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

被引:387
作者
Ordas, Ingrid [1 ,2 ]
Mould, Diane R. [3 ]
Feagan, Brian G. [4 ]
Sandborn, William J. [1 ]
机构
[1] Univ Calif San Diego, Div Gastroenterol, La Jolla, CA 92093 USA
[2] Univ Barcelona, Dept Gastroenterol, Hosp Clin Barcelona, CIBER EHD,IDIBAPS, Barcelona, Spain
[3] Project Res Inc, Phoenixville, PA USA
[4] Univ Western Ontario, Robarts Res Inst, London, ON, Canada
关键词
NECROSIS-FACTOR-ALPHA; CERTOLIZUMAB PEGOL CDP870; BRAMBELL RECEPTOR FCRB; CROHNS-DISEASE; ULCERATIVE-COLITIS; CLINICAL-RESPONSE; INFLIXIMAB PHARMACOKINETICS; MAINTENANCE INFLIXIMAB; RHEUMATOID-ARTHRITIS; RANDOMIZED-TRIAL;
D O I
10.1038/clpt.2011.328
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 overtime. 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.
引用
收藏
页码:635 / 646
页数:12
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