Target intelligence / Profile preview

HLA class I histocompatibility antigen, A alpha chain (HLA-A*11:01) (HLA-A*11:01)

Target
HLA-A*11:01
Molecular classification
MHC Class I, Receptor, HLA-A*03 supertype
01

Overview

Human leukocyte antigen A*11:01 (HLA-A*11:01) is a highly prevalent MHC Class I allele, particularly within East Asian and Oceanian populations [1, 5, 12]. It encodes the alpha chain of the HLA-A*11:01 molecule, which forms a heterodimer with beta-2 microglobulin to present intracellularly derived peptides to CD8+ cytotoxic T cells [4, 20]. This allele is a significant therapeutic target in oncology, specifically for T-cell receptor (TCR) engineered T-cell therapies and cancer vaccines targeting "public" neoantigens such as KRAS G12V, PIK3CA H1047L, and mutated NPM1 [6, 9, 10, 11]. Beyond cancer, HLA-A*11:01 plays a vital role in the immune control of viral infections, including influenza A/B, HIV, and Epstein-Barr virus [1, 3, 8]. However, it is also clinically relevant in pharmacogenomics, as it is associated with an increased risk of severe drug-induced hypersensitivity reactions, such as Stevens-Johnson Syndrome, in response to medications like carbamazepine and isoniazid [2, 14]. Effective use of this target requires precise HLA typing and neoantigen screening to ensure therapeutic efficacy and minimize safety risks such as off-target toxicity or cytokine release syndrome [3, 16].

Other names
HLA-A11HLA-A*1101A11A*1101
02

Mechanism of action

Presentation of intracellularly derived peptides to CD8+ cytotoxic T cells for immune recognition and elimination of infected or malignant cells.

03

Biological functions

Antigen presentationImmune responseCD8+ T cell activation
04

Disease associations

CancerInfectionDrug hypersensitivity
05

Safety considerations

Off-target toxicityCytokine release syndrome (CRS)Drug-induced hypersensitivity (e.g., Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis)
06

Interacting drugs

AFNT-211

1 more in the full profile.

07

Biomarkers

HLA-A*11:01 genotypeKRAS G12V mutationPIK3CA H1047L mutationNPM1 mutation

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