Target intelligence / Profile preview

Human leukocyte antigen class I histocompatibility antigen, A-24 alpha chain (HLA-A24)

Target
HLA-A24
Molecular classification
Major histocompatibility complex (MHC) class I molecule, Receptor, Cell-surface antigen-presenting molecule
01

Overview

HLA-A24 is a member of the human leukocyte antigen (HLA) class I family, encoded by the HLA-A*24 allele group. It is a highly polymorphic membrane glycoprotein composed of an α chain (encoded by the HLA-A gene) associated non-covalently with β2-microglobulin. HLA-A24’s primary function is to present endogenous peptide fragments (from proteins within the cytoplasm, such as viral or tumor antigens) to CD8+ cytotoxic T lymphocytes, initiating immune responses against infected or malignant cells. Its distribution varies widely among human populations and it plays a crucial role in immune surveillance, organ transplantation compatibility, and the pathogenesis of various autoimmune diseases and and cancers. Due to its immunological specificity, HLA-A24 is a key stratification and selection marker in immunotherapies, particularly peptide-based cancer vaccines and T cell therapies.

Other names
HLA-A*24HLA A24A24Human leukocyte antigen A24HLA class I histocompatibility antigen A-24
02

Mechanism of action

For peptide vaccines and immunotherapies: HLA-A24 displays synthetic or tumor-derived peptides to activate or expand cytotoxic T lymphocytes specific for cancer cells or infected cells. Cellular therapies: HLA-A24-restriction is critical for the selection of TCR-engineered T cells and adoptive therapy candidates.

03

Biological functions

Antigen presentation: Presents intracellular peptide antigens (typically 8–10 amino acids) to cytotoxic T lymphocytes (CD8+ T cells)Immune response regulation: Activates CD8+ T cells, enabling immune recognition and elimination of virus-infected or malignant cellsSelf-vs-nonself discrimination: Permits immune tolerance of self-proteins, primarily through thymic selection
04

Disease associations

Cancer: HLA-A24-presented tumor antigens can be immunotherapy targetsInfection: HLA-A24 presents viral peptides (e.g., from Epstein-Barr virus, HIV, and others)Autoimmune diseases: Associated with increased risk for Type 1 Diabetes, Systemic Lupus Erythematosus, myasthenia gravis, and Buerger's diseaseOther: Transplant immunology (organ donor compatibility and graft-versus-host disease), population genetics/anthropology
05

Safety considerations

Autoimmunity: Some HLA-A24 alleles are associated with increased risk of autoimmune diseaseAlloimmunization in transplantation: Mismatched HLA can provoke graft rejection or graft-versus-host diseaseVaccine specificity/limited applicability: HLA-restricted vaccines are relevant only for individuals expressing the respective allele, limiting broad utility
06

Interacting drugs

No direct-acting small molecule drugs; however, HLA-A24-specific epitopes guide the design of cancer vaccines, peptide immunotherapies, and T-cell therapies

1 more in the full profile.

07

Biomarkers

HLA-A24 expression: Used to select patients likely to benefit from HLA-A24-restricted immunotherapies, peptide vaccines, or cytotoxic T-cell monitoring in cancer and infectious diseasesHLA typing: A clinical biomarker for disease susceptibility, prognosis, and adverse drug reaction risk

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