Protein / target
Integrin beta-7
Protein at a glance
Biological role
Cell adhesion molecule binding
Strongest disease association
Crohn's Disease
Therapeutic position
Established drug target
Derived from structured UniProt, Open Targets and literature data on this page.
Protein profile
Canonical identity and biological annotation from UniProt.
Function overview
Integrin ITGA4/ITGB7 (alpha-4/beta-7) (Peyer patches-specific homing receptor LPAM-1) is an adhesion molecule that mediates lymphocyte migration and homing to gut-associated lymphoid tissue (GALT) (Probable).
View complete UniProt function annotationHide complete annotation
Integrin ITGA4/ITGB7 (alpha-4/beta-7) (Peyer patches-specific homing receptor LPAM-1) is an adhesion molecule that mediates lymphocyte migration and homing to gut-associated lymphoid tissue (GALT) (Probable). Integrin ITGA4/ITGB7 interacts with the cell surface adhesion molecules MADCAM1 which is normally expressed by the vascular endothelium of the gastrointestinal tract (PubMed:10837471, PubMed:14608374). Also interacts with VCAM1 and fibronectin, an extracellular matrix component (Probable). It recognizes one or more domains within the alternatively spliced CS-1 region of fibronectin (Probable). Interactions involve the tripeptide L-D-T in MADCAM1, and L-D-V in fibronectin (Probable). Integrin ITGAE/ITGB7 (alpha-E/beta-7, HML-1) is a receptor for E-cadherin (PubMed:10837471)
Subcellular location
Domains and Gene Ontology detail (30)Hide
Domains & features
Gene Ontology
- Ccell surface
- Cextracellular exosome
- Cfocal adhesion
- Cintegrin alpha4-beta7 complex
- Cintegrin complex
- Cmembrane
- Cplasma membrane
- Creceptor complex
- Fcell adhesion molecule binding
- Fintegrin binding
- Fmetal ion binding
- Fvirus receptor activity
Biological roles
What this protein does, drawn together from its UniProt function, Gene Ontology terms and Reactome pathways.
View supporting evidenceHide supporting evidence
Cell migration
- ·cell-matrix adhesion involved in ameboidal cell migration
Cell adhesion
- ·Integrin ITGA4/ITGB7 (alpha-4/beta-7) (Peyer patches-specific homing receptor LPAM-1) is…
- ·cell adhesion molecule binding
- ·cell adhesion
- ·cell adhesion mediated by integrin
Immune signalling
- ·immune response in gut-associated lymphoid tissue
- ·substrate adhesion-dependent cell spreading
Concepts derived from UniProt GO Reactome — each badge above shows which sources supported that role.
Approved medicines with mapped indications
Approved therapies targeting this protein, grouped by what they are approved to treat — the disease-first view of the medicines below. Relationships come from the canonical approved-indication graph (ChEMBL phase-4), the same source as the drug cards.
Approved indications from ChEMBL (phase-4), via the canonical drug→disease graph.
Drugs targeting this protein
How approved and investigational drugs engage this protein — mechanism and action type, direct vs complex targeting, and how broadly each acts across other targets. A drug-first view (the section above groups the approved ones disease-first); direct binders with few recorded targets are listed first.
Integrin alpha-4/beta-7 inhibitor
Indicated for Crohn's Disease, Inflammation, Multiple Sclerosis, Multiple Sclerosis, Relapsing-Remitting
Integrin alpha-4/beta-7 inhibitor
Indicated for Colitis, Ulcerative, Crohn's Disease
ChEMBL mechanism, action type, target identity and approved indications. Open Targets clinical status.
Translational evidence
Why this target matters therapeutically, strongest evidence first. Disease associations are gene-level (via the gene that encodes this protein) and open into the full confidence synthesis; the development universe, tractability and safety annotations are target-level, from Open Targets.
Strongest disease associations · via encoding gene ITGB7
Gene-level evidence surfaced through the gene ITGB7 that encodes this protein — not a direct protein–disease relationship. Ranked by Forefront's causal-directness weighting, so genetically- and clinically-evidenced diseases lead over ones that merely share the literature.
View evidence synthesis (4)Hide
The evidence agreement range shows how closely the independent evidence families agree — it is not a statistical confidence interval, and nothing here is fitted to outcome data. Derived from Open Targets evidence types under Forefront weighting; the per-type scores above show the calculation.
Show all associationsHide all associations
Drug development
5 compounds recorded · 2 approved · 3 in clinical development
View all recorded compounds (5)Hide
Open Targets known-drugs universe. Drug name and highest clinical stage only — the disease relationship is NOT read from this slice (it carries trial-context noise); approved indications come from the canonical graph above.
Tractability
Small molecules — Strong
Antibodies — Strong
Protein degraders — Emerging
View underlying tractability evidence (11)Hide
Raw Open Targets tractability assessment buckets, by modality.
Clinical trials
Trials of drugs that target this protein — reached indirectly through those drugs, so a trial listed here studies the drug, not the protein. Ranked by active status, then clinical phase and recency, and spread across the targeting drugs.
View all trials (26)Hide
ClinicalTrials.gov via the drug-target graph.
What's happening now
Recent therapeutic activity around this target — regulatory actions, clinical trials and safety signals for 2 drugs that target this protein, plus publications where such a drug is a genuine subject. Every item is reached indirectly through the drug, not the protein itself; incidental mentions (a paper that merely measures a drug) and press items are excluded.
- Supplemental approval
Supplemental approval: NATALIZUMAB-SZTN (BLA761322)
- Supplemental approval
Supplemental approval: NATALIZUMAB-SZTN (BLA761322)
- Label change
Label change: NATALIZUMAB-SZTN (BLA761322)
- Regulatory approval
Approval: Tyruko (EMA)
- Regulatory approval
Approval: NATALIZUMAB-SZTN (BLA761322)
- New publicationVedolizumab in Japanese patients with ulcerative colitis: A Phase 3, randomized, double-blind, placebo-controlled study.
- Safety communication
Drug Safety Update: Natalizumab (Tysabri▼): progressive multifocal leukoencephalopathy—updated advice to support early detection
- Safety communication
Drug Safety Update: Natalizumab (Tysabri▼): risk of progressive multifocal leukoencephalopathy increases after 2 years of therapy
- Safety communication
Drug Safety Update: Natalizumab (Tysabri▼): risk of progressive multifocal leukoencephalopathy is increased in patients who have had previous immunosuppressant treatment
- Regulatory approval
Approval: Entyvio (EMA)
- New publicationVedolizumab as induction and maintenance therapy for ulcerative colitis.
- Regulatory approval
Approval: Tysabri (EMA)
Objective event titles are shown unmodified; the event kind and significance line are derived from structured fields. Forefront AttentionEvent stream aggregating Europe PMC Regulatory filings ClinicalTrials.gov.