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Cited by 159

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Dengue Fever in Humanized NOD/SCID Mice

Open access
Bente, Dennis A., Melkus, Michael W., Garcia, J. Victor, Rico-Hesse, Rebeca·2005·Journal of Virology

Abstract

The increased transmission and geographic spread of dengue fever (DF) and its more severe presentation, dengue hemorrhagic fever (DHF), make it the most important mosquito-borne viral disease of humans (50 to 100 million infections/year) (World Health Organization, Fact sheet 117, 2002). There are no vaccines or treatment for DF or DHF because there are no animal or other models of human disease; even higher primates do not show symptoms after infection (W. F. Scherer, P. K. Russell, L. Rosen, J. Casals, and R. W. Dickerman, Am. J. Trop. Med. Hyg. 27: 590-599, 1978). We demonstrate that nonobese diabetic/severely compromised immunodeficient (NOD/SCID) mice xenografted with human CD34 + cells develop clinical signs of DF as in humans (fever, rash, and thrombocytopenia), when infected in a manner mimicking mosquito transmission (dose and mode). These results suggest this is a valuable model with which to study pathogenesis and test antidengue products.

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Metadata

Authors
Bente, D. A., Melkus, M. W., Garcia, J. V., & Rico-Hesse, R.
Venue
Journal of Virology
Published
2005-11
Volume
79
Issue
21
Pages
13797-13799
ISSN
  • 0022-538X (ISSN-L)
  • 1098-5514
OpenAlex
W2157908499
Cited by
159
References
0
FWCI
10.35
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Dengue Fever in Humanized NOD/SCID Mice. https://app.cochat.ai/papers/10.1128/jvi.79.21.13797-13799.2005
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Bente, D. A., Melkus, M. W., Garcia, J. V., & Rico-Hesse, R. (2005). Dengue Fever in Humanized NOD/SCID Mice. Journal of Virology. https://doi.org/10.1128/jvi.79.21.13797-13799.2005

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