Anti-prothrombin antibodies cause thrombosis in a novel qualitative ex-vivo animal model

S. Haj-Yahja, Y. Sherer, M. Blank, H. Kaetsu, A. Smolinsky, Y. Shoenfeld

Research output: Contribution to journalArticlepeer-review

Abstract

Anti-prothrombin antibodies (aPT) are associated with thrombotic manifestations, and their association with reproductive failure is debatable. The aim of this study was to examine whether aPT could induce thrombosis and other clinical manifestations of the anti-phospholipid syndrome (APS). Mice were immunized with either prothrombin, β2-glycoprotein-I (β2GPI), or β2GPI followed by prothrombin. The presence of clinical manifestation of APS, including thrombocytopenia, lupus anticoagulant and fetal resorption rates, was evaluated in all mice groups compared with nonimmunized mice. Thrombosis was studied in a novel ex-vivo model in which the aorta was sutured for 1 min and the presence or absence of visible thrombus was qualitatively evaluated. Immunized mice developed high autoantibody levels directed towards their immunizing autoantigens. The groups immunized with β2GPI or β2GPI/prothrombin, but not with prothrombin alone, developed prolonged aPTT, thrombocytopenia and increased fetal resorption rate. All prothrombin-immunized mice as well as most β2GPI/prothrombin-immunized mice developed visible thrombus within the aorta. Some β2GPI immunized mice developed very mild thrombus. None of the CFA/PBS-injected or the nonimmunized mice developed such thrombus. Active immunization with prothrombin or β2GPI/prothrombin is associated with prothrombotic activity of blood in an ex-vivo model. This is the first direct evidence for thrombus induction by aPT.

Original languageEnglish
Pages (from-to)364-369
Number of pages6
JournalLupus
Volume12
Issue number5
DOIs
StatePublished - 2003
Externally publishedYes

Keywords

  • Anti-phospholipid antibody
  • Anti-phospholipid syndrome
  • Prothrombin
  • Thrombosis

Fingerprint

Dive into the research topics of 'Anti-prothrombin antibodies cause thrombosis in a novel qualitative ex-vivo animal model'. Together they form a unique fingerprint.

Cite this