The Role of Sodium Chloride and the Treg/Th17 Axis in Autoimmune Hepatitis

Not Applicable

Completed

• Conditions: Autoimmune Hepatitis
• Interventions: Other: Low Salt Diet; Other: Liberal salt diet

• Registration Number: NCT02050646
• Lead Sponsor: Yale University

Brief Summary

The purpose of this study is to determine whether a salt restriction diet improves immune parameters in patients with autoimmune hepatitis.

Detailed Description

The etiology of autoimmune hepatitis (AIH) is unknown although both genetic and environmental factors are thought to be involved. A defect in immune regulation affecting regulatory T cells (Tregs) has been demonstrated in AIH. Tregs function in the maintenance of immune homeostasis by controlling autoreactive immune responses to self-antigens.

Rationale: the western diet has been postulated as a potential environmental risk factor for the increasing incidence of autoimmune diseases in developed countries. Data from the investigators' laboratory also suggests that increased dietary salt intake might represent an environmental risk factor for the development of autoimmune diseases through the induction of pathogenic Th17 cells. The dramatic in vitro effects of high salt on the induction of pathogenic Th17 cells from naïve human CD4 cells {Kleinewietfeld, Hafler. Nature. 2013 Apr 25;496(7446):518-22. doi: 10.1038/nature11868.}, and block of in vitro Treg suppression, in line with in vivo effects on worsening murine experimental autoimmune encephalomyelitis (EAE), have prompted the investigators to examine the effects of increased dietary sodium chloride in a human in vivo system.

The investigators hypothesize that excess dietary salt may function as an environmental trigger that favors induction and expansion of pathogenic Th17 cells and leads to functional impairment of Tregs, thereby favoring development of autoimmunity. The investigators aim to study their established in vitro model in humans by altering the salt intake in patients over a 20-day period.

Study Timeline

• Study Start: 2013-08-27
• Study First Submitted: 2013-11-04
• Study First Submitted QC: 2014-01-28
• Study First Posted: 2014-01-31
• Primary Completion: 2019-08
• Study Completion: 2021-06
• Status Verified: 2021-07
• Last Update Submitted: 2021-07-27
• Last Update Posted: 2021-07-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 16

Inclusion Criteria

• Adults 18-50 years of age
• Children 1-17 years of age
• ALT and/or ALP/GGT level > 2X upper limit of normal
• ANA or SMA >/= 1:40
• ANA or SMA >/= 1:80
• or LKM >/= 1:40
• or SLA positive
• IgG > upper limit of normal

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Exclusion Criteria

• Chronic hepatitis C
• Decompensated Liver Disease

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Liberal salt/Low salt diet	Low Salt Diet	Cross-over trial of low salt and liberal salt diet
Liberal salt/Low salt diet	Liberal salt diet	Cross-over trial of low salt and liberal salt diet
Low salt/ Liberal salt Diet	Low Salt Diet	Cross-over trial of liberal salt and low salt diet.
Low salt/ Liberal salt Diet	Liberal salt diet	Cross-over trial of liberal salt and low salt diet.

Primary Outcome Measures

Name	Time	Method
Change from baseline in production of pathogenic TH17 cells.	26 days	Measuring TH17 cells by flow cytometry and qRT-PCR. There are no known normal ranges. The investigator will calculate the change by observing the difference from baseline values.

Secondary Outcome Measures

Name	Time	Method
Change from baseline in regulatory T cell function.	26 days	Measuring T cell function by flow cytometry. There are no known normal ranges. The investigator will calculate the change by observing the difference from baseline values.