Target intelligence / Profile preview

Integrin alpha E (CD103)

Target
CD103
Molecular classification
Integrin, Receptor, Cell adhesion molecule, Type I membrane protein
01

Overview

Integrin alpha E (CD103) is a type I transmembrane protein that forms a heterodimer with the integrin beta 7 subunit (nih.gov). It is primarily expressed on intraepithelial lymphocytes (IELs), tissue-resident memory T (Trm) cells, and specific subsets of dendritic cells, particularly in mucosal tissues such as the gut, lungs, and skin (mdpi.com). Its primary biological function is to mediate cell adhesion and the retention of lymphocytes within epithelial tissues by binding to its ligand, E-cadherin (nih.gov). In oncology, CD103 is a critical marker for tumor-infiltrating lymphocytes (TILs), where its presence often correlates with improved prognosis and better responses to immune checkpoint inhibitors (nih.gov). In inflammatory diseases like ulcerative colitis and Crohn's disease, CD103-mediated retention of pathogenic T cells contributes to chronic inflammation, making it a target for therapeutic intervention (oup.com). Drugs like etrolizumab target the beta 7 subunit to block both alpha 4 beta 7 and alpha E beta 7 (CD103) interactions, aiming to reduce leukocyte infiltration and retention in the intestinal mucosa (mdpi.com). Additionally, novel cell therapies like AGX-148 utilize CD103 as a biomarker to select for tumor-reactive T cells (agonox.com).

Other names
ITGAEHML-1Integrin alpha-EMucosal lymphocyte 1 antigenCD103 antigenIntegrin subunit alpha E
02

Mechanism of action

Inhibition of lymphocyte homing and retention in mucosal tissues by blocking the interaction between the alpha E beta 7 integrin and E-cadherin (mdpi.com).

03

Biological functions

Cell adhesionLymphocyte homingLymphocyte retentionImmune responseT cell activationCytotoxicity
04

Disease associations

CancerInflammationInflammatory bowel diseaseInfectionAutoimmune disease
05

Safety considerations

Increased risk of enteric infectionsPotential for systemic immune-related adverse eventsTherapeutic challenge in balancing effector T cell depletion with regulatory T cell function
06

Interacting drugs

Etrolizumab

1 more in the full profile.

07

Biomarkers

CD103+ tumor-infiltrating lymphocytesCD103+ CD39+ tumor-reactive T cellsIntratumoral ITGAE expression

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