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Description of the Immune Response to Yellow Fever Vaccination (IVORY2)

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Pasteur Institute

Status

Enrolling

Conditions

Immunization
Infections

Treatments

Biological: blood samples collection

Study type

Interventional

Funder types

Industry

Identifiers

NCT06718127
2023-149

Details and patient eligibility

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

Full description

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.

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

Enrollment

38 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age between 18 and 65
  • 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

  • Anyone with a contraindication to yellow fever and/or typhoid vaccination.
  • 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

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

38 participants in 1 patient group

People with an indication for primary immunization against yellow fever and typhoid
Other group
Description:
People with an indication for primary immunization against yellow fever and typhoid and whose vaccination schedule includes two appointments 7 days apart
Treatment:
Biological: blood samples collection

Trial contacts and locations

1

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Central trial contact

Sandrine Fernandes Pellerin; Jessica Quintin, Dr

Data sourced from clinicaltrials.gov

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