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免疫调节剂联合治疗对炎症性肠病患者抗TNF谷浓度及抗体的影响。

Influence of combination therapy with immune modulators on anti-TNF trough levels and antibodies in patients with IBD.

作者信息

van Schaik Tamara, Maljaars Jeroen P W, Roopram Rajiv K, Verwey Marthe H, Ipenburg Nienke, Hardwick James C H, Veenendaal Roeland A, van der Meulen-de Jong Andrea E

机构信息

Department of Gastroenterology, Leiden University Medical Center, Leiden, the Netherlands.

出版信息

Inflamm Bowel Dis. 2014 Dec;20(12):2292-8. doi: 10.1097/MIB.0000000000000208.

Abstract

BACKGROUND

It is important to identify factors that can reduce the incidence of immunogenicity against anti-tumor necrosis factor medication in patients with inflammatory bowel disease. The objective of our study was to evaluate the influence of cotreatment with immune modulators (IMs) on trough levels (TLs) and antidrug antibodies.

METHODS

The records of all patients with inflammatory bowel disease at the Leiden University Medical Center who received either adalimumab or infliximab (IFX) in the year 2011 and/or 2012 (n = 352) were retrospectively evaluated about the assessment of TL and antibodies and use of IM.

RESULTS

Two hundred seventeen patients were included (108 patients IFX; 109 patients adalimumab). Mean TL in the IFX group was higher in the combination therapy group compared with the monotherapy group, 4.6 versus 7.5 µg/mL, P = 0.04. In the adalimumab group, the difference was not significant. In patients with IFX monotherapy, the incidence of antibody formation was higher compared with patients with combination therapy (29.8% versus 5.7%, P = 0.001). IFX patients with a suboptimal dose of IM had a higher TL compared with patients who had an optimal dose, P = 0.02. The incidence of antibody formation was lower in IFX patients who immediately started with IMs compared with patients who did not (33.3% versus 66.7%, P = 0.04).

CONCLUSIONS

The influence of combination therapy with IM on TL and antibodies to anti-tumor necrosis factor medication was significant for IFX-treated patients. Patients who started combination therapy immediately developed antibodies less often than patients who started later with concomitant medication.

摘要

背景

确定可降低炎症性肠病患者对抗肿瘤坏死因子药物免疫原性发生率的因素很重要。我们研究的目的是评估免疫调节剂(IMs)联合治疗对谷浓度(TLs)和抗药物抗体的影响。

方法

回顾性评估2011年和/或2012年在莱顿大学医学中心接受阿达木单抗或英夫利昔单抗(IFX)治疗的所有炎症性肠病患者(n = 352)的TL和抗体评估情况以及IM的使用情况。

结果

纳入217例患者(108例接受IFX治疗;109例接受阿达木单抗治疗)。联合治疗组IFX患者的平均TL高于单药治疗组,分别为4.6 μg/mL和7.5 μg/mL,P = 0.04。在阿达木单抗组,差异不显著。接受IFX单药治疗的患者抗体形成发生率高于联合治疗患者(29.8%对5.7%,P = 0.001)。IM剂量未达最佳的IFX患者的TL高于剂量最佳的患者,P = 0.02。与未立即开始使用IMs的IFX患者相比,立即开始使用IMs的患者抗体形成发生率更低(33.3%对66.7%,P = 0.04)。

结论

IM联合治疗对接受IFX治疗患者的TL和抗抗肿瘤坏死因子药物抗体有显著影响。立即开始联合治疗的患者产生抗体的频率低于较晚开始联合用药的患者。

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