Idiopathic thrombocytopenic purpura (ITP) is the most frequent auto-immune cytopenia. There is no specific biological marker and the diagnosis often results from the exclusion of other differential diagnoses, notably inherited thrombocytopenia. Recent studies have reported an original platelet destruction mechanism in ITP, by antibody-mediated desialylation of membrane proteins. The detection of platelet sialylation can be readily achieved using flow cytometry. This could provide a new biomarker of ITP, useful to ascertain a diagnosis of ITP and guide towards proper patient management.
Study Type
OBSERVATIONAL
Enrollment
40
non interventional study
Nantes University Hospital
Nantes, France
Assess the difference of sialylation between ITP patients and other causes of thrombocytopenia / controls
a significant decrease in platelets sialylation in ITP patients, measured in flow cytometry with fluorescent Ricinus communis agglutinin
Time frame: 18 months
Prognostic value and therapy
prognostic value of the level of sialylation in ITP patients regarding disease evolution and response of first line treatments and splenectomy.
Time frame: 18 months
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