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在炎症性肠病患者中添加免疫调节剂可抑制对英夫利昔单抗或阿达木单抗的抗药抗体。

Suppression of anti-drug antibodies to infliximab or adalimumab with the addition of an immunomodulator in patients with inflammatory bowel disease.

作者信息

Strik A S, van den Brink G R, Ponsioen C, Mathot R, Löwenberg M, D'Haens G R

机构信息

Department of Gastroenterology, Academic Medical Centre Amsterdam, Amsterdam, the Netherlands.

Department Hospital Pharmacy, Academic Medical Centre Amsterdam, Amsterdam, the Netherlands.

出版信息

Aliment Pharmacol Ther. 2017 Apr;45(8):1128-1134. doi: 10.1111/apt.13994. Epub 2017 Feb 23.

Abstract

BACKGROUND

Loss of response to anti-tumour necrosis factor (TNF) therapy in patients with inflammatory bowel disease (IBD) is often caused by anti-drug antibody formation with neutralisation of drug effect. Addition of an immunomodulator has been suggested to reduce immunogenicity, leading to regained response.

AIM

To investigate whether addition of an immunomodulator to anti-TNF monotherapy could lead to anti-drug antibody suppression and regained clinical response in IBD patients.

METHODS

We retrospectively collected measurements of infliximab or adalimumab serum concentrations and anti-drug antibodies to identify anti-drug positive patients with loss response who were given an immunomodulator.

RESULTS

Anti-drug antibodies against infliximab and adalimumab were detected in 98/376 (26%) and in 61/226 (27%) patients, respectively. Immunomodulators were given to 17/159 patients. Clinical response was recaptured in 6/10 patients receiving a thiopurine and in all (7/7) patients receiving methotrexate. In 7/8 patients on infliximab, serum concentrations increased (median 2.84 μg/mL; IQR: 1.19-4.98) and in 6/9 patients on adalimumab (median 3.10 μg/mL; IQR: 1.45-4.45). This was accompanied by a decrease in anti-drug antibodies to undetectable levels (median 11 months for both anti-TNF agents). In 23 patients, no immunomodulator was added but anti-TNF interval was shortened (17/23) or dosage was increased (6/23), which resulted in a clinical response in 10/17 and 2/6 patients, respectively.

CONCLUSION

In 77% of IBD patients with loss of response due to immunogenicity, addition of immunomodulator resulted in undetectable anti-drug antibody levels, increased serum drug concentrations and regained clinical response. This strategy should be considered in this patient population before switching to other agents.

摘要

背景

炎症性肠病(IBD)患者对抗肿瘤坏死因子(TNF)治疗失去反应通常是由于抗药抗体形成导致药物效应中和。有人提出添加免疫调节剂以降低免疫原性,从而恢复反应。

目的

研究在IBD患者中,在抗TNF单药治疗基础上添加免疫调节剂是否能抑制抗药抗体并恢复临床反应。

方法

我们回顾性收集了英夫利昔单抗或阿达木单抗血清浓度及抗药抗体的检测结果,以确定对失去反应的抗药抗体阳性患者给予免疫调节剂。

结果

分别在98/376(26%)和61/226(27%)的患者中检测到了针对英夫利昔单抗和阿达木单抗的抗药抗体。17/159例患者接受了免疫调节剂治疗。接受硫唑嘌呤的10例患者中有6例恢复了临床反应,接受甲氨蝶呤的所有7例患者均恢复了临床反应。在接受英夫利昔单抗治疗的8例患者中的7例中,血清浓度升高(中位数2.84μg/mL;四分位间距:1.19 - 4.98),在接受阿达木单抗治疗的9例患者中的6例中(中位数3.10μg/mL;四分位间距:1.45 - 4.45)。同时抗药抗体降至检测不到的水平(两种抗TNF药物均为中位数11个月)。23例患者未添加免疫调节剂,但缩短了抗TNF治疗间隔(17/23)或增加了剂量(6/23),分别使10/17和2/6的患者产生了临床反应。

结论

在77%因免疫原性而失去反应的IBD患者中,添加免疫调节剂可使抗药抗体水平降至检测不到,血清药物浓度升高,并恢复临床反应。在该患者群体转向其他药物治疗之前,应考虑这一策略。

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