Defibrotide Interferes With Several Steps of the Coagulation-Inflammation Cycle and Exhibits Therapeutic Potential to Treat Severe Malaria
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
21/10/2013
21/10/2013
2012
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Resumo |
Objective-The coagulation-inflammation cycle has been implicated as a critical component in malaria pathogenesis. Defibrotide (DF), a mixture of DNA aptamers, displays anticoagulant, anti-inflammatory, and endothelial cell (EC)-protective activities and has been successfully used to treat comatose children with veno-occlusive disease. DF was investigated here as a drug to treat cerebral malaria. Methods and Results-DF blocks tissue factor expression by ECs incubated with parasitized red blood cells and attenuates prothrombinase activity, platelet aggregation, and complement activation. In contrast, it does not affect nitric oxide bioavailability. We also demonstrated that Plasmodium falciparum glycosylphosphatidylinositol (Pf-GPI) induces tissue factor expression in ECs and cytokine production by dendritic cells. Notably, dendritic cells, known to modulate coagulation and inflammation systemically, were identified as a novel target for DF. Accordingly, DF inhibits Toll-like receptor ligand-dependent dendritic cells activation by a mechanism that is blocked by adenosine receptor antagonist (8-p-sulfophenyltheophylline) but not reproduced by synthetic poly-A, -C, -T, and -G. These results imply that aptameric sequences and adenosine receptor mediate dendritic cells responses to the drug. DF also prevents rosetting formation, red blood cells invasion by P. falciparum and abolishes oocysts development in Anopheles gambiae. In a murine model of cerebral malaria, DF affected parasitemia, decreased IFN-gamma levels, and ameliorated clinical score (day 5) with a trend for increased survival. Conclusion-Therapeutic use of DF in malaria is proposed. (Arterioscler Thromb Vasc Biol. 2012; 32:786-798.) Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health DFG, Bonn, Germany [SCHW 296/18-2] DFG, Bonn, Germany Brazilian Malaria Network [MCT/CNPq/MS/SCTIE/DECIT/PRONEX 555648/2009-5] Brazilian Malaria Network National Academy of Sciences of the Czech Republic National Academy of Sciences of the Czech Republic [Z60220518] |
Identificador |
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, PHILADELPHIA, v. 32, n. 3, supl. 1, Part 2, pp. 786-U575, MAR, 2012 1079-5642 http://www.producao.usp.br/handle/BDPI/35239 10.1161/ATVBAHA.111.240291 |
Idioma(s) |
eng |
Publicador |
LIPPINCOTT WILLIAMS & WILKINS PHILADELPHIA |
Relação |
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY |
Direitos |
closedAccess Copyright LIPPINCOTT WILLIAMS & WILKINS |
Palavras-Chave | #ANTICOAGULANTS #BLOOD COAGULATION #ENDOTHELIUM #MICROCIRCULATION #VASCULAR BIOLOGY #FALCIPARUM-INFECTED ERYTHROCYTES #FACTOR PATHWAY INHIBITOR #INNATE IMMUNE-RESPONSE #DENDRITIC CELLS #VENOOCCLUSIVE DISEASE #ADENOSINE RECEPTORS #BLOOD-COAGULATION #ENDOTHELIAL-CELLS #IXODES-SCAPULARIS #CEREBRAL MALARIA #HEMATOLOGY #PERIPHERAL VASCULAR DISEASE |
Tipo |
article original article publishedVersion |