英夫利昔单抗与肠黏膜肿瘤坏死因子α测定:临床新工具?

S. Pecere, V. Petito, A. Amato, A. Poscia, A. Armuzzi, L. Lopetuso, A. Sgambato, G. Cammarota, A. Papa, A. Gasbarrini, F. Scaldaferri
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引用次数: 3

摘要

背景:英夫利昔单抗(IFX)谷水平测量可以部分解释对该药物反应的损失机制。然而,关于其在粘膜水平的浓度或粘膜药代动力学的信息很少。目的:本研究的目的是探讨IFX是否可以在肠粘膜内测量,以及是否可以假设粘膜水平、血清水平和临床反应之间的相关性。方法:纳入了15例连续接受稳定剂量IFX的炎症性肠病患者,并行内窥镜检查。从受感染和未受影响的区域进行活检,培养48小时,并收集血清样本。使用市售的酶联免疫吸附测定试剂盒检测IFX和肿瘤坏死因子α (TNF-α)水平。结果:在80%的结肠活检上清液和60%的血清样本中检测到IFX水平。100%的患者可检测到TNF-α肠黏膜水平,75%的患者可检测到TNF-α血清水平。粘膜和血清中IFX和TNF-α水平无相关性;最后一次输注与血清或肠黏膜水平无相关性。在对IFX治疗无反应的患者的粘膜中,IFX的水平更常检测不到。结论:肠黏膜可检测到IFX和TNF-α水平。IFX粘膜水平可用于将患者分为对IXF治疗有反应和无反应的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Infliximab and Tumour Necrosis Factor Alpha Measurement on Intestinal Mucosa: A New Tool for the Clinic?
Background: Infliximab (IFX) trough levels measurement could partially explain mechanisms of loss in response to this drug. However, little information exists on its concentration at the mucosal level or mucosal pharmacokinetics. Objective: The aim of this study was to investigate whether IFX could be measured within intestinal mucosa, and whether a correlation between mucosal level, serum level, and clinical response could be hypothesised. Methods: Fifteen consecutive patients with inflammatory bowel disease receiving stable doses of IFX who underwent endoscopy were enrolled. Biopsies were taken from an affected and an unaffected area and cultured for 48 hours, and serum samples were also collected. IFX and tumour necrosis factor alpha (TNF-α) levels were measured using commercially available enzyme-linked immunosorbent assay kits. Results: IFX levels were detected in 80% of the colonic biopsy supernatants and in 60% of the serum samples. TNF-α intestinal mucosal levels were detectable in 100% of patients, while TNF-α serum levels were detectable in 75%. Mucosal and serum levels of IFX and TNF-α did not correlate; no correlation was found between the last infusion and serum or intestinal mucosal levels. Levels of IFX were more frequently undetectable in the mucosa of patients not responding to IFX therapy. Conclusions: Detectable levels of IFX and TNF-α can be found in intestinal mucosa. IFX mucosa levels could be useful to stratify patients into responders and non-responders to IXF therapy.
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