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Neoantigen-Human Leukocyte Antigen complex (NeoAg-HLA) (NeoAg-HLA)

Target
NeoAg-HLA
Molecular classification
Major Histocompatibility Complex, Antigen-presenting complex
01

Overview

Neoantigen-Human Leukocyte Antigen (HLA) complexes are molecular structures on the surface of tumor cells consisting of a mutated peptide (neoantigen) bound to an HLA molecule. These complexes arise from somatic mutations—such as non-synonymous single nucleotide variants (SNVs), insertions/deletions (indels), or frameshifts—that are unique to the cancer genome and absent in healthy tissue (Nature Reviews Cancer, 2021). Because they are not subject to central thymic tolerance, neoantigen-HLA complexes are highly immunogenic and serve as ideal targets for precision immunotherapy (Science, 2017). Therapeutic approaches targeting these complexes include personalized neoantigen vaccines, which prime the patient's immune system to recognize these specific markers, and adoptive cell therapies like TCR-engineered T cells (TCR-T) that are programmed to bind the complex with high affinity (Journal of Hematology & Oncology, 2024). Despite their potential, the effectiveness of targeting these complexes can be hindered by tumor heterogeneity and the loss of HLA expression, which allows cancer cells to evade immune detection (Cell, 2019).

Other names
Neoepitope-HLA complexTumor-specific antigen-MHC complexMutant peptide-HLA complexpHLANeoantigen-MHC complex
02

Mechanism of action

Induction of a targeted T-cell response through the recognition of tumor-specific mutant peptides presented by HLA molecules, leading to selective destruction of malignant cells.

03

Biological functions

Antigen presentationImmune responseT-cell activationImmune surveillance
04

Disease associations

Cancer
05

Safety considerations

Off-target cross-reactivity with wild-type peptidesHLA downregulation or loss of heterozygosityCytokine release syndromeTumor antigen escape
06

Interacting drugs

mRNA-4157 (V940)

4 more in the full profile.

07

Biomarkers

Tumor Mutational Burden (TMB)HLA-A/B/C genotypeNeoantigen loadMicrosatellite instability (MSI)T-cell receptor (TCR) repertoire

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