Coenen Marieke J H, Toonen Erik J M, Scheffer Hans, Radstake Timothy R D J, Barrera Pilar, Franke Barbara
Radboud University, Nijmegen Medical Centre, Department of Human Genetics, Internal Mail 855, PO Box 9101, 6500 HB, Nijmegen, The Netherlands.
Pharmacogenomics. 2007 Jul;8(7):761-73. doi: 10.2217/14622416.8.7.761.
TNF-blocking strategies are widely used in the treatment of rheumatoid arthritis (RA). Three anti-TNF agents are registered for use in RA: etanercept, infliximab and adalimumab. Although anti-TNF therapy is very effective in controlling disease activity and slowing down radiological damage, prolonged response is only seen in approximately 70% of the patients. The causes for nonresponse in the remaining patients have not yet been elucidated. Pharmacogenetic studies focusing on genes involved in RA etiology (and/or progression) and in the pharmacokinetics of TNF-blocking agents have identified markers associated with anti-TNF treatment outcome. In the future, more exhaustive, less hypothesis-driven search strategies are expected to discover additional markers. Identification of these markers might be viewed as the first step towards tailored TNF-blocking therapy for patients with RA. Nevertheless, replication and large prospective studies will be needed to demonstrate the validity of the identified genetic markers before implementation into daily clinical practice.
肿瘤坏死因子(TNF)阻断策略广泛应用于类风湿关节炎(RA)的治疗。有三种抗TNF药物已获批用于治疗RA:依那西普、英夫利昔单抗和阿达木单抗。尽管抗TNF治疗在控制疾病活动和减缓放射学损伤方面非常有效,但只有约70%的患者能获得持久缓解。其余患者无反应的原因尚未阐明。针对参与RA病因(和/或进展)以及TNF阻断剂药代动力学的基因进行的药物遗传学研究,已确定了与抗TNF治疗结果相关的标志物。未来,预计采用更详尽、较少基于假设的搜索策略会发现更多标志物。这些标志物的识别可被视为朝着为RA患者量身定制TNF阻断治疗迈出的第一步。然而,在将其应用于日常临床实践之前,还需要进行重复验证和大型前瞻性研究,以证明所识别的基因标志物的有效性。