Target intelligence / Profile preview

Personalized cancer neoantigen (Neoantigen)

Target
Neoantigen
Molecular classification
Antigen, Peptide, MHC-restricted ligand
01

Overview

Personalized cancer neoantigens are unique proteins derived from non-synonymous somatic mutations, such as single nucleotide variants or frameshifts, that occur exclusively within a patient's tumor cells (Nature, 2017, 547:222-226). Because these antigens are not expressed in healthy tissues, they are not subject to central immune tolerance, making them highly potent targets for immunotherapy with a low risk of autoimmune toxicity (NCI, 2023). These neoepitopes are processed and presented on the cell surface by Major Histocompatibility Complex (MHC) molecules, where they can be recognized by CD8+ and CD4+ T cells (Science, 2015, 348:1245-1249). Therapeutic strategies targeting these antigens include personalized mRNA, DNA, or peptide vaccines, as well as adoptive T-cell therapies using TCR-engineered cells (Frontiers in Immunology, 2020, 11:568005). By identifying these mutations through genomic sequencing and bioinformatics, clinicians can develop custom treatments that stimulate a robust, tumor-specific immune response. This approach is particularly effective in tumors with high mutational burdens, though it faces challenges regarding manufacturing speed and tumor heterogeneity (Journal of Hematology & Oncology, 2019, 12:93).

Other names
Tumor-specific antigen (TSA)NeoepitopeSomatic mutation-derived antigenPatient-specific neoantigen
02

Mechanism of action

Induction of tumor-specific T-cell responses through the presentation of patient-specific mutated peptides on MHC molecules, leading to targeted destruction of malignant cells (Nature Reviews Cancer, 2021, 21:283-300).

03

Biological functions

Immune responseAntigen presentationT-cell activationAdaptive immunity
04

Disease associations

CancerMelanomaNon-small cell lung cancerPancreatic cancerColorectal cancer
05

Safety considerations

Immune-related adverse events (irAEs)Injection site reactionsManufacturing delays (vein-to-vein time)Tumor antigen loss (immune escape)Cytokine release syndrome (CRS)
06

Interacting drugs

mRNA-4157 (V940)

6 more in the full profile.

07

Biomarkers

Tumor Mutational Burden (TMB)HLA typingMicrosatellite Instability (MSI) statusNeoantigen loadCD8+ T-cell infiltration density

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