Synbiotic therapy decreases microbial translocation and inflammation and improves immunological status in HIV-infected patients: a double-blind randomized controlled pilot trial

Nutr J. 2012 Oct 29:11:90. doi: 10.1186/1475-2891-11-90.

Abstract

Background: HIV-infection results in damage and dysfunction of the gastrointestinal system. HIV enteropathy includes pronounced CD4+ T-cell loss, increased intestinal permeability, and microbial translocation that promotes systemic immune activation, which is implicated in disease progression. A synbiotic is the combination of probiotics and prebiotics that could improve gut barrier function. Our study goal was to determine whether the use of a synbiotic, probiotics or a prebiotic can recover immunological parameters in HIV-infected subjects through of a reduction of microbial translocation and pro-inflammatory cytokine production.

Methods: A randomized, double-blind controlled study was performed; twenty Antiretroviral treatment-naïve HIV-infected subjects were subgrouped and assigned to receive a synbiotic, probiotics, a prebiotic, or a placebo throughout 16 weeks.

Results: We had no reports of serious adverse-events. From baseline to week 16, the synbiotic group showed a reduction in bacterial DNA concentrations in plasma (p = 0.048). Moreover, the probiotic and synbiotic groups demonstrated a decrease in total bacterial load in feces (p = 0.05). The probiotic group exhibited a significant increment of beneficial bacteria load (such as Bifidobacterium; p = 0.05) and a decrease in harmful bacteria load (such as Clostridium; p = 0.063). In the synbiotic group, the CD4+ T-cells count increased (median: +102 cells/μL; p = 0.05) and the level of Interleukin 6 cytokine decreased significantly (p = 0.016).

Conclusions: Our study showed a significant increase in CD4+ T lymphocyte levels in the synbiotic group, which could delay the initiation of antiretroviral therapy and decrease costs in countries with limited resources.

Publication types

  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Anti-Inflammatory Agents, Non-Steroidal / adverse effects
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use*
  • Bacterial Translocation*
  • Bifidobacterium / classification
  • Bifidobacterium / growth & development
  • Bifidobacterium / immunology
  • Bifidobacterium / isolation & purification
  • CD4 Lymphocyte Count
  • Cytokines / blood
  • Cytokines / metabolism
  • DNA, Bacterial / blood
  • Disease Progression
  • Double-Blind Method
  • Feces / microbiology
  • Female
  • HIV Enteropathy / diet therapy*
  • HIV Enteropathy / immunology
  • HIV Enteropathy / microbiology
  • HIV Enteropathy / physiopathology
  • Humans
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / microbiology*
  • Intestinal Mucosa / physiopathology
  • Lacticaseibacillus rhamnosus / classification
  • Lacticaseibacillus rhamnosus / growth & development
  • Lacticaseibacillus rhamnosus / immunology
  • Lacticaseibacillus rhamnosus / isolation & purification
  • Male
  • Mexico
  • Pilot Projects
  • Prebiotics* / adverse effects
  • Probiotics* / adverse effects
  • Probiotics* / isolation & purification
  • Quality of Life
  • Young Adult

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Cytokines
  • DNA, Bacterial
  • Prebiotics