Department of Biochemistry, P. D. Hinduja Hospital, Veer Savarkar Marg, Mahim, Mumbai, 400 016, India.
Division of Gastroenterology, P. D. Hinduja Hospital, Veer Savarkar Marg, Mahim, Mumbai, 400 016, India.
Indian J Gastroenterol. 2020 Oct;39(5):426-434. doi: 10.1007/s12664-020-01050-x. Epub 2020 Oct 29.
Infliximab (IFX) monitoring has been proposed for effective therapeutic management of inflammatory bowel disease (IBD). There is no data on infliximab levels and its antibody measurement in Indian patients. We assessed the clinical efficacy of IFX level and antibodies to infliximab (ATI) monitoring in IBD patients.
Infliximab trough level and antibody testing was done in 50 and 30 IBD patients, respectively using commercially available enzyme-linked immunosorbent assay (ELISA) kits. The levels were correlated with the disease status, albumin, and C-reactive protein (CRP) levels. The clinical efficacy of level-based change in patient management was evaluated.
Of 50 patients, IFX levels were therapeutic in 8, sub-therapeutic in 40, and supra-therapeutic in 2. High ATI titer was present in 8/30 patients. The IFX level did not correlate with the dose of 5 or 10 mg/kg. Based on IFX level and ATI estimation, management was changed in 35 patients: increase in dose in 7, decrease in dosing interval in 17, increase in interval in 2, surgery in 2, change in biologic in 5, and cessation of IFX in 2 patients. Therapy modification based on IFX level improved the clinical response in 25 patients, of whom 5 are in remission at a median duration of 2 years.
Most (80%) of the IBD patients had subtherapeutic IFX levels while high ATI titers were found in 27% of the patients. There was no correlation between infliximab dose and drug levels. Therapy modification based on drug level benefitted the majority. Our results suggest that measurement of IFX level assists in attaining therapeutic levels and improves clinical response.
英夫利昔单抗(IFX)监测被提议用于炎症性肠病(IBD)的有效治疗管理。目前尚无印度患者英夫利昔单抗水平及其抗体检测的数据。我们评估了 IBD 患者中 IFX 水平和抗英夫利昔单抗抗体(ATI)监测的临床疗效。
使用市售酶联免疫吸附试验(ELISA)试剂盒分别对 50 例和 30 例 IBD 患者进行英夫利昔单抗谷值水平和抗体检测。将水平与疾病状态、白蛋白和 C 反应蛋白(CRP)水平相关联。评估基于患者管理的水平变化的临床疗效。
50 例患者中,8 例 IFX 水平为治疗性,40 例为亚治疗性,2 例为超治疗性。30 例患者中有 8 例存在高 ATI 滴度。IFX 水平与 5 或 10mg/kg 的剂量无关。根据 IFX 水平和 ATI 估计,对 35 例患者进行了治疗管理的改变:增加剂量 7 例,减少给药间隔 17 例,增加间隔 2 例,手术 2 例,改变生物制剂 5 例,2 例停止使用 IFX。基于 IFX 水平的治疗方法改变改善了 25 例患者的临床反应,其中 5 例在中位 2 年时处于缓解状态。
大多数(80%)IBD 患者的 IFX 水平为亚治疗性,而 27%的患者存在高 ATI 滴度。英夫利昔单抗剂量与药物水平之间无相关性。基于药物水平的治疗方法改变使大多数患者受益。我们的结果表明,IFX 水平的测量有助于达到治疗水平并改善临床反应。