Detail Article

Informations générales (source: ClinicalTrials.gov)

Numéro NCT

NCT03925272 Statut inconnu

Titre

Constitution d'Une Cohorte Prospective de Sujets Sains et Malades et d'Une Collection de Ressources Biologiques associées Pour l'étude du système Immunitaire et de Ses déterminants Génétiques et Environnementaux"

Type

Interventional

Pathologie

Phase

N/A

Promoteur

Institut Pasteur (Voir sur ClinicalTrials)

Date de début

février 2011

Date de fin

décembre 2023

Dernière mise à jour

04 juillet 2026

Résumé

CoSImmGEn is a protocol set up to respond to the current lack of healthy and sick population cohorts. Biological resources from these cohorts allow researchers to study the immune system and its genetic and environmental determinants. Those cohorts and collections are open not only to the Pasteurian community but also to the worldwide scientific community (both public and private) working in the field.

Détail

Voir le détail The CoSImmGEn protocol is dedicated to the study of the immune system in healthy people or people with specific pathologies. It is composed of 6 arms (sub-cohorts): - Arm "main cohort CoSImmGEn": comprised of 5 sub groups (A, B, C, D, M) of healthy adult subjects from various ethno-geographical origins. - Arm "ancillary cohort P" comprised of first-degree relatives (including parents, siblings, or children), whether they are healthy or ill. It will allow, whenever necessary, to remove allelic ambiguities for example for the study of HLA and MHC genes. - Arm "ancillary cohort HS": comprised of subjects suffering from Suppurativa Hidradenitis (or Verneuil's disease.) The investigators will include patients suffering from this disease and their close relatives, in order to understand the genetic, immunological, microbiological and metabolomic bases of this disease. - Arm "ancillary cohort J": comprised of elderly patients (≥ 65 years old) with Alzheimer's disease and with mild, moderate or severe cognitive impairment. It will help understand the role of the gut microbiota in age-related brain deficits. - Arm "ancillary cohort F": comprised of patients with familial adenomatous polyposis and carrying a mutation of the APC (Adenomatous Polyposis Coli) tumor suppressor gene. That arm has been set up to carry out a pilot phase on the role of APC mutations on anti-tumoral immune response. - Arm "ancillary cohort I": comprised of patients with chronic inflammatory diseases such as Ankylosing spondylitis and Crohn's disease. - Arm "ancillary cohort V": comprised of subjects vaccinated against COVID-19. It will help to follow-up the immune response after vaccination against COVID-19 in the general population. Additional arms may be set up through new collaborations in the next few years to study others diseases in which the immune system intervenes, such as: infectious diseases, allergies or cancers. Fermer le détail

Etablissements

Les établissements d'Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
AP-HP - Hôpital Tenon	Michael Atlan, MD	Recrutement non commencé	Contact (sur clinicalTrials)
CDS DE L INSTITUT PASTEUR	Aude Nassif, PhD	En recrutement IDF	Contact (sur clinicalTrials)
Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
Hopital sainte Périne - 75016 - Paris - France	Joelle Brachat, PhD	En recrutement	Contact (sur clinicalTrials)
Institut Pasteur - 75015 - Paris - France	Marie-Noelle Ungeheuer, PhD	En recrutement	Contact (sur clinicalTrials)

Critères

Genre

Tous

Nombre d'inclusion

Critère d'inclusion

- unprotected adults with social security who have attested their consent after
receiving any relevant information about the study

- subjects whose ethno-geographical origin of both parents is known

- subjects for whom data on principal vaccinations (diphtheria, tetanus,
poliomyelitis, hepatitis B, possibly tuberculosis) are documented

- subjects who consented to carry out serological tests HIV, HCV, HBV

Exclusion Criteria:

Critère de non inclusion

- Any conditions that would not allow participation in the present study, on the
opinion of the investigator (documenting), ie any acute or chronic pathology that
may interfere with the immune system, such as progressive or chronic pathology
severe or uncontrolled by current treatments or a pathology requiring the
administration of immune impact drugs: long-term anti-inflammatory,
immunosuppressive, etc

- Pregnant or lactating women

- For the realization of skin biopsies: allergy to local anesthetics, cardiac
valvulopathy

- For the realization of Tubertest: Subject presenting a contraindication to
tuberculin

NCT03925272 - Constitution d'Une Cohorte Prospective de Sujets Sains et Malades et d'Une Collection de Ressources Biologiques associées Pour l'étude du système Immunitaire et de Ses déterminants Génétiques et Environnementaux"

Informations générales
Etablissements
Critères
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