Target intelligence / Profile preview

PRAME peptide-HLA-A*24:02 complex

Molecular classification
Other (peptide-MHC complex), Immune complex, Antigen presentation complex
01

Overview

The **PRAME peptide-HLA-A*24:02 complex** is a molecular complex consisting of a peptide derived from the cancer-testis antigen PRAME (Preferentially Expressed Antigen in Melanoma), bound in the groove of the major histocompatibility complex class I molecule HLA-A*24:02. PRAME is expressed at high levels in multiple malignancies (including leukemias and solid tumors), but is typically absent from most normal adult tissues except testes[4][5][6]. The PRAME peptide is processed intracellularly and presented on the surface of tumor cells by HLA-A*24:02, where it can be specifically recognized by T cell receptors or engineered antibodies. This complex serves as a therapeutic target in cancer immunotherapy, enabling the development of TCR-engineered T cells, TCR-mimic antibodies, and other modalities aimed at harnessing the immune system to eliminate PRAME-expressing tumor cells with specificity dictated both by tumor antigen expression and by HLA type[2][4][6].

Other names
PRAME/HLA-A*24:02 complexPRAME peptide-MHC class I complexPRAME-A24 complex
02

Mechanism of action

TCR or antibody binding to the PRAME-HLA-A*24:02 complex leads to T cell activation and lysis of PRAME-expressing tumor cells[2][6]. Engineered T cells (e.g., TCR-T) or TCR-mimic antibodies recognize PRAME peptide presented by HLA-A*24:02 on tumor cells, leading to immune-mediated tumor killing[2][6].

03

Biological functions

Immune responseAntigen presentationTumor-specific immune recognition
04

Disease associations

Cancer (including leukemia, solid tumors)Other (tumor immunity)
05

Safety considerations

Potential for off-target effects if the targeted PRAME peptide-HLA complex is expressed on normal tissues, though PRAME is generally low or absent in healthy adult tissues[2][3][4][6].Immune-related adverse effects due to on-target, off-tumor toxicity.Risk of cytokine release syndrome or neurotoxicity with engineered T cell therapies.
06

Interacting drugs

No approved small-molecule drugs directly target this complex, but multiple T cell receptor (TCR)-based therapeutics, TCR-mimic antibodies, and engineered T cells (including TCR-T and TCRm therapies) are under development targeting PRAME presented by HLA-A*24:02[2][6].
07

Biomarkers

PRAME expression in tumors (for patient selection)[4][6]HLA-A*24:02 positivity in patients (for eligibility to therapies targeting this complex)[6]

Beyond the preview

Go deeper on PRAME peptide-HLA-A*24:02 complex.

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on PRAME peptide-HLA-A*24:02 complex.

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call