Suppression of in vitro megakaryocyte production by antiplatelet autoantibodies from adult patients with chronic ITP

Blood. 2004 Feb 15;103(4):1364-9. doi: 10.1182/blood-2003-08-2672. Epub 2003 Oct 23.


Chronic immune thrombocytopenic purpura (ITP) is manifested by autoantibody-induced platelet destruction. Platelet turnover studies suggest that autoantibody may also affect platelet production. To evaluate this, we studied the effect of plasma from adult patients with chronic ITP on in vitro megakaryocyte production. CD34(+) cells, obtained from healthy donors, were cultured in medium containing PEG-rHuMGDF and 10% plasma from either ITP patients or healthy subjects. Cultures containing plasma from 12 of 18 ITP patients showed a significant decrease (26%-95%) in megakaryocyte production when compared with control cultures. Positive ITP plasmas not only reduced the total number of megakaryocytes produced during the culture period but also inhibited megakaryocyte maturation, resulting in fewer 4N, 8N, and 16N cells. The role of antibody in this suppression is supported by 2 factors: (1) immunoglobulin G (IgG) from ITP patients inhibited megakaryocyte production when compared with control IgG; and (2) adsorption of autoantibody, using immobilized antigen, resulted in significantly less inhibition of megakaryocyte production when compared with unadsorbed plasma. These results show that plasma autoantibody from some adult patients with ITP inhibits in vitro megakaryocyte production, suggesting that a similar effect may occur in vivo.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Antigens, CD34 / analysis
  • Autoantibodies / blood
  • Autoantibodies / immunology*
  • Blood Platelets / immunology*
  • Cell Culture Techniques / methods
  • Cells, Cultured
  • Chronic Disease
  • Hematopoiesis / immunology
  • Humans
  • Leukapheresis
  • Megakaryocytes / chemistry
  • Megakaryocytes / cytology*
  • Megakaryocytes / immunology*
  • Ploidies
  • Purpura, Thrombocytopenic, Idiopathic / immunology*


  • Antigens, CD34
  • Autoantibodies