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儿科克罗恩病的血清免疫分析表明,与传统治疗相比,一线使用英夫利昔单抗具有更强的免疫调节作用,且治疗前的特征可预测两种治疗方法的临床应答。

Serum Immune Profiling in Paediatric Crohn's Disease Demonstrates Stronger Immune Modulation With First-Line Infliximab Than Conventional Therapy and Pre-Treatment Profiles Predict Clinical Response to Both Treatments.

机构信息

Department of Pediatric Gastroenterology, Erasmus University Medical Center/Sophia Children's Hospital, Rotterdam, the Netherlands.

Laboratory of Pediatrics, Division of Gastroenterology and Nutrition, Erasmus University Medical Center/Sophia Children's Hospital, Rotterdam, the Netherlands.

出版信息

J Crohns Colitis. 2023 Aug 21;17(8):1262-1277. doi: 10.1093/ecco-jcc/jjad049.

Abstract

BACKGROUND

Despite its efficacy, rational guidance for starting/stopping first-line biologic treatment in individual paediatric Crohn's disease [CD] patients is needed. We assessed how serum immune profiles before and after first-line infliximab [FL-IFX] or conventional [CONV] induction therapy associate with disease remission at week 52.

METHODS

Pre- [n = 86], and 10-14-week post-treatment [n = 84] sera were collected from patients with moderate-to-severe paediatric CD in the TISKids trial, randomized to FL-IFX [n = 48; five 5-mg/kg infusions over 22 weeks] or CONV [n = 43; exclusive enteral nutrition or oral prednisolone]; both groups received azathioprine maintenance. The relative concentrations of 92 inflammatory proteins were determined with Olink Proteomics; fold changes [FC] with |log2FC| > 0.5 after false discovery rate adjustment were considered significant.

RESULTS

FL-IFX modulated a larger number of inflammatory proteins and induced stronger suppression than CONV; 18/30 proteins modulated by FL-IFX were not regulated by CONV. Hierarchical clustering based on IFX-modulated proteins at baseline revealed two clusters of patients: CD-hi patients had significantly higher concentrations of 23/30 IFX-modulated proteins [including oncostatin-M, TNFSF14, HGF and TGF-α], and higher clinical disease activity, C-reactive protein and blood neutrophils at baseline than CD-lo patients. Only 24% of CD-hi FL-IFX-treated patients maintained remission without escalation at week 52 vs 58% of CD-lo FL-IFX-treated patients. Similarly, 6% of CD-hi CONV-treated patients achieved remission vs 20% of CONV-treated CD-lo patients. Clustering based on immune profiles post-induction therapy did not relate to remission at week 52.

CONCLUSION

FL-IFX leads to stronger reductions and modulates more immune proteins than CONV. Stratification on pre-treatment profiles of IFX-modulated proteins directly relates to maintenance of remission without treatment escalation.

TRIAL REGISTRATION NUMBER

NCT02517684.

摘要

背景

尽管疗效显著,但仍需要为个体儿童克罗恩病患者提供关于一线生物制剂治疗起始/停止的合理指导。我们评估了一线英夫利昔单抗(FL-IFX)或常规(CONV)诱导治疗前后的血清免疫谱与第 52 周时疾病缓解的关系。

方法

在 TISKids 试验中,我们从患有中重度儿童 CD 的患者中采集了治疗前(n=86)和治疗后 10-14 周(n=84)的血清,这些患者被随机分配到 FL-IFX(n=48;5 次 5mg/kg 输注,持续 22 周)或 CONV 组(n=43;单纯肠内营养或口服泼尼松龙);两组均接受硫唑嘌呤维持治疗。使用 Olink 蛋白质组学测定 92 种炎症蛋白的相对浓度;经错误发现率调整后,|log2FC|>0.5 的倍数变化(FC)被认为具有统计学意义。

结果

FL-IFX 调节的炎症蛋白数量多于 CONV,抑制作用更强;FL-IFX 调节的 18/30 种蛋白不受 CONV 调节。基于基线时 IFX 调节蛋白的层次聚类显示了两类患者:CD-hi 患者的 23/30 种 IFX 调节蛋白浓度显著更高[包括肿瘤坏死因子-α、肿瘤坏死因子配体超家族成员 14、肝细胞生长因子和转化生长因子-α],且基线时临床疾病活动度、C 反应蛋白和血液中性粒细胞更高,而 CD-lo 患者则更低。在第 52 周时,只有 24%的 CD-hi 接受 FL-IFX 治疗的患者无需升级治疗即可维持缓解,而 58%的 CD-lo 接受 FL-IFX 治疗的患者则可维持缓解。同样,6%的 CD-hi 接受 CONV 治疗的患者达到缓解,而接受 CONV 治疗的 CD-lo 患者中则有 20%达到缓解。基于诱导治疗后免疫谱的聚类与第 52 周时的缓解无关。

结论

FL-IFX 导致的降低幅度和调节的免疫蛋白比 CONV 更多。基于 IFX 调节蛋白的治疗前谱的分层与无需升级治疗即可维持缓解直接相关。

试验注册号

NCT02517684。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c766/10441564/74feba7c062b/jjad049_fig8.jpg

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