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- W1967676683 abstract "At least seven distinct epidermal growth factor (EGF) ligands bind to and activate the EGF receptor (EGFR). This activation plays an important role in the embryo and in the maintenance of adult tissues. Importantly, pharmacologic EGFR inhibition also plays a critical role in the pathophysiology of diverse disease states, especially cancer. The roles of specific EGFR ligands are poorly defined in these disease states. Accumulating evidence suggests a role for transforming growth factor <i>α</i> (TGF<i>α</i>) in skin, lung, and kidney disease. To explore the role of Tgfa, we generated a monoclonal antibody (mAb41) that binds to and neutralizes human Tgfa with high affinity (<i>K</i><sub>D</sub> = 36.5 pM). The antibody also binds human epiregulin (Ereg) (<i>K</i><sub>D</sub> = 346.6 pM) and inhibits ligand induced myofibroblast cell proliferation (IC<sub>50</sub> values of 0.52 and 1.12 nM for human Tgfa and Ereg, respectively). In vivo, a single administration of the antibody to pregnant mice (30 mg/kg s.c. at day 14 after plug) or weekly administration to neonate mice (20 mg/kg s.c. for 4 weeks) phenocopy <i>Tgfa</i> knockout mice with curly whiskers, stunted growth, and expansion of the hypertrophic zone of growth plate cartilage. Humanization of this monoclonal antibody to a human IgG4 antibody (LY3016859) enables clinical development. Importantly, administration of the humanized antibody to cynomolgus monkeys is absent of the skin toxicity observed with current EGFR inhibitors used clinically and no other pathologies were noted, indicating that neutralization of Tgfa could provide a relatively safe profile as it advances in clinical development." @default.
- W1967676683 created "2016-06-24" @default.
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- W1967676683 date "2014-02-11" @default.
- W1967676683 modified "2023-09-26" @default.
- W1967676683 title "Generation and Activity of a Humanized Monoclonal Antibody That Selectively Neutralizes the Epidermal Growth Factor Receptor Ligands Transforming Growth Factor-<i>α</i>and Epiregulin" @default.
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- W1967676683 doi "https://doi.org/10.1124/jpet.113.210765" @default.
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