4.7 Article

Dengue virus-induced hemorrhage in a nonhuman primate model

期刊

BLOOD
卷 115, 期 9, 页码 1823-1834

出版社

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2009-09-242990

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资金

  1. U19 Pilot Project Funds [RFA-AI-02-042]
  2. National Institutes of Health/SERCEB
  3. Emory URC
  4. Yerkes National Primate Research Center [DRR000165]

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Lack of a dengue hemorrhagic animal model recapitulating human dengue virus infection has been a significant impediment in advancing our understanding of the early events involved in the pathogenesis of dengue disease. In efforts to address this issue, a group of rhesus macaques were intravenously infected with dengue virus serotype 2 (strain 16 681) at 1 x 10(7) PFU/animal. A classic dengue hemorrhage developed 3 to 5 days after infection in 6 of 6 animals. Blood chemistry appeared to be normal with exception of creatine phosphokinase, which peaked at 7 days after infection. A modest thrombocytopenia and noticeable neutropenia concomitant with slight decrease of hemoglobin and hematocrit were registered. In addition, the concentration of D-dimer was elevated significantly. Viremia peaked at 3 to 5 days after infection followed by an inverse relationship between T and B lymphocytes and a bimodal pattern for platelet-monocytes and platelet-neutrophil aggregates. Dengue virus containing platelets engulfed by monocytes was noted at 8 or 9 days after infection. Thus, rhesus macaques inoculated intravenously with a high dose of dengue virus produced dengue hemorrhage, which may provide a unique platform to define the early events in dengue virus infection and help identify which blood components contribute to the pathogenesis of dengue disease. (Blood. 2010;115:1823-1834)

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