Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
NCT06718127

Description of the Immune Response to Yellow Fever Vaccination

Led by Institut Pasteur · Updated on 2025-06-29

38

Participants Needed

1

Research Sites

134 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Vaccine protection depends on a specific adaptive immune memory. However, a little-explored aspect of certain live vaccines may provide beneficial, non-specific protection against infections or pathogens other than the one from which the vaccine is derived. This is the concept of innate immune memory or " trained immunity", which differs from adaptive memory in its non-specificity. Innate immune memory is triggered by exposure to immunostimulants, and offers protection against unrelated pathogenic threats for several months or even years. The project aims to carry out an exploratory study to observe, in the context of current practice, the immune response obtained after a subunit and a live attenuated vaccine

CONDITIONS

Official Title

Description of the Immune Response to Yellow Fever Vaccination

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 65
  • Referred for immunisation against yellow fever and typhoid
  • Any person with indication for the following vaccinations : Yellow fever, Typhoid
  • Vaccination schedule includes two appointments 7 days apart
  • Health condition allows for a single 51 ml blood sample collection
  • Have consented to participate in the Ivory2 study
  • Benefiting from a Social Security plan or equivalent
Not Eligible

You will not qualify if you...

  • Contraindication to yellow fever and/or typhoid vaccination
  • Previously vaccinated against yellow fever and/or typhoid
  • Lived in an endemic area for one year or more and/or history of typhoid
  • Unable to attend the visit 1 month after the typhoid vaccine injection
  • Pregnant or breastfeeding women
  • Unable to give informed consent for participation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Centre Médical de l'Institut Pasteur

Paris, France, 75015

Actively Recruiting

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Research Team

J

Jessica Quintin, Dr

CONTACT

S

Sandrine Fernandes Pellerin

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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