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The anti-B7-H3 humanized monoclonal antibody is a preclinical-stage therapeutic candidate developed by the University of Macau. It specifically targets the Ig-like V1-C1 domains of B7-H3 (CD276), an immune checkpoint molecule overexpressed in various solid tumors, including breast cancer. By binding to B7-H3, the antibody mediates potent antibody-dependent cellular cytotoxicity (ADCC) against triple-negative breast cancer (TNBC) and trastuzumab-resistant HER2-positive breast cancer cells. In preclinical models, including cell-derived xenograft (CDX) and patient-derived xenograft (PDX) mice, the antibody demonstrated significant in vivo anti-tumor activity. Mechanistically, it downregulates the MAPK and NF-kappaB signaling pathways, leading to reduced tumor cell metabolism, migration, inflammation, and cytokine release.
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