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Gut Microbiota Changes of HIV Patients Before and After One Year of ART

Completed
Conditions
HIV Infections
Interventions
Drug: Antiretroviral Therapy
Registration Number
NCT04297501
Lead Sponsor
Peking Union Medical College Hospital
Brief Summary

HIV infection leads to destruction of CD4+T cells in the gut-associated lymphoid tissue (GALT) and promotes a decline in mechanical barrier functions of the gut mucosa, and the subsequent translocation of microbial products from the gastrointestinal tract to systemic circulation. The gut mucosal immune system is not completely restored by cART, and the resultant microbial translocation may contribute to chronic inflammation, inadequate CD4 T-cell recovery, and increased rates of serious non-AIDS events. Many studies have revealed strong and characteristic compositional differences in gut microbiota between individuals with HIV infection and seronegative controls. So far, several probiotic organisms have shown the ability to enhance intestinal epithelial barrier functions, reduce inflammation, and support effective Th-1 responses. Probiotics mainly stimulates polymeric IgA secretion, avoid bacterial overgrowth and their translocation, and produce a self-limited inflammatory response through development of regulatory T (Treg) cells by anti-inflammatory cytokine production. Therefore, we design a prospective, randomized, double-blind, placebo-controlled study to determine whether the use of a probiotic can expand beneficial microbiota that aid in decreasing bacterial translocation and pro-inflammatory cytokine production, thereby improving immune functions in HIV-infected subjects. Participants in the intervention group will receive oral probiotic containing 3 billion Bifidobacterium and 1 billion Lactobacillus once daily, while those in the placebo group will take placebo which contains no probiotic but has the same flavor and characteristics as the probiotic product.. Gut bacterial community diversity and composition, immune recovery and activation in peripheral plasma, plasma levels of gut damage, microbial translocation and inflammation at baseline and after 12 months of receiving intervention will be analyzed.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
50
Inclusion Criteria
  • 18-65 years old;
  • Documented HIV infection;
  • No history of gastrointestinal diseases;
  • Good adherence and promise to follow-up;
  • Ability to provide informed consent.
Exclusion Criteria
  • Administration of antibiotics, probiotics, or prebiotics or experience of diarrhea within the previous 3 months;
  • Administration of anti-inflammatory drugs, corticosteroids, immunosuppressive drugs, immunomodulator within the previous 3 months;
  • Severe organ dysfunction;
  • Pregnancy or breastfeeding.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
All participantsAntiretroviral TherapyAll enrolled participants in this study
Primary Outcome Measures
NameTimeMethod
Gut bacterial community diversity and compositionChange from baseline to 1 year after antiretroviral therapy

Microbiota profiling are performed on fecal samples from each subjects, and 8-10 participants receive gastrointestinal endoscope according to their willingness

Secondary Outcome Measures
NameTimeMethod
Plasma levels of inflammation and coagulation markersChange from baseline to 1 year after antiretroviral therapy

Levels of IL-8, IL-1β, IL-6, CRP, TNF-α and D-dimer

Feasibility, safety, tolerability, adherence, and acceptability of study product and proceduresChange from baseline to 1 year after antiretroviral therapy

Based on patients' description and intervention-related adverse events

Absolute CD4+ T-cell and CD8+ T-cell counts in peripheral plasmaChange from baseline to 1 year after antiretroviral therapy

CD4+ and CD8+ T cells are analyzed by flow cytometry

The level of T cell activation and different immunophenotype in peripheral plasmaChange from baseline to 1 year after antiretroviral therapy

CD38+HLA-DR+, CD8+CD28+ T cell subsets are analyzed by flow cytometry

Metabolic measurements from blood plasmaChange from baseline to 1 year after antiretroviral therapy

Levels of vitamin D, glucose and insulin, and lipid profiling

Plasma levels of microbial translocation and monocyte activation markersChange from baseline to 1 year after antiretroviral therapy

Levels of I-FABP, LPS, LBP, sCD14, sCD40L, and IDO

HIV RNAChange from baseline to 1 year after antiretroviral therapy

HIV-RNA is detected by Roche assay with the limit of 20 copies/mL

Trial Locations

Locations (1)

Peking Union Medical College Hospital

🇨🇳

Beijing, China

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