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Beta-Glucan Study

Pilot study into effects of oral yeast beta-glucan supplement with zinc and selenium (ABB C1©) on trained immunity responses and gut integrity in people living with HIV - Beta-Glucan Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON57927
Enrollment
50
Registered
2025-04-14
Start date
2025-11-28
Completion date
Unknown
Last updated
2026-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV, gut barrier function, systemic inflammation, functional immunology Immunity and intestinal inflammation

Interventions

The ABB C1®&nbsp
dietary supplement is based on S. cerevisiae&nbsp
with added sweeteners. Each sachet contains 233 mg S. cerevisiae&nbsp
mineral yeast and 517 mg S. cerevisiae&nbsp
beta-glucans. Placebo consists of mainly mannitol and maltodextrin in the exact same form as the ABB C1® supplement. Participants will consume one stick daily with food or drink for 6 weeks.&nbsp

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Adult cis-gender males above 18 years of ageDocumented HIV-1 infectionon cART =6 months HIV-RNA load <40 copies/mL in latest measurement Latest CD4+ T-cell count = 200 cells/mm3 in latest measurementBeing participant of 2000HIV studyThe control subjects without HIV should be cis-gender males above 18 years of age. 

Exclusion criteria

Exclusion criteria: No informed consentInsufficient communication because of language or other problemsActive hepatitis B/C or signs of acute infections or other acute conditionsOral antibiotics use in the past 3 monthsVaccination in the month prior to inclusion, or planned vaccination during course of the study Use of other prebiotic or probiotic supplementationUse of systemic anti-inflammatory or immunomodulatory drugs, such as biologics or corticosteroids

Design outcomes

Primary

MeasureTime frame
The main study parameters of this study include whole blood hemocytometer data, ex vivo cytokine production by peripheral blood mononuclear cells (PBMCs) upon stimulation with a panel of stimuli,  Olink plasma proteomics for circulating inflammatory and gut barrier function markers, and fecal calprotectin levels. 

Secondary

MeasureTime frame
Beta-glucan level in blood; neutrophil activation, ROS production and killing capacity

Countries

Netherlands

Contacts

Public ContactTJW Otten

Radboud Universitair Medisch Centrum

twanotten@gmail.com0243611111

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jul 23, 2026