Immunopathology of Loeys-Dietz Syndrome (I-LoDiS)

Civil Hospices of Lyon

Status

Completed

Conditions

Loeys-Dietz Syndrome

Treatments

Biological: blood samples

Study type

Interventional

Funder types

Other

Identifiers

NCT05472519

69HCL22_0016

Details and patient eligibility

About

Loeys-Dietz syndrome (LDS) is a rare vascular genetic disorder (estimated prevalence 1/25,000-1/100,000) due primarily to mutations in the Transforming growth factor beta (TGF-β) cytokine receptor 1 and 2 genes. In addition to a common vascular phenotype with Marfan syndrome (dilatation of the ascending aorta, arachnodactyly, lens dislocation), patients present specific malformations (bifid uvula, hypertelorism, tortuous arteries) and immuno-allergic manifestations (asthma, eczema, food allergy, eosinophilic esophagitis, chronic inflammatory bowel disease).

Pathophysiologically, LDS appears to be associated with hyperactivation of the intracellular TGF-β signaling pathway in a manner similar to Marfan syndrome, as evidenced by increased intracellular phosphorylated Smad2/3 (pSmad2/3) in lymphocytes. The immuno-allergic complications appear paradoxical because of the major immunosuppressive role of this cytokine on lymphoid and myeloid immune lineages.

The biological description of immunological abnormalities associated with LDS is based on a single 2013 study that found increased regulatory T (Treg) and Th2 lymphocyte polarizations, as well as increased circulating eosinophil and total IgE levels.

In order to better understand the underlying mechanisms, the investigators propose to perform a descriptive clinical-biological study to identify and study the immune subpopulations most impacted by the causative mutations of LDS.

Enrollment

60 patients

Sex

All

Ages

5 to 86 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

For patients with Loeys-Dietz syndrome:

Patients aged ≥ 5 years with Loeys-Dietz syndrome with a diagnosis confirmed by the presence of a TGF-βR 1 or R2 mutation known to be pathogenic to patients.
Free, informed and signed consent from the patient or both parents or legal guardians for minor patients.
Patient affiliated to a social security system or similar.

For healthy volunteers:

Subjects aged ≥ 5 years.
Free, informed and signed consent of the witness, or if applicable of both parents or legal representatives for minors.
Patient affiliated to a social security system or similar.

Exclusion criteria

For patients with Loeys-Dietz syndrome:

Patient with an evolving or recently healed (< 3 months) cancer that could alter the immunologic profile.
Patient with an evolving or recently healed (< 3 months) infection that could alter the immunologic profile.
Patient with a weight of less than 20 kg.
Pregnant woman.
Patient participating in another research study with an exclusion period exclusion period still in progress.

For healthy volunteers:

Subject with an active or recently cured (< 3 months) cancer that could alter the immunologic profile.
Subject with an active or recently healed (< 3 months) infection that could alter the immunological profile.
Patient with a weight of less than 20 kg.
Pregnant woman.
Subject participating in another research study with an exclusion period exclusion period still in progress.
Persons under court protection.