MetACTIVIH: Immune Activation as a Cause of Insulin Resistance in Adults Living With HIV-1 on Effective Antiretroviral Therapy

Sponsor
University Hospital, Montpellier (Other)
Overall Status
Recruiting
CT.gov ID
NCT04028882
Collaborator
(none)
300
1
35.9
8.4

Study Details

Study Description

Brief Summary

The aim of this study is to characterize in non-viremic HIV-1 patients under antiretroviral therapy an immune activation profile that the investigators have previously shown to be strongly linked to hyperinsulinemia. This characterization will be carried out via 3 different approaches. First, the investigators will analyze the metabolites present in the plasma of patients presenting with the profile of interest. Second, the investigators will study the transcriptome of the peripheral blood mononuclear cells of these patients. Finally, the investigators will search whether some factors released by these cells are able to induce insulin resistance. In addition the ability of the profile of interest to predict an increase in insulinemia over time will be assessed.

Condition or Disease Intervention/Treatment Phase
  • Other: Signaling, metabolomic and transcriptomic analysis

Detailed Description

The working hypothesis of this study is that in efficiently treated HIV patients, various profiles of immune activation may be distinguished, each favouring particular comorbidities. Using a panel of 68 soluble and cell surface markers, the investigators have previously measured the level of activation in circulating Cluster of Differentiation 4+ (CD4+) and Cluster of Differentiation 8+ (CD8+), T cells, B cells, monocytes, Natural Killers (NK) cells, neutrophils, and endothelial cells as well as of inflammation and fibrinolysis in 120 virologic responders over 45 years of age. Two independent hierarchical clustering analyses allowed the investigators to identify five patient groups, each with the same activation profile. One of these profiles, Profile#2, was strongly associated with hyperinsulinemia (Psomas et al., 2016).

The main objective of the present study is to better define Profile#2. To this aim, the investigators will analyze by mass spectrometry the metabolites in the plasma of patients with various profiles including the one of interest. Concurrently, the investigators will perform an RiboNucleic Acid Sequencing (RNASeq) analysis on peripheral blood mononuclear cells (PBMC) from the same patients. These metabolomic and transcriptomic data will help to better define the immune activation profiles.

The secondary objective is to test whether the link the investigators have observed between Profile#2 and insulin resistance is causative. To this aim, by following over time patients' insulinemia, the investigators will test whether Profile#2 is predictive of an increase in insulinemia. The investigators will also look for factors released by PBMC of patients with Profile#2 able to induce insulin resistance.

Study Design

Study Type:
Observational
Anticipated Enrollment :
300 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Immune Activation as a Cause of Insulin Resistance in Adults Living With HIV-1 on Effective Antiretroviral Therapy
Actual Study Start Date :
Mar 3, 2020
Anticipated Primary Completion Date :
Mar 1, 2023
Anticipated Study Completion Date :
Mar 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Non viremic HIV patients under treatment

Patients with various immune activation profiles

Other: Signaling, metabolomic and transcriptomic analysis
Signaling, metabolomic and transcriptomic analysis

Outcome Measures

Primary Outcome Measures

  1. Metabolomic analysis on plasma and PBMC [18 months]

    The investigators will analyze by mass spectrometry the metabolites present in the plasma of patients presenting with the profile of interest as compared with patients with other immune activation profiles. Metabolites will be extracted from the blood plasma using a salt assisted liquid-liquid extraction. The metabolites will then be allowed to crystallize on the metallic surface. Finally, the plate content will be analyzed by desorption electrospray ionisation mass spectrometry using positive and negative ionization.

  2. Transcriptomic analysis on plasma and PBMC [18 months]

    The investigators will also analyze by RNASeq the messenger RNA (mRNA) produced by the PBMC of patients presenting with the profile of interest and compared them with the mRNA produced by the PBMC of patients with other immune activation profiles.

Secondary Outcome Measures

  1. Follow-up over time of insulinemia in patients with various immune activation profiles [18 months]

    The investigators will compare over time the increase in insulinemia in patients presenting or not the immune activation profile of interest.

  2. Test whether PBMC from patients with Profile#2 induce insulin resistance [18 months]

    The investigators will analyze whether PBMC from patients with the immune activation profile of interest release factors able to inhibit insulin signaling in hepatocytes. Insulin signaling will be measured by quantifying Akt phosphorylation vie western blot.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion criteria:
  • Subject consulting or hospitalized in the tropical and infectious diseases unit at the University Hospital of Montpellier that have been enrolled in a study during which the immune activation profile was analyzed

  • Subject aged at least 18 years

  • Subject speaking french fluently

  • Subject who is not opposed to participate to the study, after a clear information

  • Subject affiliated to a social security system

  • Infection by HIV-1 determined by a positive serology or by a measure of the plasma viral load (RNA HIV)

  • HIV-1 patients under stable antiretroviral therapy

  • HIV load < 50 copies/mL since at least 6 months before enrollment (2 measures)

Exclusion criteria:
  • Vulnerable individuals

  • Persons protected

  • Pregnant women or breastfeeding mothers

  • Bad understanding of the nature and goals of the study and/or communication difficulties with the investigator

  • Subject enrolled in an other study with an exclusion period still running

  • Non infectious pathology that might be the origin of an immune anomaly

  • Treatment by an immune modulator molecule or by chemotherapy in the 60 days before enrollment in the study

Contacts and Locations

Locations

Site City State Country Postal Code
1 Saint Eloi Hospital, University Hospital of Montpellier Montpellier Hérault France 34295

Sponsors and Collaborators

  • University Hospital, Montpellier

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University Hospital, Montpellier
ClinicalTrials.gov Identifier:
NCT04028882
Other Study ID Numbers:
  • RECHMPL18_0373
First Posted:
Jul 23, 2019
Last Update Posted:
Feb 12, 2021
Last Verified:
Feb 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 12, 2021