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一项 1 期开放标签试验表明,Smad7 反义寡核苷酸(GED0301)不会增加克罗恩病患者小肠狭窄的风险。

A phase 1 open-label trial shows that smad7 antisense oligonucleotide (GED0301) does not increase the risk of small bowel strictures in Crohn’s disease.

机构信息

Department of Systems Medicine, University of Rome ‘Tor Vergata’, Rome, Italy.

出版信息

Aliment Pharmacol Ther. 2012 Nov;36(9):850-7. doi: 10.1111/apt.12051.

Abstract

BACKGROUND

In Crohn's disease (CD), knockdown of Smad7, an inhibitor of Transforming Growth Factor (TGF)-β1 activity, with a specific antisense oligonucleotide (GED0301) seems to be safe and tolerable and associates with TGF-β1-mediated suppression of inflammatory pathways.

AIM

Since TGF-β1 has pro-fibrogenic effects in many organs, we evaluated whether GED0301 treatment associates with the formation of small bowel strictures.

METHODS

Fifteen patients with active, inflammatory CD, receiving oral GED0301 once daily for 7 days, were monitored for the formation of small bowel strictures by Small Intestine Contrast Ultrasonography (SICUS). Serum basic fibroblast growth factor (bFGF) and human chitinase 3-like 1 (also known as YKL-40), two markers of CD-related intestinal strictures, and matrix metalloproteinases (MMP) and tissue inhibitor 1 of MMPs (TIMP1) were analysed at day 0 and day 180 by ELISA. Crohn's disease activity index (CDAI) changes were also monitored.

RESULTS

Fourteen patients completed the 6-month study; the remaining underwent intestinal resection for a severe relapse not responsive to medical treatment. No patient developed small bowel stricture and none experienced obstructive symptoms during the study period. GED0301 treatment induced no significant change in the circulating levels of bFGF, YKL-40, MMPs and TIMP1. Seven of 12 patients who reached clinical remission following GED0301 treatment maintained a CDAI < 150 at day 180.

CONCLUSION

Short-term treatment of patients with Crohn's disease using GED0301 is not associated with the development of small bowel stricture, thus reinforcing the concept that this drug is safe at least at early time points.

摘要

背景

在克罗恩病(CD)中,用特定的反义寡核苷酸(GED0301)敲低转化生长因子(TGF)-β1 活性的抑制剂 Smad7 似乎是安全且耐受的,并与 TGF-β1 介导的炎症途径抑制有关。

目的

由于 TGF-β1 在许多器官中具有促纤维化作用,我们评估了 GED0301 治疗是否与小肠狭窄的形成有关。

方法

15 例活动性炎症性 CD 患者每天口服 GED0301 一次,共 7 天,通过小肠对比超声(SICUS)监测小肠狭窄的形成。在第 0 天和第 180 天,通过 ELISA 分析血清碱性成纤维细胞生长因子(bFGF)和人几丁质酶 3 样 1(也称为 YKL-40),这两种 CD 相关肠道狭窄标志物,以及基质金属蛋白酶(MMPs)和基质金属蛋白酶抑制剂 1(TIMP1)。同时监测克罗恩病活动指数(CDAI)的变化。

结果

14 例患者完成了 6 个月的研究;其余患者因对药物治疗无反应的严重复发而接受了肠切除术。在研究期间,没有患者出现小肠狭窄,也没有出现阻塞症状。GED0301 治疗没有引起循环 bFGF、YKL-40、MMPs 和 TIMP1 水平的显著变化。在接受 GED0301 治疗后达到临床缓解的 12 例患者中有 7 例在第 180 天 CDAI<150。

结论

在克罗恩病患者中使用 GED0301 进行短期治疗与小肠狭窄的发展无关,这进一步证实了该药物在早期至少是安全的。

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