defective antibody production of unknown cause primary immunodeficiency
Conditions
Interventions
None listed
Sponsors
Universitair Medisch Centrum Utrecht
Eligibility
Age
2 Years to 99 Years
Inclusion criteria
Inclusion criteria: Diagnosis of CVID; based on recurrent respiratory tract infections, decreased total serum IgG (
Exclusion criteria
Exclusion criteria: Both patients groups: uncertainty about the diagnosis. Acute and/or severe infections at the moment of inclusion. XLA patients: existence of auto immune symptoms
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Quantification and characterisation of apoptosis in T and B cells 2. Quantification and functional determination of regulatory T cells 3. Function of the thymus | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. The differences in the 3 abovementioned outcome parameters between healthy controls, CVID patients and XLA control patients for both the pediatric and adult population. 2. The differences in the 3 abovementioned outcome parameters between subgroups of CVID patients, namely patients with and without auto immune symptoms, also within the pediatric and adult population. 3. Correlation between the function of the thymus and the amount of regulatory T cells. 4. Correlation between regulatory T cells and apoptosis. | — |
Countries
Netherlands
Outcome results
None listed