Target intelligence / Profile preview

Hepatitis C virus nonstructural protein 3 epitope 1406–1415 (HCV NS3 1406 epitope)

Target
HCV NS3 1406 epitope
Molecular classification
Epitope, Viral antigen, Peptide antigen
01

Overview

The Hepatitis C virus nonstructural protein 3 epitope 1406–1415 (commonly known as the HCV NS3 1406 epitope) is an immunodominant, HLA-A*02-restricted peptide within the NS3 protein of HCV. Its most recognized prototype sequence is KLSGLGLNAV, although multiple naturally occurring variants (e.g., KLSSLGLNAV, KLSGLGINAV, KLSALGLNAV) exist due to the high mutation rate of HCV[1][2][7]. This epitope is a principal target for CD8+ cytotoxic T lymphocytes, contributing to viral clearance during acute infection and associated with immune exhaustion in chronic infection. Sequence variability in this epitope facilitates viral immune escape, influencing disease persistence and presenting a significant barrier to effective T cell-based vaccines[1][2][7]. Chronic HCV infection is characterized by increased PD-1/Tim-3 expression on CD8+ T cells responding to this epitope, indicative of T cell exhaustion[1]. This region is a focus of immunotherapeutic and vaccine research, although no approved drugs currently target it directly[1][2][3][7].

Other names
NS3 1406HCV NS3 1406–1415 epitopeHCV 1406 epitopeNS3 1406–1415HCV NS3 KLSGLGLNAV (prototype sequence)HLA-A*02-restricted NS3 1406 epitope
02

Mechanism of action

Target of vaccine candidate CD8+ T cell responses (experimental: T cell-based immunotherapy and vaccine research); Site of immune escape via viral mutation; Elicits HLA-A*02:01-restricted cytotoxic T lymphocyte (CTL) responses

03

Biological functions

Immune recognition by CD8+ T cellsInduction of cytotoxic T cell responseImmune escape (via sequence variation)Adaptive immune response modulation
04

Disease associations

Infection (Hepatitis C virus infection)Immune escape/contributor to chronic infection
05

Safety considerations

High sequence variability leading to immune escape and vaccine challengeEpitope loss, immune evasion, and variable immunogenicity after mutation
06

Biomarkers

CD8+ T cell responses specific for NS3 1406 (immune monitoring during infection or after vaccination)PD-1/Tim-3 co-expression on HCV-specific CD8+ T cells (T cell exhaustion marker)

Beyond the preview

Go deeper on Hepatitis C virus nonstructural protein 3 epitope 1406–1415 (HCV NS3 1406 epitope).

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 Hepatitis C virus nonstructural protein 3 epitope 1406–1415 (HCV NS3 1406 epitope).

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