Actively Recruiting

Age: 18Years +
All Genders
ID03875703

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 218 years old
  • Able to give informed consent
  • Scheduled to receive vaccination as part of routine care
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Sample Collection

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

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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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