| Literature DB >> 27737604 |
Roger A Levy1, Renato Guzman2, Gilberto Castañeda-Hernández3, Manuel Martinez-Vazquez4, Guilherme Damian5, Carlos Cara6.
Abstract
Biologics are increasingly being used to modify the course of immune-mediated inflammatory diseases. Some main agents are monoclonal antibodies and a fusion-protein that target TNF. This group includes adalimumab, infliximab, certolizumab pegol, golimumab and etanercept. Although the efficacy of anti-TNFs is supported by numerous randomized clinical trials, their pharmacokinetics depend on many factors, in particular immunogenicity, which can cause marked and rapid clearance and a consequent decrease in efficacy. Kinetics involve receptors that recognize the Fc fragment of the antibody and are responsible for various processes. Pharmacological advances permit optimizing the pharmacokinetics of anti-TNFs. In this review, we examine the kinetics of anti-TNF biologics, and consequent therapeutic implications, and overview some latest developments in the field. First draftsubmitted: 17 May 2016; Accepted for publication: 15 September2016; Published online: 14 October 2016.Entities:
Keywords: Fc receptor γ immunogenicity; anti-TNF; immune-mediated inflammatory diseases; monoclonal antibodies; pharmacokinetics
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Year: 2016 PMID: 27737604 DOI: 10.2217/imt-2016-0067
Source DB: PubMed Journal: Immunotherapy ISSN: 1750-743X Impact factor: 4.196