The standard of care for patients with HER2-positive cancers is well established, but a significant unmet need exists for patients with HER2-low tumors, who do not meet the eligibility criteria for trastuzumab, and for patients with HER2-positive tumors, who are refractory to trastuzumab treatment. Therefore, in this study, we developed a NANOBODY domain-based HER2-targeting, T-cell receptor αβ-based T-cell engager (TCE) molecule-TPP-45142; it recognizes a HER2 epitope distinct from that recognized by trastuzumab and pertuzumab and redirects T cells to kill HER2-low cancers such as breast, gastric, and gastroesophageal junction adenocarcinoma cancers. TPP-45142 mediated potent T cell-dependent cytotoxicity against HER2-low cancer cell lines in vitro and inhibited in vivo tumor growth of HER2-low breast cancer xenografts. TPP-45142 was highly selective toward tumor cells expressing low HER2 levels than toward normal cardiac cells and exhibited a favorable therapeutic index as per a cytokine release assay. Thus, TPP-45142, with an improved safety profile, is a promising next-generation TCE for treating challenging HER2-low cancers.
TPP-45142-an Anti-HER2 T-cell Engager-Designed for Selective HER2-Low Cancer Immunotherapy.
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作者:De Tavernier Evelyn, Kim Peter S, Bruch Eduardo M, Cortez-Retamozo Virna F, Timmerman Lien, Flynn Alyssa L, Van Overbeke Wouter, Tirode Fabrice, Cintra Barbosa-Lorenzi Valeria, Piepenhagen Peter, Dinh-Le Thuvan, Luna Ernesto, Li Aiqun, Baker Ann, Rak Alexey, Pao Lily I, Vintém Ana Paula B
| 期刊: | Molecular Cancer Therapeutics | 影响因子: | 5.500 |
| 时间: | 2026 | 起止号: | 2026 Apr 2; 25(4):541-555 |
| doi: | 10.1158/1535-7163.MCT-25-0654 | ||
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