药代动力学
抗体
单克隆抗体
药理学
蛋白质工程
化学
医学
免疫学
生物化学
酶
作者
Donna K. Finch,Matthew A. Sleeman,Jacques Moisan,Franco Ferraro,Sara Botterell,Jamie I. D. Campbell,Duncan Cochrane,Simon Cruwys,Elizabeth England,Steven Lane,E Rendall,Monisha Sinha,Craig Walker,Gareth Rees,Michael A. Bowen,Amy Schneider,Meina Liang,Raffaella Faggioni,Michael Fung,Philip R. Mallinder
标识
DOI:10.1016/j.jmb.2011.06.031
摘要
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.
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