Platelet activation and platelet-erythrocyte aggregates in patients with sickle cell anemia

J Lab Clin Med. 1997 May;129(5):507-16. doi: 10.1016/s0022-2143(97)90005-6.

Abstract

Vascular occlusion and vasculopathy underlie much of the morbidity in patients with sickle cell anemia. Platelets may play a role in this vasculopathy. Samples from 12 adults patients with sickle cell anemia were examined for evidence of platelet activation and formation of platelet-erythrocyte aggregates (PEA) using fluorescent-labeled monoclonal antibodies and flow cytometry. We noted an increased expression of activation-dependent antigens on the platelets from patients with sickle cell anemia compared with those from both white and black control subjects. In addition, patients with sickle cell anemia had increased levels of platelet microparticles and PEA. Platelets are activated in patients with sickle cell anemia and they adhere to sickle erythrocytes. The significance of this activation and adherence are the subject of further investigation.

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Anemia, Sickle Cell / blood*
  • Anemia, Sickle Cell / pathology
  • Blood Platelets / metabolism
  • Blood Platelets / ultrastructure
  • Cell Adhesion
  • Erythrocyte Aggregation*
  • Erythrocytes, Abnormal / metabolism
  • Erythrocytes, Abnormal / ultrastructure
  • Female
  • Flow Cytometry
  • Humans
  • In Vitro Techniques
  • Male
  • Microscopy, Electron
  • Middle Aged
  • Platelet Activation*
  • Platelet Aggregation*