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 ,
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