RecruitingNot ApplicableNCT07111793

Identification of Clinical, Genetic and Immunological Factors Involved in the Development of Severe Bacterial Infections in Pediatrics

IBSoFACTo : Identification of Clinical, Genetic and Immunological Factors Involved in the Development of Severe Bacterial Infections in Pediatrics


Sponsor

Nantes University Hospital

Enrollment

1,401 participants

Start Date

Mar 18, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Severe bacterial infections (SBI) are responsible for significant morbidity and mortality in the paediatric population. There is considerable individual variability in children's susceptibility to developing SBIs. This variability is multifactorial, and the mechanisms at work are not yet fully understood. The investigators of this study therefore propose to study a population of children who had particularly severe bacterial infections requiring hospitalization in a pediatric intensive care unit in France between 2015 and 2018. This study is part of a global approach to understanding the mechanisms favoring the occurrence of IBS in pediatrics. The study will initially focus on analyzing the clinical phenotype of these children in terms of the type of infection presented, as well as immunologically with an immune workup of all these patients. The investigators also plan to contact each family individually to identify other episodes of personal or family IBS or other elements suggestive of immune deficiency (opportunistic infections, autoimmune manifestations, severe atopy). The investigators will also assess the persistent sequelae since their infectious episode, and their quality of life following this IBS. In parallel, the genetic analysis of these patients and their parents will be carried out using whole-exome sequencing. The investigators will compare the results with those obtained in 2 IBS-free control populations (N=70 and N=116). The goal is to identify genetic variants that favor the occurrence of IBS in general, and some that are specific to certain bacteria or clinical presentations.


Eligibility

Inclusion Criteria8

  • For patients:
  • Patient included in the DIABACT IV study between 2015 and 2018, following hospitalization in a pediatric intensive care unit in France for a severe bacterial infection.
  • Patient affiliated to a social security system
  • Patient alive at the time of inclusion.
  • Written consent from legal representatives for participation in research. If one of the legal representatives is unable to complete/sign the written consent, it will be sought orally by telephone and recorded in the patient's file. If the patient is over 18, written consent will be obtained. If the patient is a minor, consent will be sought with communication adapted to his/her level of understanding and age.
  • For parents:
  • Patient's biological parents
  • Written consent

Exclusion Criteria2

  • Persons under court protection
  • Refusal to participate in research

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Interventions

OTHERExtended phenotyping

Extended phenotyping (analysis performed at Nantes University Hospital, MANDATORY DELIVERY WITHIN 24 HOURS) = 1 EDTA 3 mL tube for patients included in Nantes.

OTHERBlood sample for WES

Blood sample for WES : 1 x 3 mL EDTA tube (if not included in DIABACT IV biocollection)

OTHERBlood sample for PBMC freezing

Blood sample for PBMC freezing integrated into the biocollection: 1 EDTA tube = 3 mL

OTHERPOPC score evaluation

Assessment of POPC score (Pediatric Overall Performance Category)

OTHERQuestionnaire completion

Questionnaires completed by parents or children: * SDQ * PedSQL4.0


Locations(6)

Nantes University Hospital

Nantes, Loire Atlantique, France

CHU de Brest

Brest, France

Hospices Civils de Lyon

Lyon, France

Hôpital Armand Trousseau

Paris, France

Hôpital Necker enfants malades

Paris, France

CHU de Saint-Étienne

Saint-Etienne, France

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NCT07111793