| Literature DB >> 28188909 |
M A Velasco-Velázquez1, N Salinas-Jazmín2, E Hisaki-Itaya2, L Cobos-Puc2, W Xolalpa2, G González3, A Tenorio-Calvo2, N Piña-Lara3, L C Juárez-Bayardo3, L F Flores-Ortiz3, E Medina-Rivero3, N O Pérez4, S M Pérez-Tapia5.
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.Entities:
Keywords: Biosimilar; Infliximab; Rheumatoid arthritis; TNF-α; Therapeutic mAb; anti-TNF-α
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Year: 2017 PMID: 28188909 DOI: 10.1016/j.ejps.2017.01.038
Source DB: PubMed Journal: Eur J Pharm Sci ISSN: 0928-0987 Impact factor: 4.384