Agaricus Bisporus and Influenza Vaccination Response

Sponsor
Maastricht University Medical Center (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06041867
Collaborator
Scelta Mycofriends B.V. (Other), CNC Grondstoffen B.V. (Other)
105
1
2
8.5
12.3

Study Details

Study Description

Brief Summary

There are numerous in vitro and animal studies that suggested that mushrooms beneficially influence the immune system. We have recently shown that a wild isolate of the edible Agaricus bisporus mushroom had a clear effect on parameters reflecting a better function of the immune system, both in vitro and in vivo in animals. The question now is whether this efficacy can also be translated to humans. In humans, measuring the antibody response is the golden standard to evaluate immune function. If Agaricus bisporus powder indeed has beneficial effects on the immune system, people with overweight or obesity and higher age might benefit from consuming Agaricus bisporus powder prior to receiving the influenza vaccination.

Condition or Disease Intervention/Treatment Phase
  • Biological: Influenza vaccine
  • Dietary Supplement: Agaricus bisporus capsules
  • Dietary Supplement: Control capsules
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
105 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Mushboost: Evaluating the Effect of Agaricus Bisporus Powder Intake on the Vaccination Response to an Influenza Vaccine
Anticipated Study Start Date :
Sep 14, 2023
Anticipated Primary Completion Date :
Dec 22, 2023
Anticipated Study Completion Date :
May 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Agaricus bisporus group

Dietary supplement: 10 capsules containing 500 mg Agaricus bisporus powder each

Biological: Influenza vaccine
Single dose of the Influenza vaccine Participants have to wait until they are invited to receive the vaccine by the general practitioner; this study does not interfere with national planning of the vaccine

Dietary Supplement: Agaricus bisporus capsules
Participants have to consume 10 capsules per day containing 500 mg Agaricus bisporus powder each, corresponding to a total Agariicus bisporus powder intake of 5 g daily

Placebo Comparator: Placebo group

Dietary supplement: 10 placebo capsules, capsules that do not contain Agaricus bisporus powder

Biological: Influenza vaccine
Single dose of the Influenza vaccine Participants have to wait until they are invited to receive the vaccine by the general practitioner; this study does not interfere with national planning of the vaccine

Dietary Supplement: Control capsules
Participants have to consume 10 capsules per day containing 500 mg maltodextrin each, corresponding to a total maltodextrin intake of 5 g daily

Outcome Measures

Primary Outcome Measures

  1. Vaccine specific antibody titer [Maximal change form T=0 (change T=0 to T=3 weeks or T=4 weeks)]

    The response to the Influenza vaccine will be measured by quantifying the specific antibody titer

Secondary Outcome Measures

  1. Immune parameters (1) [Day - 1 (start study), T=0 (day before vaccination), T=4 weeks after vaccination (end of study)]

    Cytokine production by PBMCs after stimulation with antiCD3-antiCD28 antiCD28 antibodies using the TruCulture system

  2. Immune parameters (2) [Day - 1 (start study), T=0 (day before vaccination), T=4 weeks after vaccination (end of study)]

    hsCRP

  3. Leukocyte count [Day - 1 (start study), T=0 (day before vaccination), T=4 weeks after vaccination (end of study)]

    Number of leukocytes measured in EDTA plasma

  4. Leukocyte differential count [Day - 1 (start study), T=0 (day before vaccination), T=4 weeks after vaccination (end of study)]

    Number of subgroups of leukocytes measured in EDTA plasma

  5. Fasted metabolism (1) [Day - 1 (start study), T=0 (day before vaccination), T=4 weeks after vaccination (end of study)]

    Serum non-cholesterol sterols and stanols

  6. Fasted metabolism (2) [Day - 1 (start study), T=0 (day before vaccination), T=4 weeks after vaccination (end of study)]

    Serum lipid and lipoprotein profile

  7. Fasted metabolism (3) [Day - 1 (start study), T=0 (day before vaccination), T=4 weeks after vaccination (end of study)]

    Plasma glucose

  8. Fasted metabolism (4) [Day - 1 (start study), T=0 (day before vaccination), T=4 weeks after vaccination (end of study)]

    Ergothioneine

  9. Fasted metabolism (5) [Day - 1 (start study), T=0 (day before vaccination), T=4 weeks after vaccination (end of study)]

    Glutathione

  10. Fasted metabolism (6) [Day - 1 (start study), T=0 (day before vaccination), T=4 weeks after vaccination (end of study)]

    Malondialdehyde

  11. Anthropometry (1) [Day - 1 (start study), T=0 (day before vaccination), weekly in the month after vaccination (T1-T4)]

    Body weight

  12. Anthropometry (2) [Day -1 (start study)]

    Height

  13. Anthropometry (3) [Day - 1 (start study), T=0 (day before vaccination), weekly in the month after vaccination (T1-T4)]

    Waist circumference

  14. Anthropometry (4) [Day - 1 (start study), T=0 (day before vaccination), weekly in the month after vaccination (T1-T4)]

    Hip circumference

  15. Anthropometry (5) [Day - 1 (start study), T=0 (day before vaccination), weekly in the month after vaccination (T1-T4)]

    Waist-to-hip ratio

  16. Diet [Day - 1 (start study), T=4 weeks after vaccination (end of study)]

    Food frequency questionnaire is used to determine if the participants maintain their habitual diet and to determine if the participants do not consume mushrooms outside the intervention

  17. Quality of life questionnaire [Day - 1 (start study), T=4 weeks after vaccination (end of study)]

    Quality of life questionnaire is used to determine the participants overall wellbeing and quality of life

  18. Diary outcomes (1) [Day - 1 (start study), T=4 weeks after vaccination (end of study)]

    Adverse events as assessed by the diary

  19. Diary outcomes (2) [Day - 1 (start study), T=4 weeks after vaccination (end of study)]

    Medication intake as assessed by the diary

Eligibility Criteria

Criteria

Ages Eligible for Study:
59 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Aged 60 years or older during influenza season 2023/2024 (in line with RIVM guidelines)

  • BMI between 20 and 35 kg/m2

  • Willing to abstain from mushrooms other than the capsules containing a mushroom powder as provided by us during the study period.

  • Willing to keep the intake of fish oil, Zinc, Selenium and (vitamin) supplements constant

  • Willing to abstain from products / supplements enriched with Vitamin D

  • Willing to abstain from products / supplements enriched with plant sterols or stanols

  • Willing to abstain from products / supplements enriched with (β)glucans or fungi.

  • Willing to abstain from products / supplements that are mentioned to "boost your immune system"

  • Willing to abstain from (products enriched in) pre/pro-biotics

  • Willing to abstain from products/supplements enriched with ergothioneine

Exclusion Criteria:
  • Already received influenza vaccination in 2023

  • Allergy to mushrooms

  • Known allergic reaction to an active component or other components of the vaccine (e.g. Chicken Eggs)

  • Having donated blood within one month prior to the start of the study, or planning to donate blood during the study

  • Excessive alcohol use (>20 consumptions per week)

  • Regular use of soft and/or hard drugs

  • Using medication for diseases known to affect inflammation/immunity (e.g. inhaled corticosteroids and prednisone)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Maastricht University Medical Center Maastricht Limburg Netherlands 6229 ER

Sponsors and Collaborators

  • Maastricht University Medical Center
  • Scelta Mycofriends B.V.
  • CNC Grondstoffen B.V.

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Maastricht University Medical Center
ClinicalTrials.gov Identifier:
NCT06041867
Other Study ID Numbers:
  • METC 23-026
First Posted:
Sep 18, 2023
Last Update Posted:
Sep 18, 2023
Last Verified:
Jul 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Maastricht University Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 18, 2023