Exploratory Study on the Role of the Digestive Microbiota in Adults Living With HIV-1

HIV Clinical Trial

— MICRACTIVIH  

Official title:

Exploratory Study on the Role of the Digestive Microbiota and Bacterial Translocation in the Immune Activation Profile Associated With Insulin Resistance in Male Caucasian Adults Living With HIV-1 on Effective Antiretroviral Therapy.

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT05724524
• Other study ID #: AOI GCS-MERRI/2019/JPL-01
• Status: Withdrawn
• Start date: May 2022
• Est. completion date: February 2023

Study information

• Verified date: February 2023
• Source: Centre Hospitalier Universitaire de Nimes
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Chronic immune activation present in aviremic people living with HIV under treatment promotes the onset of insulin resistance and metabolic syndrome, paving the way for the comorbidities that are currently the main causes of morbidity. This activation continues despite effective antiretroviral therapy. In the ACTIVIH study (NCT02334943) the analysis of 68 AI markers allowed classification of 120 aviremic PLHIV under treatment for at least 2 years according to 5 different immune activation profiles. Among these 5 profiles, Profile 2 was characterized by high blood pressure figures, high waist sizes, low HDL-cholesterol levels, high triglyceridemia, and especially hyperinsulinemia. Several studies have shown that the digestive microbiota of this population is less rich and less diverse than that of healthy subjects. However, the digestive microbiota and in particular bacterial proteins and metabolites seem to play a key role in immune activation in people living with HIV. Finally, the digestive microbiota has already been shown to have an impact on insulin sensitivity.

The study investigators hypothesize that a particular digestive microbiota could promote the appearance of Profile 2. This microbiota could be the cause of digestive dysbiosis leading to intestinal inflammation, digestive permeability and bacterial translocation.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: February 2023
• Est. primary completion date: February 2023
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patient informed of the implementation of the study, its objectives, its constraints and the patient's rights.

• Male and Caucasian patient.

• Patient with HIV-1 infection determined by positive serology or plasma viral load (HIV RNA) measurement.

• Patient on effective triple antiretroviral therapy, stable for more than 6 months, with a plasma viral load <50 copies / ml for at least 6 months before inclusion (2 measurements).

• Patient whose immune activation profile has been characterized beforehand (profiles 1, 2, 3, 4 and 5).

• The patient must have given their free and informed consent and signed the consent form

• The patient must be a member or beneficiary of a health insurance plan

Exclusion Criteria:

• Vulnerable person according to article L1121-6 of the CSP.

• Adult person protected according to article L1121-8 of the CSP.

• Patient presenting with a non-infectious pathology which may be the cause of an immune abnormality.

• Patient having undergone treatment with an immunomodulator molecule or chemotherapy within 60 days before inclusion in the research or has an indication planned for the duration of the research.

• Patient with a chronic digestive pathology or who had been operated on the previous year

• The subject is participating in a category 1 interventional study, has participated in another interventional study in the last 3 months or is in a period of exclusion determined by a previous study

• The subject refuses to sign the consent

• It is impossible to give the subject informed information

• The patient is under safeguard of justice or state guardianship

Related Conditions & MeSH terms

• HIV

Intervention

Other:
• Stool sample collection
50mg stool sample taken for protein extraction
• Blood sample collection
Venous blood sample taken for analysis of serum and plasma

Locations

Country	Name	City	State
France	CHU Gui de Chauliac	Montpellier
France	CHU de Nîmes	Nîmes

Sponsors (1)

Lead Sponsor	Collaborator
Centre Hospitalier Universitaire de Nimes

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Nature of gut microbiota bacterial proteins in patients with immune activation profile 2 versus all other profiles	Number of bacterial proteins present in stool samples from patients, identified by high-performance liquid chromatography mass spectrometry	Day 0
Primary	Nature of gut microbiota taxonomy in patients with immune activation profile 2 versus all other profiles	Number of operational taxonomic units present in stool samples from patients, identified by high-performance liquid chromatography mass spectrometry	Day 0
Primary	Relative quantification of gut microbiota bacterial proteins in patients with immune activation profile 2 versus all other profiles	Percentage of the various bacterial proteins present in stool samples from patients, identified by high-performance liquid chromatography mass spectrometry (%)	Day 0
Primary	Relative quantification of gut microbiota taxonomy in patients with immune activation profile 2 versus all other profiles	Percentage of the various operational taxonomic units present in stool samples from patients, identified by high-performance liquid chromatography mass spectrometry (%)	Day 0
Secondary	Richness of Firmicutes and Bacteroidetes in patients with immune activation profile 2 versus all other profiles	Rarefaction curves	Day 0
Secondary	Diversity of Firmicutes and Bacteroidetes in patients with immune activation profile 2 versus all other profiles	Shannon index	Day 0
Secondary	beta-diversity of Firmicutes and Bacteroidetes in patients with immune activation profile 2 versus all other profiles	Unifrac	Day 0
Secondary	Level of phyla and minority species in the stool in patients with immune activation profile 2 versus all other profiles	high-performance liquid chromatography mass spectrometry	Day 0
Secondary	Level of CD14S in serum of patients with immune activation profile 2 versus all other profiles	ng/ml by ELISA	Day 0
Secondary	Level of Lipopolysaccharide Binding Protein (LBP) in serum of patients with immune activation profile 2 versus all other profiles	pg/ml by ELISA	Day 0
Secondary	Level of intestinal fatty acid binding protein (I-FABP) in serum of patients with immune activation profile 2 versus all other profiles	ng/ml by ELISA	Day 0
Secondary	Level of bacterial 16S rDNA in plasma of patients with immune activation profile 2 versus all other profiles	Copies/µl	Day 0
Secondary	Transcriptomic analysis of peripheral blood mononuclear cells	RNAseq	Day 0