Description of the Immune Response to Yellow Fever Vaccination
NCT ID: NCT06718127
Last Updated: 2025-06-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
38 participants
INTERVENTIONAL
2024-09-30
2027-04-30
Brief Summary
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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
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Detailed Description
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For example, research has shown that the live attenuated BCG vaccine induce non-specific trained immunity, enabling innate immune cells to remember their first encounter and improve their immune status during a second confrontation with similar or different agents.
Other currently available live vaccines, such as BCG , could also "train" innate immune cells.
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
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Study Design
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NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
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People with an indication for primary immunization against yellow fever and typhoid
People with an indication for primary immunization against yellow fever and typhoid and whose vaccination schedule includes two appointments 7 days apart
blood samples collection
blood samples collected at D0 ,W1, W5, M3 and M6
Interventions
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blood samples collection
blood samples collected at D0 ,W1, W5, M3 and M6
Eligibility Criteria
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Inclusion Criteria
* Referred for immunisation against yellow fever and typhoid
* Any person with indication for the following vaccinations :
* Yellow fever
* Typhoïd
* Whose vaccination schedule includes two appointments 7 days apart
* Whose state of health is compatible with a single 51 ml blood sample collection
* Have consented to participate in the Ivory2 study
* Benefiting from a Social Security plan or equivalent
Exclusion Criteria
* Any person who has been vaccinated against yellow fever and/or typhoid.
* Anyone who has lived in an endemic area (≥ 1 year) and/or has a history of Typhoid.
* Anyone who is unable to attend the visit 1-month after the typhoid vaccine injection.
* Women claiming to be pregnant or breast-feeding
* Anyone unable to give informed consent for participation
18 Years
65 Years
ALL
Yes
Sponsors
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Institut Pasteur
INDUSTRY
Responsible Party
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Principal Investigators
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Fabien Taieb, Dr
Role: PRINCIPAL_INVESTIGATOR
Institut Pasteur
Locations
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Centre Médical de l'Institut Pasteur
Paris, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2023-149
Identifier Type: -
Identifier Source: org_study_id
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