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Immunopathology of Loeys-Dietz Syndrome

Immunopathology of Loeys-Dietz Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05472519
Acronym
I-LoDiS
Enrollment
60
Registered
2022-07-25
Start date
2022-10-17
Completion date
2023-06-07
Last updated
2023-06-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Loeys-Dietz Syndrome

Keywords

Loeys-Dietz Syndrome, immunology, T-Lymphocytes

Brief summary

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.

Interventions

BIOLOGICALblood samples

Only one visit for each participant: A large majority of visits will be part of patients' usual care. * Medical examination : weight, gender, blood pressure, medical history * Blood samples : 1 EDTA tube (3 mL) for CBC, 3 heparin tubes (3 × 7 mL) for frozen PBMC, 1 EDTA tube (3 mL) for frozen plasma

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to 86 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Percentage of circulating TFH lymphocyte subpopulation.Day 1Measured from the Blood samples of each patients / volunteers.

Secondary

MeasureTime frameDescription
Intracellular pSmad2/3 labeling level of circulating TFH lymphocytes.Day 1Measured from the Blood samples of each patients / volunteers.
Identification of Immuno-allergic pathologiesDay 1Identification of Immuno-allergic, serious infectious pathologies (diagnostic criteria, severity criteria, treatment, current activity) in LDS patients.
Identification of serious infectious pathologiesDay 1Identification of serious infectious pathologies (diagnostic criteria, severity criteria, treatment, current activity) in LDS patients.
Identification of Vascular complicationsDay 1Identification of Vascular, morpho-skeletal complications (diagnostic criteria, severity criteria, treatment, current activity) current course) in patients with LDS.
Identification morpho-skeletal complicationsDay 1Identification of morpho-skeletal complications (diagnostic criteria, severity criteria, treatment, current activity) current course) in patients with LDS.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026