Probiotic, Prebiotic and Synbiotic Effect on Immunity

Double-blind, Placebo Controlled Randomized Parallel Study to Determine the Effects of Pre-pro and Synbiotic Administration on the Immune Response to Influenza Vaccination and Faecal Microbiota in Healthy Adults

The aim of the study is to investigate the effect of dietary supplements such as probiotic, prebiotic and synbiotic on the immune response to influenza vaccination and faecal microbiota in adult healthy volunteers.

Study Overview

• Status: Unknown
• Conditions: Dietary Intervention
• Intervention / Treatment: Dietary supplement: probiotic; Dietary supplement: prebiotic; Dietary supplement: Synbiotic; Dietary supplement: Placebo

Detailed Description

Within recent times, influenza has become a major respiratory infection worldwide. The preventative vaccination reduces the severity of infection but ageing reduced its efficacy and it is only effective in 17-53% in elderly individuals. Thus, nutritionists and medical researchers are looking for opportunities to improve the immune response to influenza vaccine. Functional foods, such as probiotics, prebiotics and synbiotics, apart from other health benefits, may contribute towards immune protection.

Probiotics are beneficial bacteria, which are regarded as safe and serve health benefits to the host, while prebiotics are carbohydrates which by escaping digestion in the upper gastrointestinal tract may reach the colon and there serve as food for beneficial bacteria in the colon. When prebiotic used in combination with probiotic bacteria, it is called synbiotic, and it may improve survival and implantation of probiotic in the gut.

The human study will examine the immune response to vaccination and changes in faecal microbiota during administration of probiotic, prebiotic and synbiotic supplements. The study will be conducted between vaccinations seasons in 2010-2011 and recruit 100 healthy subjects aged 40-65years old. Participant will be given one of four different treatments over a 7 week period following 3 weeks of wash-out period. Treatments given include: a probiotic, a prebiotic, a synbiotic and a placebo. In the 3rd week of product consumption the participant will be given a flu jab. Specific antibody titre against the 3 viral strains composing the vaccine and total immunoglobulin concentration in the serum will be monitored during 2 and 4 weeks after vaccination. Faecal samples and saliva will be collected and analysed for changes in faecal microbial populations.

• Study Type: Interventional
• Enrollment (Anticipated): 100
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United Kingdom
  • Berkshire
    • Reading, Berkshire, United Kingdom, RG66AP
      • University of Reading, Food and Nutritional Sciences Department

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 45 years to 65 years (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Signed consent form
• Age 40-65 years
• Body mass index 18.5-30 inclusive
• Good general health as determined by medical questionnaires
• Not vaccinated with the current seasonal influenza (2009) or swine flu vaccine

Exclusion Criteria:

• Evidence of physical or mental disease or planned major surgery, which might limit participation in or completion of the study
• History of drug misuse, including alcohol
• Allergy to the vaccine
• Asplenia and other acquired or congenital immunodeficiency
• Severe allergy such as asthma, hay-fever, dermatitis or being treated on these
• History of severe abnormal drug reaction
• Any autoimmune disease
• Diabetic (type 1 or type2)
• Food allergy manifested by gastrointestinal, skin, respiratory , neurological, anaphylaxis symptoms
• Lactose intolerance showed by clinical symptoms such as nausea, cramping, bloating, diarrhea and flatulence after consuming lactose containing dairy products (milk, yoghurt, butter, cheese, ice-cream, sour cream) or lactose non-dairy products ( whey, milk solids, modified milk ingredients)
• Participation in experimental drug trial within four weeks prior to study
• Participation in prebiotics or laxative trial within the previous three months
• Use of antibiotics within the previous six months
• Chronic constipation, diarrhoea or other chronic gastro-intestinal complaint
• Intake of other prebiotics or probiotics, drugs active on gastrointestinal motility, or a laxative of any class for four weeks prior to study
• Use of prescribed medication
• Regular use of aspirin or other anti-inflammatory drugs

Study Plan

How is the study designed?

Design Details

• Primary Purpose: TREATMENT
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: DOUBLE

Number of Arms

4

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
EXPERIMENTAL: Probiotic group; Group of 25 volunteers consuming probiotic product once a day for 7 weeks	Dietary supplement: probiotic; Bifidobacterium lactis HN019 10^9 CFU/day 1 sachet once a day for 7 weeks; Other Names: HOWARU Bifidobacterium lactis
EXPERIMENTAL: Prebiotic group; Group of 25 volunteers consuming prebiotic product once a day for 7 weeks	Dietary supplement: prebiotic; Galactooligosaccharide 5.5 g/day 1 sachet once a day for 7 weeks; Other Names: Bimuno
EXPERIMENTAL: Synbiotic group; Group of 25 volunteers consuming synbiotic product once a day for 7 weeks.	Dietary supplement: Synbiotic; (Bifidobacterium lactis 10^9 CFU + Galactooligosaccharide 5.5g) / day - 1 sachet once a day for 7 weeks
PLACEBO_COMPARATOR: Placebo group; Group of 25 volunteers consuming placebo product once a day for 7 weeks	Dietary supplement: Placebo; Maltodextrin 5.5g/day - 1 sachet once a day for 7 weeks

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
The primary outcome would be a higher change in antibody levels in response to influenza vaccination compared to placebo group.	2 and 4 weeks after vaccination

Secondary Outcome Measures

Outcome Measure	Time Frame
The secondary outcome would be a change in faecal microbiota groups and a change in their metabolic activities.	at 0, 7 and 10 weeks on pro-, pre,synbiotic treatment

Collaborators and Investigators

• Sponsor: University of Reading
• Investigators: Principal Investigator: Maria Magdalena Baran, MSc; Principal Investigator: Sofia Kolida, PhD

Study record dates

Study Major Dates

• Study Start: May 1, 2010
• Primary Completion (ANTICIPATED): January 1, 2011
• Study Completion (ANTICIPATED): June 1, 2011

Study Registration Dates

• First Submitted: February 18, 2010
• First Submitted That Met QC Criteria: March 9, 2010
• First Posted (ESTIMATE): March 10, 2010

Study Record Updates

• Last Update Posted (ESTIMATE): March 10, 2010
• Last Update Submitted That Met QC Criteria: March 9, 2010
• Last Verified: February 1, 2010

More Information

Terms related to this study

• Other Study ID Numbers: F3168407