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OpenTrials
Completed

NCT Number: NCT01652066

Effect of a Mixture of Probiotics on the Antigen Specific Antibody Response in a Influenza Vaccination Model of Healthy Adults

the aim of the study is to get evidence for an enhancement of immune status in subjects after probiotics mixture consumption ( lactobacillus gasseri PA 16/8, Bifidobacterrium longum SP 07/3, Bifidobacterium bifidum MF 20/5) based on influenza vaccination model - compared to placebo.

Completed

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Biofortis

Nantes, 44200, France

About this study

probiotics are "live microorganisms which when administered in adequate amounts confer a health benefit on the host" . many health effects are associated with probiotics , but various degrees of evidence support the benefits associated to probiotics consumption . Impact on defences and the immune system has been shown with several strains and this may result in improved protection against some infections or improvment of vaccine efficacy .

In its scientific requirments for health claims related to immune function, EFSA indicates that it is generally accepted that higher vaccination responses are beneficial.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • healthy male and female adult
  • between 18 and 60 years old non menopausal female( with effective contraception)
  • female non pregnant- not wishing to be pregnat during the study capable to respect the protocol
  • affialted to the social security system aggreeing to be registered in the national fileof volunteers

Exclusion criteria

  • food allergy( component of the experimental product- vaccines)
  • manifestation of allergy
  • vaccinated against flu during the 2 previous winters
  • Food allergy, allergy to one of the component of the experimental products or allergy to one of the component of the flu vaccine;
  • Subject displaying manifestation of allergy or being treated for these;
  • Subject vaccinated against flu during the 2 previous winter (winter 2009-2010 and winter 2010-2011);
  • Subject who had symptoms evocating flu during the previous winter (winter 2010-2011);
  • Subject immunodepressed;
  • Subject with immunomodulatory treatment;
  • Subject who received a treatment resulting in systemic immunossuppression or local immunosuppression at pulmonary level, for at least 1 week during the last 3 months before inclusion (V1);
  • Subject with auto-immune disease;
  • Subject with inflammatory and chronic diseases;
  • Subject with on-going antibiotics treatment at the time of the inclusion;
  • Subject not agree to stop his/her usual probiotics supplementation during the study;
  • Use of medication which could interfere with the study in the investigator's opinion (antibiotics, etc…);
  • Any health condition for which the influenza vaccine is not recommended;
  • Subject having received any other vaccine within one month prior to enrolment or intent to receive any other vaccination during the study period.

Treatment and study plan

Mixture of probiotics

Dietary Supplement

effect of the consumption a mixture of probiotics ( dietary supplement tablet - dosage at least 10x7 cfu/g) during 7 weeks , once a day , healthy volonteers ) on the antigen specific antibody respense

Mixture of probitiocs

Dietary Supplement

effect of the consumption a mixture of probiotics ( dietary supplement tablet - dosage at least 10x7 cfu/g) during 7 weeks , once a day , healthy volonteers ) on the antigen specific antibody respense

Primary outcomes

  1. geographic mean of the increase of antibody titreq against at least one flu strain among the 3 forming the flu vaccine ( H1N1, H3, N and B ) within 3 weeks after flu vaccination

    Time frame: inclusion-W 4-W 7

Secondary outcomes

  1. seroprotection of the population of volunteers geometric mean of the increase of antibody titres seroprotection in the subset population non sero-protected at V1

    Time frame: inclusion- W4- W7

Sponsors and collaborators

Lead sponsor

Merck Medication Familiale

Industry

Collaborators

  • BioFortis

Registry information

Official study title

Effect of a Mixture of Probiotics ( Lactobacillus Gasseri PA16/8,Bifidobacterium Longum SP07/3, Bifidobacterium Bifidum MF 20/5) on the Antigen Specific Antibody Response in a Influenza Vaccination Model of Healthy Adult

Acronym: PROBIMMUNE

Important dates

Study start
2011
Primary completion
2011
Study completion
2011
First posted
Jul 27, 2012
Registry last updated
Jul 27, 2012

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.