9, HPOT1, PFBMFT8, TPDS3}, TERF2 (telomeric repeat binding factor 2) [NCBI Gene 7014] {aka TRBF2, TRF2}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}, TLR7 (toll like receptor 7) [NCBI Gene 51284] {aka IMD74, SLEB17, TLR7-like}, TRBV20OR9-2 (T cell receptor beta variable 20/OR9-2 (non-functional)) [NCBI Gene 6962] {aka CDR3, TCRBV20S2, TCRBV2O, TCRBV2S2O}, LAMP1 (lysosome associated membrane protein 1) [NCBI Gene 3916] {aka CD107a, LAMPA, LGP120}, CD34 (CD34 molecule) [NCBI Gene 947], IFNA1 (interferon alpha 1) [NCBI Gene 3439] {aka IFL, IFN, IFN-ALPHA, IFN-alphaD, IFNA13, IFNA@}, CD1C (CD1c molecule) [NCBI Gene 911] {aka BDCA1, CD1, R7}, HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}, HSP90AA1 (heat shock protein 90 alpha family class A member 1) [NCBI Gene 3320] {aka EL52, HEL-S-65p, HSP86, HSP89A, HSP90A, HSP90N}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, IL2RA (interleukin 2 receptor subunit alpha) [NCBI Gene 3559] {aka CD25, IDDM10, IL2R, IMD41, TCGFR, p55}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, COX2 (cytochrome c oxidase subunit II) [NCBI Gene 808504], TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}, HSPA4 (heat shock protein family A (Hsp70) member 4) [NCBI Gene 3308] {aka APG-2, HEL-S-5a, HS24/P52, HSPH2, RY, hsp70}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, CTAG1A (cancer/testis antigen 1A) [NCBI Gene 246100] {aka CT6.1, ESO1, LAGE-2, LAGE2A, NY-ESO-1}, WT1 (WT1 transcription factor) [NCBI Gene 7490] {aka AWT1, GUD, NPHS4, WAGR, WIT-2, WT-1}, TPP1 (tripeptidyl peptidase 1) [NCBI Gene 1200] {aka CLN2, GIG1, LPIC, SCAR7, TPP-1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, ITGA5 (integrin subunit alpha 5) [NCBI Gene 3678] {aka CD49e, FNRA, VLA-5, VLA5A}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, MYC (MYC proto-oncogene, bHLH transcription factor) [NCBI Gene 4609] {aka MRTL, MYCC, bHLHe39, c-Myc}, KDR (kinase insert domain receptor) [NCBI Gene 3791] {aka CD309, FLK1, VEGFR, VEGFR2}, TERF1 (telomeric repeat binding factor 1) [NCBI Gene 7013] {aka PIN2, TRBF1, TRF, TRF1, hTRF1-AS, t-TRF1}, FASLG (Fas ligand) [NCBI Gene 356] {aka ALPS1B, APT1LG1, APTL, CD178, CD95-L, CD95L}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TERT (telomerase reverse transcriptase) [NCBI Gene 7015] {aka CMM9, DKCA2, DKCB4, EST2, PFBMFT1, TCS1}, CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}, CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, HAVCR2 (hepatitis A virus cellular receptor 2) [NCBI Gene 84868] {aka CD366, HAVcr-2, KIM-3, SPTCL, TIM3, TIMD-3}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, NOP10 (NOP10 ribonucleoprotein) [NCBI Gene 55505] {aka CHINE2, DKCB1, NOLA3, NOP10P, PFBMFT9}, PECAM1 (platelet and endothelial cell adhesion molecule 1) [NCBI Gene 5175] {aka CD31, CD31/EndoCAM, GPIIA', PECA1, PECAM-1, endoCAM}, CD28 (CD28 molecule) [NCBI Gene 940] {aka IMD123, Tp44}, VSIR (V-set immunoregulatory receptor) [NCBI Gene 64115] {aka B7-H5, B7H5, C10orf54, DD1alpha, Dies1, GI24}, CSF2 (colony stimulating factor 2) [NCBI Gene 1437] {aka CSF, GMCSF}, HLA-C (major histocompatibility complex, class I, C) [NCBI Gene 3107] {aka D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, TIGIT (T cell immunoreceptor with Ig and ITIM domains) [NCBI Gene 201633] {aka VSIG9, VSTM3, WUCAM}, FAS (Fas cell surface death receptor) [NCBI Gene 355] {aka ALPS1A, APO-1, APT1, CD95, FAS1, FASTM}
- **Diseases:** mesothelioma (MESH:D008654), Fatigue (MESH:D005221), T-cell leukemia (MESH:D015458), carcinogenesis (MESH:D063646), cutaneous melanoma (MESH:C562393), diarrhea (MESH:D003967), myalgia (MESH:D063806), rashes (MESH:D005076), hypoxic (MESH:D002534), breast adenocarcinoma (MESH:D001943), castration-resistant prostate cancer (MESH:D064129), autoimmune (MESH:D001327), nausea (MESH:D009325), NSCLC (MESH:D002289), pruritus (MESH:D011537), RCC (MESH:D002292), glioblastoma (MESH:D005909), hypoxia (MESH:D000860), prostate, pancreatic, and hematologic malignancies (MESH:D011472), malignant pleural mesothelioma (MESH:D000086002), solid (MESH:D018250), anaphylactic reaction (MESH:D000707), chronic (MESH:D002908), HCC (MESH:D006528), HPV-positive (MESH:D030361), AML (MESH:D015470), necrosis (MESH:D009336), pulmonary embolism (MESH:D011655), erythema (MESH:D004890), bone and soft-tissue sarcomas (MESH:D012509), myelodysplastic syndromes (MESH:D009190), fever (MESH:D005334), hematologic malignancies (MESH:D019337), neutropenia (MESH:D009503), cervical cancer (MESH:D002583), CTCL (MESH:D016410), III (MESH:C537189), flu (MESH:D007251), pain (MESH:D010146), autoimmune complications (MESH:D020274), hematologic toxicities (MESH:D006402), pancreatic and pulmonary cancers (MESH:D010190), urothelial carcinoma (MESH:D014523), CLL (MESH:D015451), CRC (MESH:D015179), headaches (MESH:D006261), inflammation (MESH:D007249), PDAC (MESH:D021441), anemia (MESH:D000740), injury to (MESH:D014947), metastases (MESH:D009362), PC (MESH:D011471), melanoma (MESH:D008545), fibrosis (MESH:D005355), gliomas (MESH:D005910), cytotoxic (MESH:D064420), Metastatic (MESH:D000092182), MSI (MESH:D053842), hyponatremia (MESH:D007010), hepatitis B (MESH:D006509)
- **Chemicals:** lipid (MESH:D008055), atezolizumab (MESH:C000594389), water (MESH:D014867), ibrutinib (MESH:C551803), 8-hydroxy-2-deoxyguanosine (MESH:D000080242), bevacizumab (MESH:D000068258), creatinine (MESH:D003404), docetaxel (MESH:D000077143), CTN (MESH:C403585), ROS (MESH:D017382), cyclophosphamide (MESH:D003520), CpG oligodeoxynucleotides (MESH:C408982), gemcitabine (MESH:D000093542), ipilimumab (MESH:D000074324), nivolumab (MESH:D000077594), imiquimod (MESH:D000077271), Montanide (MESH:C000712049), Montanide ISA-51 (MESH:C477385), DPX (MESH:C027512), GV001 (-), poly-IC:LC (MESH:C019531), imetelstat (MESH:C519562), 51-Chromium (MESH:C000615375), celecoxib (MESH:D000068579), oil (MESH:D009821), capecitabine (MESH:D000069287), lactate (MESH:D019344), cemiplimab (MESH:C000627974), temozolomide (MESH:D000077204), pembrolizumab (MESH:C582435)
- **Species:** Symbiodinium sp. Lp (species) [taxon 218554], Human papillomavirus (species) [taxon 10566], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** T572Y, 572Y, A-to-I, leucine (L) with tyrosine (Y), p988Y
- **Cell lines:** Vx-001 — Oryctolagus cuniculus (Rabbit), Rabbit neoplasm, Cancer cell line (CVCL_3864), GX301 — Homo sapiens (Human), Pituitary gland carcinoma, Cancer cell line (CVCL_ZV99)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12939409/full.md

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Source: https://tomesphere.com/paper/PMC12939409