Author:
Rossato Paolo,Federti Enrica,Matte Alessandro,Glantschnig Helmut,Canneva Fabio,Schuster Maria,Coulibaly Sogue,Schrenk Gerald,Voelkel Dirk,Dockal Michael,Plaimauer Barbara,Andolfo Immacolata,Iolascon Achille,Rottensteiner Hanspeter,Gritsch Herbert,Scheiflinger Friedrich,Hoellriegl Werner,Franceschi Lucia De
Abstract
Sickle cell disease (SCD) is an inherited red blood cell disorder that occurs worldwide. Acute vaso-occlusive crisis is the main cause of hospitalization in patients with SCD. There is growing evidence that inflammatory vasculopathy plays a key role in both acute and chronic SCD-related clinical manifestations. In a humanized mouse model of SCD, we found an increase of von Willebrand factor activity and a reduction in the ratio of a disintegrin and metalloproteinase with thrombospondin type 1 motif, number 13 (ADAMTS13) to von Willebrand factor activity similar to that observed in the human counterpart. Recombinant ADAMTS13 was administered to humanized SCD mice before they were subjected to hypoxia/reoxygenation (H/R) stress as a model of vaso-occlusive crisis. In SCD mice, recombinant ADAMTS13 reduced H/R-induced hemolysis and systemic and local inflammation in lungs and kidneys. It also diminished H/R-induced worsening of inflammatory vasculopathy, reducing local nitric oxidase synthase expression. Collectively, our data provide for the firsttime evidence that pharmacological treatment with recombinant ADAMTS13 (TAK-755) diminished H/R-induced sickle cell-related organ damage. Thus, recombinant ADAMTS13 might be considered as a potential effective disease-modifying treatment option for sickle cell-related acute events.
Publisher
Ferrata Storti Foundation (Haematologica)
Cited by
13 articles.
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