Target intelligence / Profile preview

Integrin subunit alpha D (ITGAD)

Target
ITGAD
Molecular classification
Integrin, Cell adhesion molecule, Receptor, Membrane glycoprotein
01

Overview

Integrin subunit alpha D (ITGAD), also known as CD11d, is a member of the beta-2 integrin family of membrane glycoproteins. It partners with the common β2 chain (CD18) to form the αDβ2 integrin receptor, which is predominantly expressed on myeloid lineage cells such as monocytes, macrophages, dendritic cells, and polymorphonuclear leukocytes[1][2][4]. Integrin αDβ2 mediates cell adhesion and migration by binding to cell surface ligands including ICAM-3 and VCAM-1, and is involved in outside-in signaling that promotes inflammatory gene expression and chemokine/cytokine production. It plays key roles in modulating innate immune responses, particularly in chronic inflammation, and contributes to macrophage fusion in inflammatory environments[1][6]. While ITGAD is recognized as a valid immunological and potential therapeutic target, it is not currently targeted by any approved drugs.

Other names
CD11dADB2integrin alpha-Dleukointegrin alpha Dintegrin αDCD11 antigen-like family member Dbeta-2 integrin alphaD subunitItgax
02

Mechanism of action

Inhibitors (when developed) would block cell adhesion and migration via integrin αDβ2, attenuating immune cell infiltration and inflammatory processes[6].

03

Biological functions

Leukocyte adhesionImmune response modulationCell migrationSignal transductionMacrophage fusion
04

Disease associations

InflammationAtherosclerosisChronic inflammatory conditions
05

Safety considerations

Targeting β2 integrins broadly may suppress immune cell adhesion and migration, increasing the risk of infection or impairing tissue repair[1][6]. Specific safety profiles for ITGAD inhibition remain to be determined.
06

Interacting drugs

No approved drugs directly or selectively targeting integrin subunit alpha D (ITGAD) are currently listed in the public domain[6]. Some pan-integrin or β2 integrin inhibitors may potentially affect ITGAD function.
07

Biomarkers

Increased ITGAD expression may serve as a biomarker in activated myeloid cells during inflammatory conditions and tissue infiltration, but no established, clinical biomarker applications currently exist[1][4].

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