Defibrotide Interferes With Several Steps of the Coagulation-Inflammation Cycle and Exhibits Therapeutic Potential to Treat Severe Malaria


Autoria(s): Francischetti, Ivo M. B.; Oliveira, Carlo J.; Ostera, Graciela R.; Yager, Stephanie B.; Debierre-Grockiego, Francoise; Pereira, Vanessa Carregaro; Jaramillo-Gutierrez, Giovanna; Hume, Jen C. C.; Jiang, Lubin; Moretz, Samuel E.; Lin, Christina K.; Ribeiro, Jose M. C.; Long, Carole A.; Vickers, Brandi K.; Schwarz, Ralph T.; Seydel, Karl B.; Iacobelli, Massimo; Ackerman, Hans C.; Srinivasan, Prakash; Gomes, Regis B.; Wang, Xunde; Monteiro, Robson Q.; Kotsyfakis, Michail; Nunes, Anderson de Sá; Waisberg, Michael
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

21/10/2013

21/10/2013

2012

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

http://dx.doi.org/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