Target intelligence / Profile preview

Cluster of Differentiation 276 (B7 homolog 3) (B7-H3 (CD276))

Target
B7-H3 (CD276)
Molecular classification
Type I transmembrane protein, Immune checkpoint molecule, Member of B7 family, Receptor ligand (typically grouped with receptors in therapeutic target databases), Tumor endothelial marker
01

Overview

Cluster of Differentiation 276 (B7 homolog 3; B7-H3; CD276) is a 316-amino-acid type I transmembrane protein belonging to the B7 family of immune checkpoint molecules. It exists in two major isoforms, 2IgB7-H3 and 4IgB7-H3, based on the number of extracellular immunoglobulin-like domains; the 4Ig form predominates in humans and especially in cancer tissue. B7-H3 is encoded by the CD276 gene on human chromosome 15. Physiologically, it functions as a negative regulator in adaptive immunity, suppressing T cell activation. In cancer, B7-H3 acts as a key immune checkpoint ligand inhibiting tumor antigen-specific immune responses, supporting tumor cell proliferation, migration, invasion, angiogenesis, and resistance to therapy. Its high expression in a broad range of tumors and limited normal tissue expression have made it an attractive target for antibody-based therapies, CAR T cell therapies, and other immunotherapy modalities. Several agents targeting B7-H3 are in clinical development, and B7-H3 expression serves as a biomarker for patient selection and monitoring efficacy. Notable safety concerns include possible off-tumor toxicities and incomplete understanding of its full physiological roles.

Other names
B7-H3CD276Cluster of Differentiation 276B7 homolog 3
02

Mechanism of action

Antibody-dependent cell-mediated cytotoxicity (ADCC); Immune checkpoint blockade (enhancing antitumor T cell activity); Direct cytotoxicity via drug conjugates; CAR T cell-mediated tumor cell lysis; Disruption of B7-H3 ligand-mediated tumor-promoting signals

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Biological functions

Immune response regulation (costimulatory/coinhibitory)Suppression of T cell activation and proliferation in non-malignant tissuesTumor antigen-specific immune response inhibition (checkpoint ligand function)Promotion of tumor cell proliferation, migration, invasion, angiogenesis, chemoresistance, epithelial-to-mesenchymal transition (EMT), and altered metabolismInduction of anti-apoptosisCell-cell signaling
04

Disease associations

Cancer (highly expressed in many solid tumors, associated with poor prognosis)Inflammation (minor role, less established)Potential roles in other diseases remain under investigation
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Safety considerations

Off-tumor/on-target toxicity due to activation of immune responses in non-tumor tissues (though normal adult tissue expression is low)Cytokine release syndrome (CRS) with some immune therapiesPotential impact on physiological angiogenesis and tissue homeostasisLimited understanding of all B7-H3 normal functions, raising theoretical risk for unexpected side effects
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Interacting drugs

Enoblituzumab (MGA271)

6 more in the full profile.

07

Biomarkers

B7-H3 protein expression (for patient selection and efficacy monitoring in cancer therapies)Tumor cell and tumor-associated endothelial B7-H3 expression profiles

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