Waldenström Macroglobulinemia
Conditions
Brief summary
Waldenström's macroglobulinemia is a rare disease whose pathophysiology remains at present poorly understood, although a recurrent mutation (L265P MYD88) has recently been described. Unlike other lymphoproliferative disorders, there is a defect in isotype switching, mechanism involving AID and NHEJ complex. Using a two-dimensional electrophoresis technology, our group showed that MW had a specific proteomic profile, and one of the differentially expressed proteins is Ku70 (encoded by XRCC6 belonging to NHEJ complex) . The investigators purpose to explore the mechanisms of underexpression of Ku70/XRCC6 (genetic or epigenetic modification) in comparison with other lymphoid malignancies and normal B cells.
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
* Patient over 18 years, affiliated to the social regimen * Written consent collected MW group : * Patient with a diagnosis of MW according to WHO criteria (based on the results of serum protein electrophoresis, bone marrow analysis with immunophenotyping, cytogenetic analysis and mutation L265P MyD88) Other SLP : * Patient with diagnosis of Chronic Lymphocytic Leukemia, Splenic Marginal Zone Lymphoma or Multiple Myeloma Healthy volunteers : * volunteers without blood disorders
Exclusion criteria
* Women of childbearing age who do not have an effective means of contraception * Pregnant or nursing * Demonstration of a kappa or lambda monotype on B lymphocytes * healthy volunteer with B-cell malignancy
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Measure of ratio Ku70/XRCC6 | Baseline | Comparing the average level of expression of Ku70 in B cells measured in patients of WM, in patients other SLP and in healthy subjects (without MW and other SLP) , matched for age ( +/- 5 years) and sex |
Countries
France