Thromb Haemost 2005; 94(05): 933-941
DOI: 10.1160/TH05-04-0254
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Combinatorial peptides directed to inhibitory antibodies against human blood clotting factor VIII

Eva-Maria Kopecky
1   Department of Biotechnology, University of Natural Resources and Applied Life Sciences, Vienna, Austria
,
Sabine Greinstetter
1   Department of Biotechnology, University of Natural Resources and Applied Life Sciences, Vienna, Austria
,
Ingrid Pabinger
2   Department of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University Vienna, Austria
,
Andrea Buchacher
3   Octapharma Pharmazeutika Produktions Ges. mbH, Vienna, Austria
,
Jürgen Römisch
3   Octapharma Pharmazeutika Produktions Ges. mbH, Vienna, Austria
,
Alois Jungbauer
1   Department of Biotechnology, University of Natural Resources and Applied Life Sciences, Vienna, Austria
› Author Affiliations

Financial support: This work was financially supported by Austrian Research Promotion Agency Ltd. (FFG) project No. 808626
Further Information

Publication History

Received: 14 April 2005

Accepted after revision: 05 September 2005

Publication Date:
14 December 2017 (online)

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Summary

The development of antibodies against blood clotting factorVIII is a major complication affecting 20–30% of hemophilia A patients receiving replacement with FVIII concentrates. This study investigated generating peptides acting as broadly neutralizing agents to block factor VIII antibodies. These peptides were selected from dual positional scanning decapeptide libraries on cellulose membranes. From this library comprising 6.8×1012 peptides we selected 468 peptides for further screening rounds. Finally we identified two decapeptides with the ability to block 8 out of 10 inhibitory antibodies from sera of patients with FVIII inhibitors demonstrated by competition assays. Sequence alignment of the peptides showed similarity with several domains in the FVIII molecule demonstrating the mimotope nature of the selected peptides. Our results show the efficiency of the combinatorial library approach and show the potential of combinatorial peptides to compete out polyclonal inhibitor IgG from a broad range of patients’ sera. Combinatorial peptides could be novel and highly effective drug candidates for alternative treatment in patients with factor VIII inhibitors.