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Clinical Trials in France / NCT06824779
Active, not recruiting Phase 4

Impact of FLU Vaccination on Nasal Resident Memory Immune Responses and Peripheral Respiratory-tropic Memory Immune Responses

NCT06824779 · tracked via the Priya Life Science France tracker
Phase
Phase 4
Started
2025-12-05
Last updated
2025-12-30

Condition(s) studied

VolunteersFlu Vaccine

Investigational drug(s) / intervention(s)

Flu VaccineBiological samples →

Flu Vaccine: Vaccination against FLU by one of FLU vaccines in the french market

Biological samples: Before and after the FLU vaccination, according the french recommendations, the following samples will be collected : Nasal fluid sampling Saliva sampling Blood samples Nasal cell sampling

Study summary

Mucosal sites, such as respiratory mucosa, are the primary entry points entry points for pathogens. However, clinical evaluation of vaccines against respiratory respiratory pathogens is currently based primarily on analysis of systemic, i.e. peripheral antibody and cellular responses. These measurements give little indication of the immune responses in respiratory tissues tissues, even though the latter are essential for protection against infection. Protective immune responses in mucous membranes, including respiratory including respiratory tissues, rely on secretory IgA to neutralize pathogens neutralization of pathogens on the mucosal surface, as well as the development of the development of cellular responses, notably those from T (Trm) and B (Brm) lymphocytes. Preclinical studies and a few human studies have demonstrated that Trm are a crucial element mucosal protection against viral and bacterial infections. In fact it has been shown that resident memory lymphocytes, including Trm, are able to able to reside in nasal, pulmonary, intestinal, genital and skin mucosa and skin after infection.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Affiliated to the Social Security System * Signed informed consent form * Having decided to be vaccinated against the flu Exclusion Criteria: * History of recurrent nosebleeds or systemic hemorrhages * Previous injury or surgery which modified nasal cavity (e.g. deviated nasal septum) * Individuals receiving anticoagulant therapy * Individuals who experienced a severe respiratory infection leading to hospitalization in the last 6 months * Individuals who received an antibiotic therapy for respiratory infection or any other infection in the last 6 months * Immunocompromised individuals, or individuals taking immunosuppressed therapy or having a pathology (chronic infection, auto-immune disease) which could impact on immunity based on investigator's opinion * Allergy to any component of the vaccines used in the study * Unstable chronic pathology * People deprived of liberty or hospitalized without any consent * People under guardianship (authorship or curators) * Individuals who received a vaccine (any vaccine) in the last 30 days * Pregnant or breast-feeding people * Individuals experiencing respiratory infection symptoms. Inclusion will be postponed up to 7 days after the symptom resolution * People with no command of the French language

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
CHU de Saint-Etienne Saint-Etienne France

More Centre Hospitalier Universitaire de Saint Etienne trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06824779 on ClinicalTrials.gov ↗ ← All trials in France