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Human leukocyte antigen A2-restricted tumor neoantigen (HLA-A2-restricted tumor neoantigen) (HLA-A2 neoantigen)

Target
HLA-A2 neoantigen
Molecular classification
Antigen, Other (Peptide-MHC complex)
01

Overview

Human leukocyte antigen A2-restricted tumor neoantigens are a class of highly specific cancer antigens formed by somatic mutations in the tumor genome and presented on the cell surface by the HLA-A*02:01 molecule [Schumacher & Schreiber, Science, 2015]. Because these antigens arise from mutations unique to the tumor, they are not expressed in healthy tissues, making them ideal targets for precision immunotherapy with minimal off-target effects [Blass & Ott, Nat Rev Clin Oncol, 2021]. These neoantigens are recognized by the T-cell receptor (TCR) of CD8+ cytotoxic T cells, triggering a targeted immune response against the malignant cells [Yadav et al., Nature, 2014]. Therapeutic strategies leveraging these targets include personalized mRNA vaccines, TCR-engineered T-cell (TCR-T) therapies, and neoantigen-specific monoclonal antibodies or bispecifics [Rojas et al., Nature, 2023]. The effectiveness of these therapies often depends on the patient's HLA-A2 status and the presence of high-quality, immunogenic mutations within the tumor [Ott et al., Nature, 2017]. However, challenges such as tumor heterogeneity and the loss of HLA expression can lead to immune escape and treatment resistance [McGranahan et al., Science, 2017].

Other names
HLA-A*02:01 restricted neoantigenMHC class I-restricted tumor-specific antigenTumor-specific neoepitopeTSANeoantigen-HLA-A2 complex
02

Mechanism of action

Therapeutic agents target these neoantigens by either delivering the mutated peptide sequences (vaccines) or engineering T cells to express receptors (TCR-T) that specifically recognize the peptide-HLA-A2 complex, thereby inducing a cytotoxic immune response against tumor cells [Blass & Ott, Nat Rev Clin Oncol, 2021].

03

Biological functions

Immune responseOther (Antigen presentation)Other (T-cell activation)
04

Disease associations

Cancer
05

Safety considerations

Off-target toxicity (cross-reactivity with self-peptides) [Linette et al., Blood, 2013]Cytokine release syndrome (CRS) [Norelli et al., Nat Med, 2018]HLA downregulation or loss [McGranahan et al., Science, 2017]Antigenic drift and immune escape [Sade-Feldman et al., Nat Commun, 2017]
06

Interacting drugs

mRNA-4157 (V940) [Weber et al., Lancet, 2024]

4 more in the full profile.

07

Biomarkers

HLA-A*02:01 genotype [Gonzalez-Galarza et al., Nucleic Acids Res, 2020]Tumor Mutational Burden (TMB) [Chalmers et al., Genome Med, 2017]Neoantigen load [Hellmann et al., N Engl J Med, 2018]CD8+ T-cell infiltration [Tumeh et al., Nature, 2014]

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