Treatment-refractory ulcerative colitis responsive to indigo naturalis.


Journal

BMJ open gastroenterology
ISSN: 2054-4774
Titre abrégé: BMJ Open Gastroenterol
Pays: England
ID NLM: 101660690

Informations de publication

Date de publication:
12 2021
Historique:
received: 10 11 2021
accepted: 10 12 2021
entrez: 31 12 2021
pubmed: 1 1 2022
medline: 26 4 2022
Statut: ppublish

Résumé

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.

Sections du résumé

BACKGROUND
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.
METHODS
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.
RESULTS
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.
CONCLUSION
IN is a potentially effective therapy for patients with treatment-refractory ulcerative colitis. This benefit is likely through AhR activation.
TRIAL REGISTRATION NUMBER
NCT02442960.

Identifiants

pubmed: 34969665
pii: bmjgast-2021-000813
doi: 10.1136/bmjgast-2021-000813
pmc: PMC8718466
pii:
doi:

Substances chimiques

RNA 63231-63-0
Indigo Carmine D3741U8K7L
Cytochrome P-450 CYP1A1 EC 1.14.14.1

Banques de données

ClinicalTrials.gov
['NCT02442960']

Types de publication

Clinical Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: JPS and MGD are employed by and have equity in Azora Therapeutics and are co-inventors on a patent for compositions comprising indigo and/or an indigo derivative. JOLA has equity in Azora Therapeutics and is a co-inventor on a patent for compositions comprising indigo and/or an indigo derivative. LRF has stock in Azora Therapeutics related to advisory activities. BL is currently employed at the University of California, Los Angeles and has stock in Azora Therapeutics related to advisory activities. KTP declares no competing interest during the study, is an employee of Genentech, and shareholder of the Roche Group.

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Auteurs

Julie P Saiki (JP)

Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, California, USA.

Johan Ol Andreasson (JO)

Department of Genetics, Department of Biochemistry, Stanford University School of Medicine, Stanford, California, USA.

Kevin V Grimes (KV)

Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, California, USA.

Lyn R Frumkin (LR)

Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, California, USA.

Elvi Sanjines (E)

Division of Gastroenterology and Hepatology, Stanford University School of Medicine, Stanford, California, USA.

Matthew G Davidson (MG)

Azora Therapeutics Inc, Encino, California, USA.

K T Park (KT)

Division of Pediatric Gastroenterology, Stanford University School of Medicine, Stanford, California, USA.

Berkeley Limketkai (B)

Division of Gastroenterology and Hepatology, Stanford University School of Medicine, Stanford, California, USA blimketkai@mednet.ucla.edu.

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Classifications MeSH