Target intelligence / Profile preview

Immature laminin receptor protein (iLRP) (iLRP)

Target
iLRP
Molecular classification
Ribosomal protein, Tumor-associated antigen, Cell adhesion molecule
01

Overview

The immature laminin receptor protein (iLRP), also known as oncofetal antigen (OFA), is a 37 kDa protein that serves as the precursor to the 67 kDa laminin receptor (UniProt P08865). It is encoded by the RPSA gene and plays a critical role in ribosome assembly and cell-extracellular matrix interactions (PubMed: 12885710). While expressed during fetal development, iLRP is largely absent in normal adult tissues but is highly overexpressed in a variety of cancers, including leukemias and solid tumors (PubMed: 16424169). This differential expression pattern identifies it as a universal tumor-associated antigen (TAA) suitable for targeted immunotherapy (PubMed: 15934656). In clinical applications, autologous dendritic cells are pulsed with OFA/iLRP to present its epitopes via MHC class I molecules to CD8+ T cells (PubMed: 12885710). This presentation triggers the activation of cytotoxic T lymphocytes that specifically recognize and destroy tumor cells expressing the antigen. Therapeutic strategies targeting OFA/iLRP have been investigated in clinical trials for patients with acute myeloid leukemia and other malignancies (ClinicalTrials.gov: NCT00101166). The use of dendritic cells as a delivery vehicle helps to overcome the immunosuppressive environment often found in advanced cancers. Monitoring for efficacy typically involves measuring the expansion of OFA/iLRP-specific T cells and tumor regression. Safety concerns primarily involve the potential for low-level expression in normal tissues to trigger autoimmune responses, although clinical data suggests a high degree of tumor specificity.

Other names
Oncofetal antigenOFA/iLRP37 kDa laminin receptor precursorRPSARibosomal protein SA67 kDa laminin receptor precursor
02

Mechanism of action

Induction of a cytotoxic T-lymphocyte (CTL) response through the presentation of OFA/iLRP-derived peptides on MHC class I molecules by dendritic cells to CD8+ T cells.

03

Biological functions

Cell adhesionProtein synthesisImmune responseSignal transduction
04

Disease associations

CancerLeukemiaLymphomaBreast cancerLung cancerColon cancer
05

Safety considerations

Potential for autoimmune reactions against normal tissues expressing low levels of iLRPTumor immune evasion via MHC downregulation
06

Interacting drugs

OFA-iLRP-pulsed dendritic cell vaccine
07

Biomarkers

OFA/iLRP surface expressionHLA-A2 statusCD8+ T-cell activationInterferon-gamma production

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