Modern antiretroviral therapy (ART) has transformed the clinical care and lived experience of HIV infection. However, increased rates of adverse health conditions that are related to immune activation, such as cardiovascular disease (CVD) and neurodegenerative disease in ART-treated individuals persist. An important cause of this inflammation is the gut CD4 T cell loss and the "leaking" or translocation of luminal gut bacteria and other microbes across the bowel wall and into the bloodstream. The use of complementary and alternative therapies is very common among people living with HIV, with estimates ranging from 16-60%. However, their efficacy has generally not been well demonstrated. Probiotics are live microbes that may provide a health benefit to the host and the investigators believe that the simultaneous use of probiotics along with ART will improve gut CD4 T cell restoration and function and therefore reduce microbial translocation and immune activation. A major challenge to HIV treatment is the suboptimal CD4 T cell count despite successful HIV suppression on ART in immunologic non-responders (INRs). These individuals are at increased risk of AIDS-related deaths and non-AIDS related comorbidities that may be associated with increased immune activation and microbial translocation from the gut mucosa. With limited treatment options, alternative therapies to reduce inflammation and restore gut immunology will be important. Probiotic Visbiome consists of a high potency blend of eight different probiotics. The precise mechanism of action of Visbiome is unknown,but preclinical studies have shown that Visbiome may modulate the immune response towards an immunoregualtory phenotype with increased the levels of IL-10 and reduced levels of proinflammatory cytokines (TNFα, IL1β and IL-8). Therefore,the investigators believe that the "beneficial" bacteria from Visbiome will accelerate the normalization of gut immune cells and function in HIV-infected INRs. It is hypothesized consumption of Visbiome for 48 weeks will help restore the immune system in INRs who have suboptimal immune reconstitution to currently available ART. Resolution of gut immune cells will mean that microbial translocation and immune activation will be normalized and will reduce the rates of HIV-associated comorbidities.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
36
Maple Leaf Medical Clinic
Toronto, Ontario, Canada
RECRUITINGToronto General Hospital, UHN
Toronto, Ontario, Canada
RECRUITINGPercent change in blood immune activation
Percent change in blood immune activation (co-expression of CD38 and HLA-DR) on CD8 T cells at week 48 in participants randomized to probiotic Visbiome versus the placebo arm
Time frame: 48 weeks
Level of microbial translocation (including LSP and sCD14)
Time frame: 48 weeks
Plasma level of inflammation and coagulation (including IL-6, D-dimer and CRP)
Time frame: 48 weeks
Number and function of gut immune cells (including CD4 T cell subsets)
Time frame: 48 weeks
Intestinal permeability (Lac/Mac ratio)
Time frame: 48 weeks
Bacterial community diversity, determined by 16s rRNA gene sequencing of penile swabs
Time frame: 48 weeks
Bacterial community composition, determined by 16s rRNA gene sequencing of penile swabs
Time frame: 48 weeks
Gut HIV DNA levels
Time frame: 48 weeks
Canadian Diet History Questionnaire
Time frame: 48 weeks
Safety assessed by AE monitoring and participant questionnaire
Time frame: 48 weeks
Tolerability of Visbiome assessed by AE monitoring and participant questionnaire
Time frame: 48 weeks
Adherence to Visbiome assessed by participant questionnaire and sachet count
Time frame: 48 weeks
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