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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
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
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| People with an indication for primary immunization against yellow fever and typhoid | Other | People with an indication for primary immunization against yellow fever and typhoid and whose vaccination schedule includes two appointments 7 days apart |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| blood samples collection | Biological | blood samples collected at D0 ,W1, W5, M3 and M6 |
|
| Measure | Description | Time Frame |
|---|---|---|
| Immunological profile of PBMCs, before and after yellow fever vaccination | Cytokine production assays (e.g. TNFa, IL6, IL1b) | 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| Description of the response to TyphimVi® vaccine | ELISA-based quantification of Anti-Vi antibody level >30 U/mL at week 5, and/or fold increase ≥2 compared with pre-vaccination IgG titer. | 6 months |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Jessica Quintin, Dr | Contact | 144389454 | +33 | jessica.quintin@pasteur.fr |
| Sandrine Fernandes Pellerin | Contact | 145688179 | +33 | sandrine.fernandes-pellerin@pasteur.fr |
| Name | Affiliation | Role |
|---|---|---|
| Fabien Taieb, Dr | Institut Pasteur | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Centre Médical de l'Institut Pasteur | Recruiting | Paris | 75015 | France |
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| ID | Term |
|---|---|
| D007239 | Infections |
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