Target intelligence / Profile preview

Major histocompatibility complex class I A*02 (HLA-A*02)

Target
HLA-A*02
Molecular classification
Receptor, Major histocompatibility complex class I molecule, Cell surface glycoprotein
01

Overview

Major histocompatibility complex class I A*02 (HLA-A*02) is a highly polymorphic cell surface glycoprotein belonging to the class I major histocompatibility complex family. It consists of a polymorphic heavy α chain and a non-polymorphic β2-microglobulin light chain, forming a platform for peptide binding. HLA-A*02 presents intracellularly derived peptides—most commonly from viruses or abnormal proteins—to cytotoxic CD8+ T lymphocytes, thereby enabling immune recognition and destruction of infected or malignant cells. This molecule is critical for adaptive immunity, transplantation compatibility, and serves as a common restriction element for T-cell therapeutic targeting, especially in cancer immunotherapy and vaccine development. In clinical therapeutics, its prevalence and peptide specificity make it a cornerstone in patient selection for T-cell receptor-directed therapies and peptide vaccines. Dysfunction or loss of HLA-A*02 expression can underlie immune evasion in tumors, while mismatch or inappropriate activation can present risks in autoimmunity and transplant rejection contexts.

Other names
HLA-A*02Human leukocyte antigen A*02HLA-A2 (historical/less precise)MHC class I A*02
02

Mechanism of action

Facilitation of cytotoxic T-cell recognition of presented peptides, leading to targeted cell death Presentation of intracellular (viral or tumor) peptides on the cell surface for immune detection Interactions with CD8 co-receptor to activate T-cell effector function

03

Biological functions

Antigen presentationImmune responseActivation of cytotoxic T lymphocytes (CD8+ T cells)Cell signaling in immune surveillanceInduction of apoptosis in infected or transformed cells
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Disease associations

Cancer (tumor antigen presentation)Infection (viral, intracellular pathogens)Autoimmune disease (peptide presentation can contribute)Transplantation (alloreactivity, graft rejection)
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Safety considerations

Off-target immune activation (autoimmunity)Graft-vs-host disease (transplant context)Limited population coverage (HLA-A*02 is not universal; population stratification required)Immune escape via loss/decreased expression on tumor cells
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Interacting drugs

4 more in the full profile.

07

Biomarkers

HLA typing in patient selection (especially for HLA-A*02–restricted immunotherapies)HLA-A*02 expression as a marker for eligibility for certain peptide vaccines and adoptive T-cell therapies

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