Pauwels Renske W M, Proietti Elisa, van der Woude Christien J, Oudijk Lindsey, Crombag Marie-Rose B S, Peppelenbosch Maikel P, Grohmann Ursula, Fuhler Gwenny M, de Vries Annemarie C
Erasmus MC, Department of Gastroenterology and Hepatology, Rotterdam, the Netherlands.
University of Perugia, Department of Experimental Medicine, Perugia, Italy.
Inflamm Bowel Dis. 2021 Oct 20;27(11):1813-1820. doi: 10.1093/ibd/izab053.
The association between vedolizumab (VDZ) exposure and treatment response is unclear and seems insufficiently explained by serum levels. The aim of this study was to assess the correlation between VDZ concentrations in serum and intestinal tissue and their association with mucosal inflammation and response to VDZ.
This prospective study included 37 adult patients with inflammatory bowel disease with endoscopic inflammation at baseline who started VDZ. At week 16, serum and biopsies were collected for VDZ measurement by enzyme-linked immunosorbent assay. Nonlinear mixed-effects modeling was used to calculate serum trough concentrations and to assess intestinal tissue concentrations. Validated clinical and endoscopic scores were used to define clinical and endoscopic response and remission, and fecal calprotectin levels were used to assess biochemical response. Histologic remission was determined by the Nancy score.
A positive correlation was observed between VDZ concentrations in serum and tissue (r2 = 0.83; P < 0.0001). High mucosal rather than serum VDZ levels correlated with a reduced endoscopic (P = 0.06) grade of mucosal inflammation. Furthermore, patients with a positive biochemical and endoscopic outcome had higher tissue levels of VDZ than patients without biochemical and endoscopic response (P < 0.01 and P = 0.04, respectively).
Tissue levels of VDZ may provide a better marker than serum levels for mucosal inflammation and objective treatment outcome at week 16. The potential of VDZ tissue levels for therapeutic drug monitoring in inflammatory bowel disease warrants further exploration.
维多珠单抗(VDZ)暴露与治疗反应之间的关联尚不清楚,血清水平似乎也无法充分解释这种关联。本研究的目的是评估血清和肠道组织中VDZ浓度之间的相关性,以及它们与黏膜炎症和对VDZ反应的关联。
这项前瞻性研究纳入了37例基线时患有炎症性肠病且有内镜下炎症的成年患者,这些患者开始使用VDZ治疗。在第16周时,采集血清和活检样本,通过酶联免疫吸附测定法测量VDZ。使用非线性混合效应模型计算血清谷浓度并评估肠道组织浓度。使用经过验证的临床和内镜评分来定义临床和内镜反应及缓解情况,并使用粪便钙卫蛋白水平评估生化反应。通过南希评分确定组织学缓解情况。
观察到血清和组织中VDZ浓度之间呈正相关(r2 = 0.83;P < 0.0001)。高黏膜VDZ水平而非血清VDZ水平与黏膜炎症内镜分级降低相关(P = 0.06)。此外,生化和内镜结果为阳性的患者的组织VDZ水平高于无生化和内镜反应的患者(分别为P < 0.01和P = 0.04)。
在第16周时,VDZ的组织水平可能比血清水平更能作为黏膜炎症和客观治疗结果的更好标志物。VDZ组织水平在炎症性肠病治疗药物监测中的潜力值得进一步探索。