Target intelligence / Profile preview

HPV16 E7 peptide–HLA-A*02:01 complex (null)

Target
null
Molecular classification
Peptide–MHC class I ligand complex, Antigenic epitope, Immune receptor ligand
01

Overview

The **HPV16 E7 peptide–HLA-A*02:01 complex** consists of a short (typically 8–11 amino acids; sometimes longer) peptide derived from the E7 oncoprotein of Human papillomavirus 16, presented by the major histocompatibility complex class I molecule HLA-A*02:01 on the surface of human cells[5][8]. This complex serves as a crucial antigen for cytotoxic T lymphocytes, allowing the immune system to recognize and destroy HPV-infected or transformed cells. It is a prominent target in immunotherapy research, most notably in cancer vaccine and adoptive cell transfer approaches for HPV16-driven cancers. Recent studies have verified both the stability of the complex and its immunogenicity, and therapeutic constructs (antibodies, T-cell receptors) have been engineered to specifically target the complex for directed immune attack[3][5]. The clinical utility and safety depend strongly on patient HLA subtype and tumor antigen expression.

Other names
HPV16 E7/HLA-A*02:01 complexHPV16 E7 peptide–MHC class I complex (where MHC class I is HLA-A*02:01)HPV type 16 E7 peptide–HLA-A*02:01HPV16 E7–HLA-A2 complex (less precise, but commonly seen)
02

Mechanism of action

Immune cell-based recognition: cytotoxic T lymphocytes bind to the peptide–HLA complex via their T-cell receptor, leading to targeted killing of infected/malignant cells[5][3] Antibody-mediated blockade or recruitment (by engineered antibodies that mimic T-cell receptor binding of the complex)[3]

03

Biological functions

Antigen presentationImmune response activation (primarily cytotoxic T lymphocyte recognition)Tumor immune surveillance
04

Disease associations

Cancer (especially cervical and other HPV16-associated cancers, e.g., head and neck)Infection (HPV16 infection, viral immune evasion mechanisms)
05

Safety considerations

Off-target toxicity (potential for autoimmunity if similar peptide–MHC complexes are present in healthy tissues)HLA-restriction (therapy effective only in HLA-A*02:01-positive patients)Immune evasion (tumor downregulation of HLA-A*02:01 or loss of antigenicity causing reduced efficacy)
06

Interacting drugs

Experimental T-cell receptor mimic antibodies (e.g., anti-E7MC constructs targeting this complex)

2 more in the full profile.

07

Biomarkers

HLA-A*02:01 positivity (for patient selection in immunotherapies)HPV16 E7 epitope-specific T-cell responses (monitoring efficacy of immunotherapies)

Beyond the preview

Go deeper on HPV16 E7 peptide–HLA-A*02:01 complex (null).

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 HPV16 E7 peptide–HLA-A*02:01 complex (null).

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