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OpenTrials
Completed

NCT Number: NCT02238548

Effect of Raw Milk on the Immune Response Upon Cholera Vaccination

Rationale: Infections are an important worldwide cause of death, both in elderly and young children. Therefore, support of immunity could help to reduce the incidence of infections. To screen the potential of specific foods or food ingredients to support immunity, oral vaccination can serve as a model. In this study, oral cholera vaccination will be applied in human adult volunteers, and used as a model to study the support of the immune response by raw milk.

Objective: To investigate whether raw milk is able to enhance the immune response as induced by oral cholera vaccination.

Study design: The study is designed as a single-blind randomized controlled trial of 4 weeks.

Study population: Healthy subjects of 18-50 years of age.

Intervention: Raw milk, obtained from farms that comply to the high quality requirements for production of raw milk, and that has been screened according to the safety criteria for raw milk.

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Key information

Conditions

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

NIZO food research

Ede, 6718 ZB, Netherlands

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Age 18-50 yr
  • Signed informed consent
  • Availability of internet connection
  • Male or female
  • Willing to stop blood donation at the blood bank during the study period

Exclusion criteria

  • Currently participating in another clinical trial
  • Previous Cholera, Salmonella, or E. coli vaccination
  • Tonsillectomy
  • Acute gastroenteritis in the past 2 months
  • Use of antibiotics in the past 2 months
  • Hypersensitivity to the vaccine, to formaldehyde or to any of the excipients (sodium salts)
  • Pregnancy or lactating (pregnancy test will be performed on the vaccination days)
  • Not willing to drink raw milk
  • Allergic to milk or lactose-intolerant
  • Disease of GI tract, liver, gall bladder, kidneys, thyroid gland
  • Immune-compromised
  • Use of immunosuppressive drugs
  • Drug abuse, and not willing/able to stop this during the study
  • Excessive alcohol usage (men: >4 consumptions/day or >20 consumptions/week; women: >3 consumptions/day or >15 consumptions/week)

Treatment and study plan

cholera vaccination

Biological

Oral cholera vaccination on day 0 and day 14

Other names: Dukoral

raw milk

Other

Primary outcomes

  1. Change in cholera toxin-specific IgA and IgG antibody level in nasal wash as a marker of the vaccination response

    Time frame: baseline and day 18

Secondary outcomes

  1. Change in the cholera toxin-specific IgA and IgG antibody level in serum as a marker of the vaccination response

    Time frame: baseline and day 18

  2. Change in the cholera toxin-specific IgA antibody level in feces as a marker of the vaccination response

    Time frame: baseline and day 28

  3. Change in the cholera toxin-specific IgA and IgG antibody level in saliva as a marker of the vaccination response

    Time frame: baseline and day 18

  4. Change in the expression of tissue homing markers on IgA and IgG antibody-secreting B cells in peripheral blood as markers of the route of modulation of the vaccination response

    Time frame: baseline and day 18

  5. Cholera toxin-specific T cell proliferation as marker of modulation of the vaccination response

    Time frame: baseline and day 28

Sponsors and collaborators

Lead sponsor

NIZO Food Research

Other

Collaborators

  • FrieslandCampina

Registry information

Acronym: MOSAIC

Important dates

Study start
2014
Primary completion
2014
Study completion
2016
First posted
Sep 12, 2014
Registry last updated
Mar 29, 2017

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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