Camu Camu in ART-treated People Living with HIV

NCT04058392 | Completed Phase 1 DMC

• 1 other identifier: CTNPT 032
• Study Type: interventional
• Target: 22
• Locations: 1 country
• Sites: 1

Brief Summary

Persons living with HIV and receiving antiretroviral therapy (ART) remain with inflammation leading to higher risks of cardiovascular diseases, fatty liver and cancer. It has been observed in colitis and in HIV infection that abnormal composition of the gut microbes and leaky gut induce inflammation contributing to diabetes, fatty liver and cardiovascular risks. Abundance of Akkermansia muciniphila in stool, a type of good bacteria acting as a shield on the gut barrier has been shown to prevent obesity, diabetes and to improve cancer treatment response. Health food (prebiotic) increases the frequency of A. muciniphila in overweight individuals. Dr Marette, a study collaborator from Laval University, has recently published (Gut, 2018) that an extract from a Brazilian fruit called Camu Camu (CC) protects mice from obesity, reduce LPS, a marker for passage of microbes from the gut into the blood and decreases inflammation in association with the frequency of A. muciniphila in stools. The extract of CC is sold in nutritional stores to regulate body fat. The investigators will invite 22 participants to take 2 capsules of CC daily for 12 weeks in addition to their ART. CC tolerance and changes in blood and stools for inflammation and microbe composition will be evalutated at the end of the 12-week treatment and 8 weeks post-intake. An optional sub study will assess the changes of gut barrier by doing biopsies by colonoscopy. CC is expected to beassociated with an enrichment of A. muciniphila in stools, combined with reduced gut damage and inflammation.

Conditions

HIV Infections

Outcome Measures

Primary Outcomes (1)

• Reduction of the plasma marker of microbial translocation LPS, assessed using ELISA.

  12 weeks

Secondary Outcomes (13)

• Safety and tolerability of CC

  20 weeks

• Changes in gut integrity markers I-FABP, and sST2, measured by ELISA

  12 weeks and 20 weeks

• Changes in microbial translocation marker 1-3-b-D-Glucan assessed using the Fungitell assay

  12 weeks and 20 weeks.

• Changes in pro-inflammatory markers (IL-1β, IL-6, IL-8, IL-18. IP-10, IL-17A and F, IL-22, and soluble CD14) and anti-inflammatory markers (IL-10) assessed by ELISA.

  12 weeks and 20 weeks

• Changes in T-cell and monocyte activation levels assessed by flow cytometry using markers CD38, HLA-DR and PD-1

  12 weeks and 20 weeks

Other Outcomes (2)

• Exploratory: Difference in HIV reservoir size from Baseline (Visit 0) to 12 weeks post-CC treatment by TILDA, performed on blood samples

  12 weeks

• Exploratory: Changes in other markers of gut damage (including plasma REG3α (45)), microbial translocation (such as plasma 16S rDNA) and immune activation (T-cell activation, cytokines) in the blood and gut biopsies.

  12 weeks

Study Arms (1)

Camu Camu

EXPERIMENTAL

Assessments will be done at baseline, during and after 12 weeks of Camu Camu intake.

Biological: Camu Camu Capsules

Interventions

Camu Camu Capsules BIOLOGICAL

Camu Camu powder encapsulated (500mg each). 2 capsules per day will be used for this study

Camu Camu

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Participants will be eligible for the study if they meet the following criteria:
• Male or female adults ≥18 years of age.
• Documented HIV-1 infection by Western Blot, Enzyme Immuno Assay (EIA) or viral load assay.
• On any ART for at least 2 years, with viremia less than 50 copies/ml during the last two years (occasional blips allowed).
• On a stable ART regimen (same prescription) for at least 3 months.
• CD4 count \>200 and a CD4/CD8 ratio \<1 suggesting an increase in inflammation and risk for non-AIDS events.
• Able to communicate adequately in either French or English.
• Able and willing to provide written informed consent prior to screening.
• Women of childbearing potential must have a negative serum pregnancy test.
• Women of childbearing potential must agree to use one of the following approved methods of birth control while in the study and until 2 weeks after completion:
• Complete abstinence from penile-vaginal intercourse from the screening period until two weeks after the study completion.
• Double barrier methods (acceptable barrier methods include diaphragm, coil, contraceptive foam, sponge with spermicide, condom); or
• Oral, injectable or implant contraceptives plus one barrier method;
• Intrauterine device (IUD) plus one barrier method; or
• Male partner sterilization confirmed prior to the female participant's entry into the study; this male is the sole partner for that participant.

You may not qualify if:

• Participants are not eligible to participate in the study if they meet any of the following conditions:
• Known allergy/hypersensitivity to Camu Camu.
• Current AIDS-related event or serious health condition including systemic infections in the last 3 months.
• Severe systemic diseases (e.g. uncontrolled hypertension, chronic renal failure), or active uncontrolled infections.
• Co-infection with active Hepatitis B or C Virus.
• Current use or have used in the past 3 months: immune-modulatory agents/chemotherapeutics, prophylactic antibiotics35/antibiotics, proton pump inhibitors, phosphate binders, Metformin or Morphine as these drugs can interact with vitamin C or modulate gut microbiota.
• Diagnosis of diabetes mellitus (HbA1c≥6.5%) as defined by the Canadian Clinical Practice Guidelines for the Prevention and Management of Diabetes42.
• Frequent use of polyphenol-rich prebiotics (e.g. cranberry and CC powders and/or capsules) in the last 12 months.
• Statin or other anti-cholesterol treatment use in the last 3 months.
• Recent changes in dietary habits, intermittent fasting, chronic constipation or laxative use as these can affect gut microbiota.
• Psychiatric or cognitive disturbance or any illness that could preclude compliance with the study.
• Current participation in an experimental therapy study or receipt of experimental therapy within the last 6 months.
• Women who are pregnant, planning to become pregnant, or breast-feeding.
• A score of higher than 8 on a Full AUDIT questionnaire (See Appendix 1) at the screening visit, suggesting an alcohol abuse problem.

Sponsors & Collaborators

• McGill University Health Centre/Research Institute of the McGill University Health Centre: lead

Study Sites (1)

Mcgill University Health Center

Montreal, Quebec, H4A 3J1, Canada

Location

Related Publications (5)

• Anhe FF, Nachbar RT, Varin TV, Trottier J, Dudonne S, Le Barz M, Feutry P, Pilon G, Barbier O, Desjardins Y, Roy D, Marette A. Treatment with camu camu (Myrciaria dubia) prevents obesity by altering the gut microbiota and increasing energy expenditure in diet-induced obese mice. Gut. 2019 Mar;68(3):453-464. doi: 10.1136/gutjnl-2017-315565. Epub 2018 Jul 31.

  PMID: 30064988 BACKGROUND

• Brenchley JM, Price DA, Schacker TW, Asher TE, Silvestri G, Rao S, Kazzaz Z, Bornstein E, Lambotte O, Altmann D, Blazar BR, Rodriguez B, Teixeira-Johnson L, Landay A, Martin JN, Hecht FM, Picker LJ, Lederman MM, Deeks SG, Douek DC. Microbial translocation is a cause of systemic immune activation in chronic HIV infection. Nat Med. 2006 Dec;12(12):1365-71. doi: 10.1038/nm1511. Epub 2006 Nov 19.

  PMID: 17115046 BACKGROUND

• Mehraj V, Jenabian MA, Ponte R, Lebouche B, Costiniuk C, Thomas R, Baril JG, LeBlanc R, Cox J, Tremblay C, Routy JP; Montreal Primary HIV Infection, the Canadian Long-Term Non-Progressors Study Groups. The plasma levels of soluble ST2 as a marker of gut mucosal damage in early HIV infection. AIDS. 2016 Jun 19;30(10):1617-27. doi: 10.1097/QAD.0000000000001105.

  PMID: 27045377 BACKGROUND

• Jenabian MA, El-Far M, Vyboh K, Kema I, Costiniuk CT, Thomas R, Baril JG, LeBlanc R, Kanagaratham C, Radzioch D, Allam O, Ahmad A, Lebouche B, Tremblay C, Ancuta P, Routy JP; Montreal Primary infection and Slow Progressor Study Groups. Immunosuppressive Tryptophan Catabolism and Gut Mucosal Dysfunction Following Early HIV Infection. J Infect Dis. 2015 Aug 1;212(3):355-66. doi: 10.1093/infdis/jiv037. Epub 2015 Jan 23.

  PMID: 25616404 BACKGROUND

• Isnard S, Fombuena B, Ouyang J, Royston L, Lin J, Bu S, Sheehan N, Lakatos PL, Bessissow T, Chomont N, Klein M, Lebouche B, Costiniuk CT, Routy B, Marette A, Routy JP; Camu Camu Study Group. Camu Camu effects on microbial translocation and systemic immune activation in ART-treated people living with HIV: protocol of the single-arm non-randomised Camu Camu prebiotic pilot study (CIHR/CTN PT032). BMJ Open. 2022 Jan 17;12(1):e053081. doi: 10.1136/bmjopen-2021-053081.

  PMID: 35039291 DERIVED

MeSH Terms

Conditions

HIV Infections

Condition Hierarchy (Ancestors)

Blood-Borne Infections; Communicable Diseases; Infections; Sexually Transmitted Diseases, Viral; Sexually Transmitted Diseases; Lentivirus Infections; Retroviridae Infections; RNA Virus Infections; Virus Diseases; Genital Diseases; Urogenital Diseases; Immunologic Deficiency Syndromes; Immune System Diseases

Study Officials

• Jean-Pierre Routy, MD

  McGill University Health Centre/Research Institute of the McGill University Health Centre

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Professor

Study Record Dates

• First Submitted: May 6, 2019
• First Posted: August 15, 2019
• Study Start: November 9, 2020
• Primary Completion: July 20, 2022
• Study Completion: July 20, 2022
• Last Updated: November 20, 2024

Record last verified: 2024-11

Data Sharing

• IPD Sharing: Will not share

Locations

CA (1)