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Brain penetration, target engagement, and disposition of the blood-brain barrier-crossing bispecific antibody antagonist of metabotropic glutamate receptor type 1.
Webster, Carl I; Caram-Salas, Nadia; Haqqani, Arsalan S; Thom, George; Brown, Lee; Rennie, Kerry; Yogi, Alvaro; Costain, Willard; Brunette, Eric; Stanimirovic, Danica B.
Afiliação
  • Webster CI; Antibody Discovery and Protein Engineering, MedImmune, Cambridge, United Kingdom; websterc@medimmune.com.
  • Caram-Salas N; Human Health Therapeutics Portfolio, National Research Council of Canada, Ottawa, Ontario, Canada.
  • Haqqani AS; Human Health Therapeutics Portfolio, National Research Council of Canada, Ottawa, Ontario, Canada.
  • Thom G; Antibody Discovery and Protein Engineering, MedImmune, Cambridge, United Kingdom;
  • Brown L; Translational Sciences, MedImmune, Cambridge, United Kingdom; and.
  • Rennie K; Human Health Therapeutics Portfolio, National Research Council of Canada, Ottawa, Ontario, Canada.
  • Yogi A; Human Health Therapeutics Portfolio, National Research Council of Canada, Ottawa, Ontario, Canada.
  • Costain W; Human Health Therapeutics Portfolio, National Research Council of Canada, Ottawa, Ontario, Canada.
  • Brunette E; Human Health Therapeutics Portfolio, National Research Council of Canada, Ottawa, Ontario, Canada.
  • Stanimirovic DB; Human Health Therapeutics Portfolio, National Research Council of Canada, Ottawa, Ontario, Canada.
FASEB J ; 30(5): 1927-40, 2016 05.
Article em En | MEDLINE | ID: mdl-26839377
Receptor mediated transcytosis harnessing the cellular uptake and transport of natural ligands across the blood-brain barrier (BBB) has been identified as a means for antibody delivery to the CNS. In this study, we characterized bispecific antibodies in which a BBB-crossing antibody fragment FC5 was used as a BBB carrier. Cargo antibodies were either a high-affinity, selective antibody antagonist of the metabotropic glutamate receptor-1 (BBB-mGluR1), a widely abundant CNS target, or an IgG that does not bind the CNS target (BBB-NiP). Both BBB-NiP and BBB-mGluR1 demonstrated a similar 20-fold enhanced rate of transcytosis across an in vitro BBB model compared with mGluR1 IgG fused to a control antibody fragment. All 3 bispecific antibodies exhibited identical pharmacokinetics in vivo Comparative assessment of BBB-NiP and BBB-mGluR1 revealed that, whereas their serum pharmacokinetics and BBB penetration were identical, their central disposition (brain levels) and elimination (cerebrospinal fluid levels) were widely different, due to central target-mediated removal of the mGluR1-engaging antibody. Central mGluR1 target engagement after systemic administration was demonstrated by a dose-dependent inhibition of mGluR-1-mediated thermal hyperalgesia and by colocalization of the antibody with thalamic neurons involved in mGluR1-mediated pain processing. We demonstrate the feasibility of targeting central G-protein-coupled receptors using a BBB-crossing bispecific antibody approach and emerging principles that govern brain distribution and disposition of these antibodies. These data will be important for designing safe and selective CNS antibody therapeutics.-Webster, C. I., Caram-Salas, N., Haqqani, A. S., Thom, G., Brown, L., Rennie, K., Yogi, A., Costain, W., Brunette, E., Stanimirovic, D. B. Brain penetration, target engagement, and disposition of the blood-brain barrier-crossing bispecific antibody antagonist of metabotropic glutamate receptor type 1.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dor / Encéfalo / Receptores de Glutamato Metabotrópico / Anticorpos Biespecíficos Tipo de estudo: Etiology_studies Limite: Animals / Humans Idioma: En Revista: FASEB J Assunto da revista: BIOLOGIA / FISIOLOGIA Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dor / Encéfalo / Receptores de Glutamato Metabotrópico / Anticorpos Biespecíficos Tipo de estudo: Etiology_studies Limite: Animals / Humans Idioma: En Revista: FASEB J Assunto da revista: BIOLOGIA / FISIOLOGIA Ano de publicação: 2016 Tipo de documento: Article