Thromb Haemost 1997; 77(01): 011-013
DOI: 10.1055/s-0038-1655728
Rapid Communication
Schattauer GmbH Stuttgart

Autoantibodies Against the Protease Inhibitor Calpastatin: A New Risk Factor for Venous Thrombosis?

Authors

  • Udo Schlosser

    The Institut für Klinische Chemie und Laboratoriumsmedizin, Universität Regensburg, Germany
  • Karl J Lackner

    The Institut für Klinische Chemie und Laboratoriumsmedizin, Universität Regensburg, Germany
  • Christine Scheckenhofer

    The Institut für Klinische Chemie und Laboratoriumsmedizin, Universität Regensburg, Germany
  • Michael Spannagl

    1   The Medizinische Klinik, Klinikum Innenstadt, Ludwig-Maximilians-Universität Munchen, Germany
  • Florentin A Spengel

    1   The Medizinische Klinik, Klinikum Innenstadt, Ludwig-Maximilians-Universität Munchen, Germany
  • Gabriele Hahn

    2   The Department of Microbiology and Immunology, Stanford University, Stanford, CA
  • Bernhard Lang

    3   The Klinik und Poliklinik fur Innere Medizin I, Universität Regensburg, Germany
  • Gerd Schmitz

    The Institut für Klinische Chemie und Laboratoriumsmedizin, Universität Regensburg, Germany
Further Information

Publication History

Received 18 April 1996

Accepted after resubmission 16 September 1996

Publication Date:
11 July 2018 (online)

Summary

Autoantibodies reactive against human calpastatin were detected by screening a cDNA expression library with the serum of a 53 year old white female patient with a history of venous thrombosis and suspected antiphospholipid syndrome. When further sera were analyzed it could be shown that >90% of calpastatin autoantibodies, detected by Western blotting against the partial calpastatin clone, react with the C-terminal amino acids of the protein. Therefore, an ELISA based on a synthetic peptide containing the C-terminal 27 amino acids of calpastatin was developed and 205 healthy blood donors and 138 random sera from hospital patients were analyzed. A total of 11 sera (3.2%) were positive with no significant difference between the two groups (7/205 and 4/138). In 80 consecutive patients with a history of venous thrombosis 9 positive sera (11.3%; p < 0.01 vs. blood donors, p<0.02 vs. hospital patients) were detected. Our results indicate that autoantibodies against calpastatin may constitute a so far unknown risk factor for venous thrombosis.