MPL and autoimmune thrombocytopenic purpura: A recent study showed that miR-221-3p is involved in the pathogenesis of primary immune thrombocytopenia (ITP) and is differentially expressed before and after treatment with thrombopoietin receptor agonists (TPO-RAs), indicating its value as a predictive marker of the platelet response to treatment with TPO-RA [30].