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NCT Number: NCT05313451

Evaluation of the Effect of a Soluble Fiber Consumption on Immunity Response

At European level, the European Food Safety Agency has recognized two claims relating to the effects of prebiotics on the gastrointestinal sphere and on the immune system. In subjects aged 45-63, it was shown that a pre- and post-vaccination inulin consumption of 8g/day significantly increased the titer of antibodies directed against the H3N2 viral strain. The increase in bifidobacteria in the faeces confirmed that this effect was related to prebiotic capacities. The effect of prebiotics and probiotics on the immune response to influenza virus vaccination has been studied in two systematic reviews and meta-analyses. The authors show that the consumption of prebiotic fibers such as FOS, GOS, inulin, was also effective on the H3N2 strain, as on the H1N1 and B strains (antibody titers of 19.5%, 20.0% and 13.6% higher, respectively, compared to placebo).

The soluble fiber under study is a resistant dextrin meeting the definition of a prebiotic fibre. The prebiotic properties have been demonstrated in humans in several studies for doses ranging from 10 to 20 g/day. Similarly, studies show that the effects on immune functions are favorably impacted by a consumption of 10 g/day for 8 weeks . These results confirm those of a preclinical study conducted in mini-pigs.

The main objective of these study is to demonstrate that these prebiotic properties could help stimulate the post-vaccination immune response, and more specifically the production of antibodies directed against seasonal influenza viruses (following vaccination), and modulate the pro- and anti-inflammatory responses.

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Key information

Conditions

Immune Response

Age range

50 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CEN Nutriment

Dijon, Bourgogne-Franche-Comté, 21000, France

About this study

Screened participants who met the eligibility criteria are randomized either in the control or test (soluble fiber) group.

They are asked to ingest placebo or test product at 15 g/d dosing for 60 days (2 months) . At the end of the first month (30 days) they get vaccinated against influenza virus. The effect of soluble fiber on immune response is assessed by the comparison of HI titration 30 days after vaccination between groups.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Main Inclusion Criteria:

  • Subject with a body mass index (BMI) of 18.0-30.0 kg/m 2
  • Subject with regular upper respiratory tract infections(nasopharyngitis, flu-like illness, flu, cold...)
  • Subject accepting the anti-influenza virus vaccination
  • Subject agreeing to maintain lifestyle and dietary habits over the study

Main Exclusion Criteria:

  • Subject having had the flu during the current season
  • Subject having presented a viral or bacterial infection in the past 7 days prior to inclusion
  • Subject with a known allergy to one of the compounds of products administered in the study or in accordance with indications of the vaccine
  • Subject having presented manifestations of allergy during previous flu vaccinations
  • Subject with ongoing gastrointestinal disease or chronic gastrointestinal disease (IBS, Crohn's disease, etc.)
  • Suffering from diabetes, an autoimmune disease, a disease inflammation or a major or progressive pathology
  • Pregnant women (negative urine pregnancy test for women of childbearing age), breastfeeding or planning a pregnancy in the coming months
  • Subject who has already received the influenza vaccine for the current season
  • Subject having received any vaccination during the last month prior to inclusion
  • Subject who received antibiotic therapy within the last two month
  • Taking any dietary supplements or enriched foods that are presented as having an action on immunity and/or on the intestinal sphere (prebiotics, probiotics, vitamins, plant extracts...) in the last month.
  • Taking immunomodulatory or immunosuppressive drugs
  • Taking any treatment that the investigator believes may interfere with investigation endpoints.

Treatment and study plan

Soluble Fiber

Other

15g/day during 2 months

Placebo

Other

Maltodextrin 15g/day during 2 months

Primary outcomes

  1. Change from baseline HI titers at 2 months

    Time frame: at Month 1 (before influenza vaccination), at Month 2 (one month after influenza vaccination)

    hemagglutination inhibition (HI) antibody titers after vaccination

Secondary outcomes

  1. Intestinal Microbiota

    Time frame: at month 0, At month 1, at month 2

    The microbiota is characterized using the Shotgun bacterial DNA analysis method on feces samples

  2. Inflammatory biomarker

    Time frame: at month 0, at month 1, at month 2

    Interleukins

  3. Cytokin biomarker

    Time frame: at month 0, at month 1, at month 2

    Tumour Necrosis Factor alpha cytokin

  4. Incidence of Treatment on hematologic blood parameters

    Time frame: at month 0, at month 1, at month 2

    Complete blood count

  5. Incidence of Treatment on biochemical blood parameters

    Time frame: at month 0, at month 1, at month 2

    Transaminases

Sponsors and collaborators

Lead sponsor

CEN Biotech

Industry

Collaborators

  • Roquette Freres

Registry information

Official study title

Evaluation of the Effect of a Soluble Fiber Consumption on the Immune Response Post-influenza Vaccination in Healthy Subjects Aged 50 to 70 Years

Acronym: NUTIVAC

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Apr 6, 2022
Registry last updated
Dec 26, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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