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Anti-TNF Monoclonal Antibodies in Inflammatory Bowel Disease: Pharmacokinetics-Based Dosing Paradigms

Clinical Pharmacology & Therapeutics · 2012 · Vol. 91(4) · pp. 635–646
Íngrid OrdásDiane R. MouldB G FeaganWilliam J. Sandborn

Abstract

Crohn's disease and ulcerative colitis are chronic inflammatory disorders resulting from immune dysregulation. Patients who fail conventional medical therapy require biological treatment with monoclonal antibodies (mAbs). Although mAbs are highly effective for induction and maintenance of clinical remission, not all patients respond, and a high proportion of patients lose response over time. One factor associated with loss of response is immunogenicity, whereby the production of antidrug antibodies accelerates mAb clearance. However, other factors related to patient and disease characteristics also influence the pharmacokinetics of mAbs. These factors include gender, body size, concomitant use of immunosuppressive agents, disease type, serum albumin concentration, and the degree of systemic inflammation. Because it is important to maintain clinically effective concentrations to provide optimal clinical response and drug exposure is affected by patient factors, a better understanding of the pharmacology of mAbs will ultimately result in better patient care.

Inflammatory Bowel DiseaseMonoclonal and Polyclonal Antibodies ResearchBiosimilars and Bioanalytical MethodsMedicineUlcerative colitisMonoclonal antibodyInflammatory bowel diseasePharmacokineticsImmunogenicityImmunologyCrohn's diseaseDosingImmune system

MeSH terms

InfliximabAnimalsAntibodies, MonoclonalDose-Response Relationship, ImmunologicDrug Therapy, CombinationHumansTumor Necrosis Factor-alphaInflammatory Bowel DiseasesAntibodies, Monoclonal, Humanized
Citations
502
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30.81
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70
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Cited by
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