ConditionsAutoimmune Lymphoproliferative SyndromeAutoimmune CytopeniaAutoimmune DiseasesAutoimmune AnemiaAutoimmune ThrombocytopeniaAutoimmune HepatitisAutoimmune DiabetesAutoimmune Rheumatologic DiseaseSystemic Lupus ErythematosusJuvenile Idiopathic ArthritisHemophagocytic LymphohistiocytosesEBV LymphoproliferationRAS-Associated Autoimmune Leucoproliferative DiseasePrimary ImmunodeficiencyAPECEDIPEXBENTAEnteropathy, AutoimmuneCombined ImmunodeficiencyIBD
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age1-18
SponsorInstitut National de la Santé Et de la Recherche Médicale, France
About this trial
The main objective of this study is to generate diagnosis and therapeutic-decision tools through the identification of molecular causes of PIDs with autoimmunity/inflammation and the variability in disease outcome at the transcriptional level using a combination of omics signatures (transcriptomics, epigenomics, proteomics, metagenomics, metabolomics and lipidomics).
Eligibility criteria
Qualifiers
Individuals aged<18 y/o.
Individuals > 6 kg
Individuals not affected by an immune-related disease or not affected by cancer
Individuals whose parents have signed an enlightened consent.
Disqualifiers
Intake of antibiotics within 2 weeks prior inclusion
Absence of parent's or child consent form
Cytotoxic cancer treatments
antiviral treatments (HIV, hepatitis …)
Trial design
Treatments tested in this trial
- Collection of samples
Treatment groups
500 Participants
are divided into 3 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov