Actively Recruiting
Biological Collection for Studying Vaccine-induced Immune Responses
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2020-12-14
1200
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
A
Assistance Publique - Hôpitaux de Paris
Lead Sponsor
I
Institut National de la Santé Et de la Recherche Médicale, France
Collaborating Sponsor
AI-Summary
What this Trial Is About
Vaccination plays a crucial role in reducing illness and death from infectious diseases worldwide. Researchers are studying how the immune system responds to various vaccines, including influenza, pneumococcal, MMR, and yellow fever vaccines, especially in different groups such as healthy individuals, people living with HIV, COPD patients, and those with primary immune deficiencies. This observational study aims to better understand the immune responses triggered by these vaccines using modern immune analysis techniques. The study collects blood samples from participants receiving vaccines as part of their routine care. It uses advanced methods like transcriptional analysis to examine the innate immune response 24 hours after vaccination, as well as measuring B and T cell responses and specific antibody production at various times up to one month post-vaccination. The goal is to identify immunological markers that relate to vaccine protection in diverse populations. Participants will provide samples before vaccination and at several points afterward, including days 7, 14, and one month. Researchers will perform detailed laboratory tests to analyze immune cells and antibodies. The study carefully observes changes in immune responses over time to improve knowledge about how vaccines work in different people. The total participation time varies depending on vaccination schedules, with ongoing monitoring of immune markers to support vaccine research.
CONDITIONS
Brief Title
Post-Vaccination Biological Collection
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 218 years old
- Able to give informed consent
- Scheduled to receive vaccination as part of routine care
You will not qualify if you...
- Under legal guardianship or protective supervision
- Pregnant or breastfeeding women
- Not affiliated with a health insurance scheme
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 month
Participants provide biological samples to study immune responses induced by vaccination.
4 visits at Day 0, Day 7, Day 14, and Month 1 after vaccination
Trial Site Locations
Total: 1 location
1
Pr Gallien
Créteil, France, 94000
Actively Recruiting
Research Team
S
Sébastien Gallien, PHD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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