Title of article
Whole-Molecule Antibody Engineering: Generation of a High-Affinity Anti-IL-6 Antibody with Extended Pharmacokinetics
Author/Authors
Donna K. Finch، نويسنده , , Matthew A. Sleeman، نويسنده , , Jacques Moisan، نويسنده , , Franco Ferraro، نويسنده , , Sara Botterell، نويسنده , , Jamie Campbell، نويسنده , , Duncan Cochrane، نويسنده , , Simon Cruwys، نويسنده , , Elizabeth England، نويسنده , , Steven Lane، نويسنده , , Elizabeth Rendall، نويسنده , , Monisha Sinha، نويسنده , , Craig Walker، نويسنده , , Gareth Rees، نويسنده , , Michael A. Bowen، نويسنده , , Amy Schneider، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2011
Pages
17
From page
791
To page
807
Abstract
The differentiation of therapeutic monoclonal antibodies in an increasingly competitive landscape requires optimization of clinical efficacy combined with increased patient convenience. We describe here the generation of MEDI5117, a human anti-interleukin (IL)-6 antibody generated by variable domain engineering, to achieve subpicomolar affinity for IL-6, combined with Fc (fragment crystallizable) engineering to enhance pharmacokinetic half-life. MEDI5117 was shown to be highly potent in disease-relevant cellular assays. The pharmacokinetics of MEDI5117 were evaluated and compared to those of its progenitor, CAT6001, in a single-dose study in cynomolgus monkeys. The antibodies were administered, either subcutaneously or intravenously, as a single dose of 5 mg/kg. The half-life of MEDI5117 was extended by approximately 3-fold, and clearance was reduced by approximately 4-fold when compared to CAT6001. MEDI5117 therefore represents a potential ‘next-generation’ antibody; future studies are planned to determine the potential for affinity-driven efficacy and/or less frequent administration.
Keywords
protein engineering , phage display , combinatorial mutagenesis , Pharmacokinetics , antibody library
Journal title
Journal of Molecular Biology
Serial Year
2011
Journal title
Journal of Molecular Biology
Record number
1254007
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