Wolbink Gerrit J, Aarden Lucien A, Dijkmans B A C
Department of Rheumatology, Jan van Breemen Institute, Dr Jan van Breemenstraat 2, Amsterdam 1056 AB, The Netherlands.
Curr Opin Rheumatol. 2009 May;21(3):211-5. doi: 10.1097/bor.0b013e328329ed8b.
In the last decade, biologicals revolutionized rheumatology. An increasing number of patients benefit from biotherapeuticals. However, some patients do not respond to treatment and others lose their response after a certain time. Immunogenicity is one of the factors linked to secondary nonresponse but its clinical significance has remained controversial.
In recent years, knowledge of how to assess immunogenicity of biologicals has improved. Various reports show an inverse relationship between drug levels and antibody formation against the drug. Studies associated immunogenicity of therapeutic antibodies with clinically significant nonresponse in a subgroup of patients. Clinically relevant immunogenicity is influenced by several factors including dosing and concomitant medication. It has been shown that immunogenicity against biologicals can be persistent or transient.
Immunogenicity affects a significant number of patients treated with biologicals. Monitoring of drug levels as well as of antibodies against therapeutic antibodies may lead to more rational treatment strategies.
在过去十年中,生物制剂给风湿病学带来了革命性变化。越来越多的患者从生物治疗中获益。然而,一些患者对治疗无反应,另一些患者在一段时间后失去反应。免疫原性是与继发性无反应相关的因素之一,但其临床意义仍存在争议。
近年来,评估生物制剂免疫原性的知识有所改进。各种报告显示药物水平与针对该药物的抗体形成之间存在反比关系。研究表明,治疗性抗体的免疫原性与一部分患者临床上显著的无反应有关。临床相关的免疫原性受多种因素影响,包括给药剂量和联合用药。已表明,针对生物制剂的免疫原性可以是持续性的或短暂性的。
免疫原性影响大量接受生物制剂治疗的患者。监测药物水平以及针对治疗性抗体的抗体可能会带来更合理的治疗策略。