Merras-Salmio Laura, Kolho Kaija-Leena
Department of Pediatric Gastroenterology, Helsinki University Hospital, Children's Hospital and University of Helsinki, Helsinki, Finland.
J Pediatr Gastroenterol Nutr. 2017 Feb;64(2):272-278. doi: 10.1097/MPG.0000000000001258.
Optimizing infliximab (IFX) treatment in pediatric patients with inflammatory bowel disease (IBD) by using serum infliximab (S-IFX) trough levels and antibodies to IFX is recommended. There is need for studies assessing this strategy in clinical practice.
We retrospectively identified all pediatric patients with IBD (n = 146, median age 14.8 years) treated with IFX at our tertiary referral center from 2003 to 2014. All were analyzed for IFX trough levels (S-IFX, n = 475), and IFX antibody (IFX-Ab, n = 219) titers were included. Both were analyzed using enzyme-linked immunosorbent assay. We correlated these parameters with concurrently analyzed fecal calprotectin levels and the treatment outcome.
If IFX had no efficacy, or a loss of response occurred, 40 of 64 (63%) had trough levels <2.0 mg/L, with negative IFX-Ab in 37 of 59 (63%). If the S-IFX was very low (<0.2 mg/L), 4 of 36 still had negative IFX-Ab. Concurrent azathioprine therapy did not relate to IFX-Ab. Fecal calprotectin was significantly lower in patients with clinical remission or ongoing therapy compared with those with subsequent loss of efficacy: medians 95 μg/g (33-308) and 670 μg/g (264-1473), P < 0.0001. The S-IFX median was substantially higher in patients with either remission or ongoing therapy, compared with those with no or loss of efficacy: 3.7 mg/L (1.8-5.4) and 1.2 mg/L (0.03-4.4, P = 0.01), respectively.
Measuring IFX trough levels and fecal calprotectin has a potential impact on the treatment strategies and should be included in clinical routine. Low IFX trough levels associate with increased antibodies to IFX in most, but not in all cases.
推荐通过监测血清英夫利昔单抗(S-IFX)谷浓度和抗英夫利昔单抗抗体来优化炎症性肠病(IBD)患儿的英夫利昔单抗(IFX)治疗。需要在临床实践中评估该策略的研究。
我们回顾性纳入了2003年至2014年在我们三级转诊中心接受IFX治疗的所有IBD患儿(n = 146,中位年龄14.8岁)。对所有患儿进行了IFX谷浓度(S-IFX,n = 475)分析,并检测了英夫利昔单抗抗体(IFX-Ab,n = 219)滴度。两者均采用酶联免疫吸附测定法进行分析。我们将这些参数与同时分析的粪便钙卫蛋白水平及治疗结果进行了关联分析。
若IFX无效或出现疗效丧失,64例中有40例(63%)谷浓度<2.0 mg/L,59例中有37例(63%)IFX-Ab阴性。若S-IFX极低(<0.2 mg/L),36例中有4例IFX-Ab仍为阴性。同时使用硫唑嘌呤治疗与IFX-Ab无关。与后续出现疗效丧失的患者相比,临床缓解或持续治疗的患者粪便钙卫蛋白显著降低:中位数分别为95 μg/g(33 - 308)和670 μg/g(264 - 1473),P < 0.0001。与无疗效或疗效丧失的患者相比,缓解或持续治疗的患者S-IFX中位数显著更高:分别为3.7 mg/L(1.8 - 5.4)和1.2 mg/L(0.03 - 4.4,P = 0.01)。
检测IFX谷浓度和粪便钙卫蛋白可能会对治疗策略产生影响,应纳入临床常规检查。大多数但并非所有情况下,低IFX谷浓度与抗IFX抗体增加相关。