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Dengue Fever in Humanized NOD/SCID Mice
Open accessAbstract
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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Cited by
Agarwal, Y., Beatty, C., Ho, S., Thurlow, L., Das, A., Kelly, S., Castronova, I., Salunke, R., Biradar, S., Yeshi, T., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-71548-z · Cited by 38
What we are learning on HTLV-1 pathogenesis from animal models
Dodon, M. D., Villaudy, J., Gazzolo, L., Haines, R., & Lairmore, M. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00320 · Cited by 23
Metadata
- Authors
- Bente, D. A., Melkus, M. W., Garcia, J. V., & Rico-Hesse, R.
- Venue
- Journal of Virology
- Publisher
- American Society for Microbiology
- 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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- 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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