Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, California, USA.
Department of Genetics, Department of Biochemistry, Stanford University School of Medicine, Stanford, California, USA.
BMJ Open Gastroenterol. 2021 Dec;8(1). doi: 10.1136/bmjgast-2021-000813.
Indigo naturalis (IN) is an herbal medicine that has been used for ulcerative colitis with an unclear mechanism of action. Indigo and indirubin, its main constituents, are ligands of the aryl hydrocarbon receptor (AhR). We assessed the safety, efficacy, and colon AhR activity of IN given orally to patients with treatment-refractory ulcerative colitis. The role of AhR in IN benefit was further evaluated with an AhR antagonist in a murine colitis model.
This open-label, dose-escalation study sequentially treated 11 patients with ulcerative colitis with either IN 500 mg/day or 1.5 g/day for 8 weeks, followed by a 4-week non-treatment period. The primary efficacy endpoint was clinical response at week 8, assessed by total Mayo score. Secondary endpoints included clinical remission, Ulcerative Colitis Endoscopic Index of Severity, quality of life, and colon AhR activity measured by cytochrome P450 1A1 (CYP1A1) RNA expression.
Ten of 11 (91%) patients, including 8/9 (89%) with moderate-to-severe disease, achieved a clinical response. Among these 10 patients, all had failed treatment with 5-aminosalicylic acid, 8 patients with a tumour necrosis factor (TNF)-alpha inhibitor, and 6 patients with TNF-alpha inhibitor and vedolizumab. Five patients were corticosteroid dependent. Clinical response was observed in all five patients who had been recommended for colectomy. Three patients achieved clinical remission. All patients experienced improved endoscopic severity and quality of life. Four weeks after treatment completion, six patients had worsened partial Mayo scores. Four patients progressed to colectomy after study completion. Colon CYP1A1 RNA expression increased 12 557-fold at week 8 among six patients evaluated. No patient discontinued IN due to an adverse event. Concomitant administration of 3-methoxy-4-nitroflavone, an AhR antagonist, in a murine colitis model abrogated the benefit of IN.
IN is a potentially effective therapy for patients with treatment-refractory ulcerative colitis. This benefit is likely through AhR activation.
NCT02442960.
靛蓝天然物(IN)是一种草药,已被用于溃疡性结肠炎,但其作用机制尚不清楚。靛蓝和其主要成分靛玉红是芳烃受体(AhR)的配体。我们评估了口服 IN 治疗难治性溃疡性结肠炎患者的安全性、疗效和结肠 AhR 活性。在小鼠结肠炎模型中,我们用 AhR 拮抗剂进一步评估了 AhR 在 IN 获益中的作用。
这项开放标签、剂量递增的研究连续对 11 例溃疡性结肠炎患者进行 IN 治疗,剂量分别为 500mg/天或 1.5g/天,治疗 8 周,然后进行 4 周非治疗期。主要疗效终点是第 8 周的总 Mayo 评分评估的临床缓解。次要终点包括临床缓解、溃疡性结肠炎内镜指数严重程度、生活质量和通过细胞色素 P450 1A1(CYP1A1)RNA 表达测量的结肠 AhR 活性。
11 例患者中的 10 例(91%),包括 9 例中重度疾病患者中的 8 例(89%)达到了临床缓解。在这 10 例患者中,所有患者均对 5-氨基水杨酸治疗失败,8 例对 TNF-α抑制剂治疗失败,6 例对 TNF-α抑制剂和 vedolizumab 治疗失败。5 例患者依赖皮质类固醇。所有推荐行结肠切除术的患者均观察到临床缓解。3 例患者达到临床缓解。所有患者的内镜严重程度和生活质量均得到改善。治疗结束后 4 周,6 例患者的部分 Mayo 评分恶化。研究结束后,4 例患者进展为结肠切除术。在 6 例接受评估的患者中,第 8 周结肠 CYP1A1 RNA 表达增加了 12557 倍。没有患者因不良反应而停止 IN 治疗。在小鼠结肠炎模型中,同时给予 AhR 拮抗剂 3-甲氧基-4-硝基黄酮可消除 IN 的获益。
IN 可能是一种治疗难治性溃疡性结肠炎患者的有效治疗方法。这种益处可能是通过 AhR 激活实现的。
NCT02442960。