Target intelligence / Profile preview

Human telomerase reverse transcriptase-derived peptide–Human leukocyte antigen-A*02:01 complex (hTERT-peptide–HLA-A*02:01)

Target
hTERT-peptide–HLA-A*02:01
Molecular classification
Antigen, Peptide-MHC complex, MHC Class I complex
01

Overview

The hTERT-derived peptide–HLA-A*02:01 complex is a tumor-associated antigen (TAA) consisting of a short peptide fragment from the human telomerase reverse transcriptase (hTERT) protein bound to the Human Leukocyte Antigen (HLA) allele A*02:01 [NIH, 2004]. hTERT is the catalytic subunit of telomerase, an enzyme responsible for maintaining telomere length, which is upregulated in over 85% of human cancers to enable replicative immortality [NIH, 2012; BMJ, 2022]. Because hTERT expression is minimal in most healthy adult tissues, this complex serves as a selective target for cancer immunotherapy [NIH, 2008]. Therapeutic strategies targeting this complex include peptide-based vaccines such as Vx-001 and UV1, which aim to elicit a specific cytotoxic T cell (CTL) response against hTERT-expressing tumor cells [NCI, 2023; BMJ, 2022]. Additionally, adoptive T-cell therapies using engineered T-cell receptors (TCRs) are being developed to recognize and lyse cells presenting these specific epitopes [NIH, 2012]. However, the clinical utility of certain epitopes, such as hTERT(540-548), is a subject of ongoing research due to evidence suggesting they may not be efficiently processed or naturally presented on the surface of all tumor types [NIH, 2004; NIH, 2005].

Other names
hTERT/HLA-A2 complexhTERT-derived peptide–HLA-A2 complexTERT-peptide–HLA-A*02:01hTERT(540-548)/HLA-A*02:01hTERT(572-580)/HLA-A*02:01hTERT(865-873)/HLA-A*02:01hTERT(540-548) peptide–HLA-A*02:01 complex
02

Mechanism of action

Induction of peptide-specific CD8+ cytotoxic T lymphocytes (CTLs) that recognize the hTERT-peptide–HLA-A*02:01 complex on the surface of tumor cells, leading to targeted cell lysis and antitumor immune responses.

03

Biological functions

Antigen presentationT cell activationImmune recognition
04

Disease associations

Cancer
05

Safety considerations

Potential off-target toxicity to hTERT-expressing normal cells (e.g., hematopoietic stem cells)Inefficient natural processing and presentation of certain epitopesImmune exhaustion of induced T cells
06

Interacting drugs

Vx-001

3 more in the full profile.

07

Biomarkers

HLA-A*02:01 genotypehTERT mRNA expressionTelomerase activityhTERT-specific T cell frequency

Beyond the preview

Go deeper on Human telomerase reverse transcriptase-derived peptide–Human leukocyte antigen-A*02:01 complex (hTERT-peptide–HLA-A*02:01).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Human telomerase reverse transcriptase-derived peptide–Human leukocyte antigen-A*02:01 complex (hTERT-peptide–HLA-A*02:01).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call