Summary
Thrombopoietin receptor agonists (TPO-RA) have recently been introduced for the treatment
of immune thrombocytopenia (ITP), an antiplatelet-antibodies autoimmune disease. The
observation of a low frequency of bleeding episodes despite their thrombocytopenia
suggests the existence of a compensatory mechanism. This study aimed to evaluate the
effect of TPO-RA treatment on platelet function and on the procoagulant state in ITP
patients before (ITP-bR) and after responding (ITP-aR) to treatment. Plasma- and microparticle
(MP)-associated procoagulant capacity from ITP patients was similar before and after
responding to the TPO-RA regimen but higher than the healthy control values. High
MP-associated procoagulant activity did not seem to be due to increased platelet activation,
since platelet stimulation by agonists was reduced in ITP-bR and ITP-aR patients.
It could be related to increased platelet apoptosis, evaluated in terms of surface
phosphatidylserine (PS), observed in both ITP groups. In summary, TPO-RA treatment
increased platelet count but did not ameliorate their function and did not change
plasma- and MP-associated procoagulant state of ITP patient responders to this therapy.
Keywords
Thrombopoietin receptor agonists - platelets - thrombin generation - microparticle-associated
procoagulant state