Target intelligence / Profile preview

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

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

Overview

Major histocompatibility complex class I A*02 molecule (HLA-A*02) is a highly polymorphic cell surface glycoprotein encoded by the HLA-A gene, found on all nucleated human cells. It is a member of the major histocompatibility complex class I family, consisting of a polymorphic α chain (with α1, α2, and α3 domains) non-covalently associated with β2-microglobulin. HLA-A*02 binds peptide fragments (8–10 amino acids, derived from intracellular proteins) in its α1/α2 domain groove and presents them at the cell surface. The presented peptide-HLA complex is recognized by the T cell receptor of cytotoxic CD8+ T lymphocytes, enabling immune surveillance against infected or transformed (e.g., cancerous) cells. HLA-A*02 and other class I molecules are essential for immune system discrimination of self versus non-self, play key roles in the outcome of viral infections, autoimmunity, immunotherapy, and determine compatibility in organ transplantation. Its high allelic diversity (notably A*02:01, A*02:06, etc.) contributes to individual variability in immune responses and influences susceptibility and resistance to various diseases

Other names
HLA-A*02HLA-A2HLA class I A*02HLA-A*02:01 (most common allele)MHC class I A2
02

Mechanism of action

Peptide/hapten presentation to CD8+ T cells, triggering cytotoxic immune responses Targeted killing of cells displaying abnormal/self/non-self peptides presented on HLA-A*02 by engineered T cells, bispecific antibodies, or vaccines

03

Biological functions

Antigen presentation to cytotoxic T cellsImmune surveillanceInduction of programmed cell death (apoptosis) in infected or abnormal cellsInitiation of adaptive immune response
04

Disease associations

Cancer (immune evasion, immunotherapy target)Infection (viral, bacterial, and some parasitic diseases)Transplant rejectionAutoimmunity
05

Safety considerations

Potential for autoimmune cytotoxicity if normal cells express immunogenic peptidesRisk of graft-versus-host disease or organ rejection during transplantationTumor immune escape by downregulation or loss of HLA-A*02 expression
06

Interacting drugs

Talimogene laherparepvec (induces immunogenic cell death, modulates antigen presentation)

3 more in the full profile.

07

Biomarkers

HLA-A*02 genotype (patient selection for peptide-directed therapies or T cell therapies)Expression level on tumors (predictive for immunotherapy response)Loss of HLA class I as a resistance biomarker for immune therapies

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