Host Response Dynamics Following Lethal Infection of Rhesus Macaques With Zaire ebolavirus

被引:84
作者
Ebihara, Hideki [1 ]
Rockx, Barry [1 ]
Marzi, Andrea [1 ]
Feldmann, Friederike [2 ]
Haddock, Elaine [1 ]
Brining, Douglas [3 ]
LaCasse, Rachel A. [3 ]
Gardner, Don [3 ]
Feldmann, Heinz [1 ]
机构
[1] NIAID, Virol Lab, NIH, Rocky Mt Labs, Hamilton, MT 59840 USA
[2] NIAID, Off Res Operat, NIH, Rocky Mt Labs, Hamilton, MT 59840 USA
[3] NIAID, Rocky Mt Vet Branch, Div Intramural Res, NIH,Rocky Mt Labs, Hamilton, MT 59840 USA
基金
美国国家卫生研究院;
关键词
HEMORRHAGIC-FEVER; DENDRITIC CELLS; PROTEIN-C; POSTEXPOSURE PROTECTION; COAGULATION DISORDERS; VIRUS-INFECTION; PATHOGENESIS; MARBURG; SEPSIS; INNATE;
D O I
10.1093/infdis/jir336
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To gain further insight into the interdependent pathogenic processes in Ebola hemorrhagic fever (EHF), we have examined the dynamics of host responses in individual rhesus macaques infected with Zaire ebolavirus over the entire disease course. Examination of coagulation parameters revealed that decreased coagulation inhibitor activity triggered severe coagulopathy as indicated by prolonged coagulation times and decreased fibrinogen levels. This has been proposed as one of the significant mechanisms underlying disseminated intravascular coagulation in EHF patients. Furthermore, monitoring of expression levels for cytokines/chemokines suggested a mixed anti-inflammatory response syndrome (MARS), which indicates that a catastrophic uncontrolled immunological status contributes to the development of fatal hemorrhagic fever. These results highlight the pathological analogies between EHF and severe sepsis and not only contribute to our understanding of the pathogenic process, but will also help to establish novel postexposure treatment modalities.
引用
收藏
页码:S991 / S999
页数:9
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