Division of Internal Medicine, Department of Inflammatory Bowel Disease, Hyogo College of Medicine, Hyogo, Japan.
Dojima Internal Medicine and Gastroenterological Clinic, Osaka, Japan.
J Crohns Colitis. 2020 Sep 16;14(9):1264-1273. doi: 10.1093/ecco-jcc/jjaa051.
In inflammatory bowel disease [IBD] patients, antibody-to-infliximab [ATI] generation is responsible for loss of response [LOR] and infusion reaction [IR] to infliximab. An immuno-therapeutic approach is considered an option to overcome LOR. Granulocyte/monocyte adsorptive apheresis [GMA] using an Adacolumn has been shown to have clinical efficacy together with immunomodulatory effects in IBD patients.
We developed an ATI-CAI assay utilizing a C1q immobilized plate and applied it to measure ATI in patients who were receiving infliximab, including 56 with sustained response, 76 with LOR and six with IR. Furthermore, 14 patients with LOR and two with paradoxical skin reactions who received infliximab + GMA combination therapy were analysed.
Fourteen patients with LOR, seven with Crohn's disease and seven with ulcerative colitis, showed significantly improved clinical indices [p = 0.0009], and decreased ATI [p = 0.0171] and interleukin-6 [p = 0.0537] levels at week 8 following initiation of infliximab + GMA therapy. Nine patients who received combination therapy achieved remission, which was maintained to week 24 with infliximab alone. Additionally, cutaneous lesions in two patients with IR were improved. ATI-CAI assay efficiency was not influenced by infliximab concentration during the test. Pre- and post-infliximab infusion ATI levels were not different. Patients with ATI greater than the 0.153 μg/mL cut-off value were likely to experience LOR [odds ratio 3.0].
Patients who received infliximab + GMA therapy appeared to regain clinical response to infliximab by a decrease in ATI level. Furthermore, the concentration of infliximab in the test did not influence ATI measurement, but was associated with clinical response.
在炎症性肠病(IBD)患者中,针对英夫利昔单抗(ATI)的产生与英夫利昔单抗的失应答(LOR)和输注反应(IR)有关。免疫治疗方法被认为是克服 LOR 的一种选择。已有研究表明,使用 Adacolumn 进行粒细胞/单核细胞吸附性血浆分离术(GMA)可在 IBD 患者中产生临床疗效,并具有免疫调节作用。
我们开发了一种利用固定化 C1q 的板的 ATI-CAI 检测方法,并将其应用于接受英夫利昔单抗治疗的患者,包括 56 例持续应答者、76 例 LOR 患者和 6 例 IR 患者。此外,分析了 14 例 LOR 患者和 2 例出现反常皮肤反应的患者,他们接受了英夫利昔单抗+GMA 联合治疗。
14 例 LOR 患者(7 例克罗恩病,7 例溃疡性结肠炎)在开始英夫利昔单抗+GMA 治疗后的第 8 周,临床指标显著改善(p=0.0009),ATI(p=0.0171)和白细胞介素-6(p=0.0537)水平降低。9 例接受联合治疗的患者达到缓解,在单独使用英夫利昔单抗的第 24 周仍保持缓解。此外,2 例 IR 患者的皮肤病变得到改善。ATI-CAI 检测效率不受检测过程中英夫利昔单抗浓度的影响。在英夫利昔单抗输注前后,ATI 水平无差异。ATI 大于 0.153μg/mL 截断值的患者更有可能出现 LOR[比值比 3.0]。
接受英夫利昔单抗+GMA 治疗的患者似乎通过降低 ATI 水平恢复了对英夫利昔单抗的临床应答。此外,检测中的英夫利昔单抗浓度不影响 ATI 测定,但与临床反应相关。