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Development of XPA067.06, a potent high affinity human anti-gastrin monoclonal antibody.
Hsu, Ssucheng J; Patel, Amita; Larsen, Paul D; Bohmann, David J; Bauer, Robert J; Ma, Jeremy K; Masat, Linda; Roell, Marina; Babuka, Susan J; Hansen, Rhonda K; White, Mark; Haak-Frendscho, Mary.
Afiliación
  • Hsu SJ; Preclinical Research & Development, XOMA (US) LLC, 2910 Seventh Street, Berkeley, CA 94710, USA. hsu@xoma.com
Biochem Pharmacol ; 76(3): 340-52, 2008 Aug 01.
Article en En | MEDLINE | ID: mdl-18589401
The peptide hormone gastrin is a key factor in regulation of gastric acid secretion. It has also been implicated in the development or maintenance of various types of cancer, such as pancreatic and stomach carcinoma. Inhibition of gastrin activity has potential for therapeutic use as a suppressor of acid secretion as well as an inhibitor of gastrin-responsive tumors. XPA067.06 is an affinity matured, 30 pM fully human anti-gastrin monoclonal antibody that was generated. The antibody was tested in a mouse gastric pH model to determine its effect on acid secretion. In this model, animals were treated with human gastrin, XPA067.06, and H2R or M1 receptor antagonists. Gastric fluid was collected and acid output was measured as a function of pH. XPA067.06 was shown to significantly inhibit gastrin-17-stimulated acid output for at least 48h. These results demonstrate that XPA067.06 effectively binds and neutralizes human gastrin-17 in vivo with rapid onset and prolonged duration of efficacy.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Gastrinas / Anticuerpos Monoclonales / Afinidad de Anticuerpos Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Biochem Pharmacol Año: 2008 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Gastrinas / Anticuerpos Monoclonales / Afinidad de Anticuerpos Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Biochem Pharmacol Año: 2008 Tipo del documento: Article País de afiliación: Estados Unidos