Takagi Tomohisa, Uchiyama Kazuhiko, Asaeda Kohei, Murakami Eiki, Inoue Ken, Mizushima Katsura, Hirai Yasuko, Naito Yuji, Itoh Yoshito
Molecular Gastroenterology and Hepatology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Department for Medical Innovation and Translational Medical Science, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
J Gastroenterol Hepatol. 2025 Jul;40(7):1719-1727. doi: 10.1111/jgh.17000. Epub 2025 May 24.
The association between vascular cell adhesion molecule-1 (VCAM-1) expression and intestinal mucosal inflammation and between VCAM-1 expression and the clinical course in patients with ulcerative colitis (UC) remains unclear. Therefore, we investigated not only the association between mucosal VCAM-1 expression and mucosal inflammation but also its association with subsequent relapse in UC patients with clinical remission.
Fifty-eight patients with UC in clinical remission and 16 patients in clinical active who visited Kyoto Prefectural University of Medicine for a 2-year follow-up period were included. VCAM-1 expression was compared between patients who subsequently relapsed and those who remained in remission, and it was examined in relation to endoscopic findings, histological activity, and cytokine expression. We also investigated the expression of mucosal addressin cell adhesion molecule-1 (MAdCAM-1).
VCAM-1 was associated with clinical disease activity and endoscopic severity and was significantly elevated in histologically active mucosa compared with inactive mucosa. VCAM-1 expression co-localized with MAdCAM-1 in the mucosal and submucosal microvessels of the colon and was significantly higher in the relapse group than in the remission group. Similar results were observed for MAdCAM-1 expression. VCAM-1 expression levels were also closely correlated with those of several other cytokines.
VCAM-1 expression in the colonic mucosa of patients with UC is associated with mucosal inflammation and subsequent relapse. These results suggest that VCAM-1 may serve as a marker for relapse and therapeutic effectiveness in UC, and that treatment targeting α4 integrin is efficient and rational.
血管细胞黏附分子-1(VCAM-1)表达与肠道黏膜炎症之间的关联,以及VCAM-1表达与溃疡性结肠炎(UC)患者临床病程之间的关联仍不明确。因此,我们不仅研究了黏膜VCAM-1表达与黏膜炎症之间的关联,还研究了其与临床缓解的UC患者随后复发之间的关联。
纳入了58例临床缓解期的UC患者和16例临床活动期患者,这些患者在京都府立医科大学接受了为期2年的随访。比较了随后复发的患者和仍处于缓解期的患者之间的VCAM-1表达,并研究了其与内镜检查结果、组织学活性和细胞因子表达的关系。我们还研究了黏膜地址素细胞黏附分子-1(MAdCAM-1)的表达。
VCAM-1与临床疾病活动度和内镜严重程度相关,与非活动黏膜相比,组织学活性黏膜中的VCAM-1显著升高。VCAM-1表达与MAdCAM-1在结肠黏膜和黏膜下微血管中共定位,复发组中的表达明显高于缓解组。MAdCAM-1表达也观察到类似结果。VCAM-1表达水平还与其他几种细胞因子的表达密切相关。
UC患者结肠黏膜中的VCAM-1表达与黏膜炎症及随后的复发相关。这些结果表明,VCAM-1可能作为UC复发和治疗效果的标志物,并且靶向α4整合素的治疗是有效且合理的。