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The Effect of Probiotics in HIV-1 Infection (ProGut)

Primary Purpose

HIV-1 Infection

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Multi-strain probiotic
Placebo
Sponsored by
Oslo University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV-1 Infection focused on measuring HIV, microbial translocation, immune activation, probiotics

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • For patients without ART: Confirmed diagnosis of HIV infection > 6 months and CD4+ T cell count < 900
  • For patients on stable, effective ART: HIV RNA < 50 copies/ml > 6 months and CD4+ T cell count > 500
  • Signed informed consent.

Exclusion Criteria:

  • Severe illness requiring hospitalization
  • Systemic antibiotics or probiotics the last two months
  • Current immune modulating therapy
  • Infectious diarrhea
  • Inflammatory bowel disease
  • Acute primary HIV infection
  • Patients immigrating from Africa, Asia or Latin-America within the last 6 months.

Sites / Locations

  • Oslo University Hospital
  • Karolinska University Hospital Huddinge

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Placebo Comparator

No Intervention

Arm Label

Probiotics

Placebo

Control

Arm Description

A multi-strain Probiotic consisting of Lactobacillus rhamnosus GG, Lactobacillus acidophilus La-5 and Bifidobacterium animalis subsp. lactis Bb-12 added to fermented skimmed milk (Biola®, TINE SA, Oslo), 250 mL/day for 8 weeks.

Fermented and subsequently heat-treated, sterile skimmed milk (TINE SA) as active placebo.

No intervention

Outcomes

Primary Outcome Measures

Safety
Adverse events monitoring during the study period of 2 months
Changes in measures of microbial translocation
Changes in plasma leves of lipopolysaccharide (LPS) and soluble CD14 from baseline to 2 months (end of study)
Changes in markers of immune activation
Changes in CD38, HLA-DR and PD-1 on CD8+ and CD4+ T cells from baseline to 2 months (end of study)

Secondary Outcome Measures

Disease progression in untreated patients
Changes in CD4 count, viral load, clinical events and indication for ART from baseline to 2 months (end of study)
Immune reconstitution in ART treated patients
Changes in CD4 count from baseline to 2 months (end of study)
Gut microbiota composition
Changes in gut microbiota (454 pyrosequencing of fecal samples) from baseline to 2 months (end of study)

Full Information

First Posted
September 16, 2011
Last Updated
September 26, 2017
Sponsor
Oslo University Hospital
Collaborators
Karolinska University Hospital, Tine
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1. Study Identification

Unique Protocol Identification Number
NCT01439841
Brief Title
The Effect of Probiotics in HIV-1 Infection
Acronym
ProGut
Official Title
The Effect of Probiotics on Microbial Translocation and Immune Activation in HIV-1 Infection. A Randomised Placebo-controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2017
Overall Recruitment Status
Completed
Study Start Date
October 2011 (undefined)
Primary Completion Date
April 2013 (Actual)
Study Completion Date
June 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oslo University Hospital
Collaborators
Karolinska University Hospital, Tine

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
HIV progression is closely associated with chronic immune activation driven by leakage of bacterial products from a damaged gut, the investigators largest immunological organ. Notably, the degree of immune activation has been suggested to be a better predictor of disease progression than plasma viral load, and markers of immune activation and gut damage have been identified as therapeutic targets per se. The major damage by HIV to the immune system is an initial massacre of gut mucosal CD4+ Th17 cells. Interestingly, a normal gut flora has been shown to induce the maturation of Th17 cells in the small intestine mucosa. Preliminary reports have shown that the gut flora is altered in HIV-1 infection compared to controls. In this project, the investigators will characterize microbial composition of gut flora in chronic HIV infection with ultradeep sequencing. Gut flora composition will be related to clinical data as well as quantitative data of circulating microbial products and activation markers. Second, in a randomized clinical trial (RCT) the effect of probiotic lactobacilli on HIV pathogenesis and progression will be tested. This Gram-positive strain is clinically tested and is able to colonize the gut.
Detailed Description
Objectives: To explore (i) the safety and tolerability, and (ii) the efficacy of probiotics on HIV-associated microbial translocation, systemic immune activation, disease progression and composition of gut microbiota in chronic HIV-1 infection. Methodology/Study design: Approximately 50 patients without current indication for antiretroviral treatment (ART) and 50 patients receiving ART without normalised CD4 counts will be included. A controlled clinical trial will be carried out within each stratum randomised in a 2:1:1 fashion to double blinded intervention and placebo arms as well as an open, untreated control arm, respectively.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV-1 Infection
Keywords
HIV, microbial translocation, immune activation, probiotics

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Probiotics
Arm Type
Experimental
Arm Description
A multi-strain Probiotic consisting of Lactobacillus rhamnosus GG, Lactobacillus acidophilus La-5 and Bifidobacterium animalis subsp. lactis Bb-12 added to fermented skimmed milk (Biola®, TINE SA, Oslo), 250 mL/day for 8 weeks.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Fermented and subsequently heat-treated, sterile skimmed milk (TINE SA) as active placebo.
Arm Title
Control
Arm Type
No Intervention
Arm Description
No intervention
Intervention Type
Dietary Supplement
Intervention Name(s)
Multi-strain probiotic
Other Intervention Name(s)
Brand name Biola®
Intervention Description
The product consists of Lactobacillus rhamnosus GG, Lactobacillus acidophilus La-5 and Bifidobacterium animalis subsp. lactis Bb-12 added to fermented skimmed milk
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Fermented and subsequently heat-treated, sterile skimmed milk
Primary Outcome Measure Information:
Title
Safety
Description
Adverse events monitoring during the study period of 2 months
Time Frame
2 months
Title
Changes in measures of microbial translocation
Description
Changes in plasma leves of lipopolysaccharide (LPS) and soluble CD14 from baseline to 2 months (end of study)
Time Frame
2 months
Title
Changes in markers of immune activation
Description
Changes in CD38, HLA-DR and PD-1 on CD8+ and CD4+ T cells from baseline to 2 months (end of study)
Time Frame
2 months
Secondary Outcome Measure Information:
Title
Disease progression in untreated patients
Description
Changes in CD4 count, viral load, clinical events and indication for ART from baseline to 2 months (end of study)
Time Frame
2 months
Title
Immune reconstitution in ART treated patients
Description
Changes in CD4 count from baseline to 2 months (end of study)
Time Frame
2 months
Title
Gut microbiota composition
Description
Changes in gut microbiota (454 pyrosequencing of fecal samples) from baseline to 2 months (end of study)
Time Frame
2 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: For patients without ART: Confirmed diagnosis of HIV infection > 6 months and CD4+ T cell count < 900 For patients on stable, effective ART: HIV RNA < 50 copies/ml > 6 months and CD4+ T cell count > 500 Signed informed consent. Exclusion Criteria: Severe illness requiring hospitalization Systemic antibiotics or probiotics the last two months Current immune modulating therapy Infectious diarrhea Inflammatory bowel disease Acute primary HIV infection Patients immigrating from Africa, Asia or Latin-America within the last 6 months.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Geir Gokstad, MD, PhD
Organizational Affiliation
Oslo University Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Marius Trøseid, MD, PhD
Organizational Affiliation
Oslo University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Oslo University Hospital
City
Oslo
ZIP/Postal Code
0407
Country
Norway
Facility Name
Karolinska University Hospital Huddinge
City
Stockholm
ZIP/Postal Code
14186
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
26258571
Citation
Stiksrud B, Nowak P, Nwosu FC, Kvale D, Thalme A, Sonnerborg A, Ueland PM, Holm K, Birkeland SE, Dahm AE, Sandset PM, Rudi K, Hov JR, Dyrhol-Riise AM, Troseid M. Reduced Levels of D-dimer and Changes in Gut Microbiota Composition After Probiotic Intervention in HIV-Infected Individuals on Stable ART. J Acquir Immune Defic Syndr. 2015 Dec 1;70(4):329-37. doi: 10.1097/QAI.0000000000000784.
Results Reference
derived

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The Effect of Probiotics in HIV-1 Infection

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