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Eur J Pharm Sci ; 102: 35-45, 2017 May 01.
Article in English | MEDLINE | ID: mdl-28188909

ABSTRACT

Infliximab is therapeutic monoclonal antibody (mAb) against TNF-α employed in the treatment of immunoinflammatory diseases. The development of biosimilar mAbs is a global strategy to increase drug accessibility and reduce therapy-associated costs. Herein we compared key physicochemical characteristics and biological activities produced by infliximab and infliximab-Probiomed in order to identify functionally relevant differences between the mAbs. Binding of infliximab-Probiomed to TNF-α was specific and had kinetics comparable to that of the reference product. Both mAbs had highly similar neutralizing efficacy in HUVEC cell cultures stimulated with TNF-α. In vitro induction of CDC and ADCC were also similar between the evaluated products. In vivo comparability was assessed using a transgenic mouse model of arthritis that expresses human TNF-α in a 13-week multiple-administration study. Infliximab and infliximab-Probiomed showed comparable efficacy, safety, and pharmacokinetic profiles. Our results indicate that infliximab-Probiomed has highly similar activities to infliximab in preclinical models, warranting a clinical evaluation of its biosimilarity.


Subject(s)
Antirheumatic Agents , Biosimilar Pharmaceuticals , Infliximab , Animals , Antirheumatic Agents/pharmacokinetics , Antirheumatic Agents/pharmacology , Antirheumatic Agents/therapeutic use , Arthritis/drug therapy , Arthritis/metabolism , Biosimilar Pharmaceuticals/pharmacokinetics , Biosimilar Pharmaceuticals/pharmacology , Biosimilar Pharmaceuticals/therapeutic use , CHO Cells , Cells, Cultured , Cricetulus , Cytokines/genetics , Cytokines/metabolism , E-Selectin/metabolism , HEK293 Cells , Human Umbilical Vein Endothelial Cells/drug effects , Human Umbilical Vein Endothelial Cells/metabolism , Humans , Infliximab/pharmacokinetics , Infliximab/pharmacology , Infliximab/therapeutic use , Intercellular Adhesion Molecule-1/metabolism , Male , Mice , Mice, Transgenic , Vascular Cell Adhesion Molecule-1/metabolism
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