Anti-TNF-α biotherapies: perspectives for evidence-based personalized medicine

被引:0
|
作者
Bendtzen, Klaus [1 ]
机构
[1] Univ Hosp, Inst Inflammat Res IIR 7521, Rigshosp, DK-2100 Copenhagen, Denmark
关键词
anti-TNF-alpha antibodies; immunogenicity; pharmacodynamics; pharmacokinetics; recombinant protein therapeutics; theranostics; NECROSIS-FACTOR-ALPHA; CHIMERIC MONOCLONAL-ANTIBODY; RHEUMATOID-ARTHRITIS; CLINICAL-RESPONSE; THROMBOEMBOLIC EVENTS; THERAPEUTIC PROTEINS; CROHNS-DISEASE; IMMUNOGENICITY; INFLIXIMAB; ADALIMUMAB;
D O I
10.2217/IMT.12.114
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
This article discusses the rationale behind recommending immunopharmacological guidance of long-term therapies with genetically engineered anti-TNF-alpha immunoglobulin constructs. Arguments why therapeutic decision-making should not rely on clinical outcome alone are presented. Central to this is that the use of theranostics (i.e., monitoring circulating levels of functional anti-TNF-alpha drugs and antidrug antibodies) would markedly improve treatment because therapies can be tailored to individual patients and provide more effective and economical long-term therapies with minimal risk of side effects. Large-scale immunopharmacological knowledge of how patients 'handle' TNF-alpha biopharmaceuticals would also help industry develop more effective and safer TNF-alpha inhibitors.
引用
收藏
页码:1167 / 1179
页数:13
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