A Role for RAGE/TXNIP/Inflammasome Axis in Alveolar Macrophage Activation During ARDS (RIAMA): a Proof-of-concept Clinical Study

Completed

• Conditions: Mechanical Ventilation; Acute Respiratory Distress Syndrome
• Interventions: Other: RAGE TXNIP Inflammasome axis

• Registration Number: NCT02545621
• Lead Sponsor: University Hospital, Clermont-Ferrand

Brief Summary

RAGE (the receptor for advanced glycation end-products) is a marker of alveolar type I cell injury and a pivotal mediator of acute inflammation and innate immunity. RAGE pathway is highly regulated; the interaction of the transmembrane receptor with its various ligands (e.g. HMGB1, S100A12) ultimately leads to NF-kB activation and RAGE upregulation itself, but precise RAGE functions and intracellular pathways remain underexplored. During ARDS, monocyte and macrophage activation could modulate alveolar inflammation and repair.

As RAGE is also expressed at the surface of monocytes/macrophages, we hypothesize that alveolar monocyte/macrophage activation may be mediated through a RAGE-TXNIP (thioredoxin interacting protein)-NLRP3/inflammasome intracellular pathway. The purpose of this observational prospective study is to compare alveolar monocyte/macrophage activation profiles (as assessed by Fluorescence-Activated Cell Sorting (FACS)) in mechanically ventilated patients with or without ARDS.

Detailed Description

BACKGROUND:

The receptor for advanced glycation end products (RAGE) was recently identified as a promising new marker of alveolar type I cell injury. RAGE is a member of the immunoglobulin superfamily that acts as a multiligand receptor and is involved in propagating inflammatory responses in various cell populations. While the precise function of RAGE remains unclear, the elevated levels of RAGE, and its soluble isoform sRAGE, correlate with severity of acute respiratory distress syndrome (ARDS) in human and animal studies.

RAGE pathway is highly regulated; the interaction of the transmembrane receptor with its various ligands (e.g. HMGB1, S100A12) ultimately leads to NF-kB activation and RAGE upregulation itself. During ARDS, monocyte and macrophage activation could modulate alveolar inflammation and repair. As RAGE is also expressed at the surface of monocytes/macrophages, we hypothesize that alveolar monocyte/macrophage activation may be mediated through a RAGE-TXNIP (thioredoxin interacting protein)-NLRP3/inflammasome intracellular pathway.

DESIGN NARRATIVE:

The purpose of this monocentric observational prospective pathophysiology study is to compare alveolar monocyte/macrophage activation profiles between patients with or without ARDS.

Using Fluorescence-Activated Cell Sorting (FACS) analysis, monocyte/macrophage activation profiles will be characterized in patients within the first 24 hours after onset of ARDS and in matched mechanically ventilated controls. Markers of M1 ("pro-inflammatory") or M2 ("anti-inflammatory") activation, along with RAGE, TXNIP, NLRP3 FACS labeling in alveolar monocytes/macrophages will be analyzed along with protein measurements (IL-1β, TXNIP, NLRP3, sRAGE, HMGB1, S100A12) in the bronchoalveolar lavage fluid.

Study Timeline

• Study Start: 2015-09
• Study First Submitted: 2015-09-08
• Study First Submitted QC: 2015-09-08
• Study First Posted: 2015-09-10
• Status Verified: 2016-07
• Primary Completion: 2016-09
• Study Completion: 2016-10
• Last Update Submitted: 2020-05-09
• Last Update Posted: 2020-05-12

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• ICU patients without ARDS and under mechanical ventilation for less than 24 hours
• Patients within the first 24 hours after onset of moderate to severe ARDS according to the 2012 Berlin definition (ARDS group)

Exclusion Criteria

• • Pregnancy
• Acute exacerbation of diabetes (ketoacidosis, hyperosmolar hyperglycemic state)
• Patient under mechanical ventilation for > 7 days
• Dialysis-dependent chronic renal failure
• Alzheimer's disease
• Amyloidosis
• Evolutive neoplastic lesion
• Chronic pulmonary disease requiring long-term oxygen therapy or mechanical ventilation
• Chemotherapy treatment in the last 30 days
• Severe neutropenia (<0.5 G/l)

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
ARDS Group (acute respiratory distress syndrome)	RAGE TXNIP Inflammasome axis	The purpose of this monocentric observational prospective pathophysiology study is to compare alveolar monocyte/macrophage activation profiles between patients with or without ARDS
control group	RAGE TXNIP Inflammasome axis	The purpose of this monocentric observational prospective pathophysiology study is to compare alveolar monocyte/macrophage activation profiles between patients with or without ARDS

Primary Outcome Measures

Name	Time	Method
FACS analysis of RAGE-TXNIP-NLRP3 pathway in alveolar monocytes/macrophages	at day1	FACS analysis of RAGE-TXNIP-NLRP3 pathway in alveolar monocytes/macrophages from patients within the first 24 hours after onset of ARDS (ARDS group) and from sex- and age-matched mechanically ventilated controls (control group)

Secondary Outcome Measures

Name	Time	Method
- FACS analysis of M1 ("pro-inflammatory") and M2 ("anti-inflammatory") markers	at baseline	- FACS analysis of M1 ("pro-inflammatory") and M2 ("anti-inflammatory") markers (e.g., CD45, CD16, CD14, CD163, CD206, ICAM-1) in alveolar monocytes/macrophages from patients from both groups at baseline
IL-1β, TXNIP, NLRP3, sRAGE, HMGB1, S100A12 measurements	at baseline	- IL-1β, TXNIP, NLRP3, sRAGE, HMGB1, S100A12 measurements (duplicate ELISA) in the bronchoalveolar lavage fluid from patients from both groups at baseline

Trial Locations

Locations (1)

CHU Clermont-Ferrand; 🇫🇷 Clermont-Ferrand, France