Please use this identifier to cite or link to this item: https://doi.org/10.1128/JVI.01066-18
Title: Enterovirus a71 infection activates human immune responses and induces pathological changes in humanized mice
Authors: Ke, Y
Liu, WN 
Her, Z
Liu, M
Tan, SY
Tan, YW
Chan, XY
Fan, Y
Huang, EK
Chen, H
Chang, KTE 
Chan, JKY 
Chu, JJH 
Chen, Q
Keywords: enterovirus A71
human immune responses
humanized mice
Animals
CD8-Positive T-Lymphocytes
Cells, Cultured
Enterovirus A, Human
Enterovirus Infections
Fetus
Humans
Inflammation Mediators
Mice
Mice, Inbred NOD
Mice, SCID
Viral Load
Issue Date: 1-Feb-2019
Publisher: American Society for Microbiology
Citation: Ke, Y, Liu, WN, Her, Z, Liu, M, Tan, SY, Tan, YW, Chan, XY, Fan, Y, Huang, EK, Chen, H, Chang, KTE, Chan, JKY, Chu, JJH, Chen, Q (2019-02-01). Enterovirus a71 infection activates human immune responses and induces pathological changes in humanized mice. Journal of Virology 93 (3). ScholarBank@NUS Repository. https://doi.org/10.1128/JVI.01066-18
Abstract: © 2019 American Society for Microbiology. Since the discovery of enterovirus A71 (EV-A71) half a century ago, it has been recognized as the cause of large-scale outbreaks of hand-foot-and-mouth disease worldwide, particularly in the Asia-Pacific region, causing great concern for public health and economic burdens. Detailed mechanisms on the modulation of immune responses after EV-A71 infection have not been fully known, and the lack of appropriate models hinders the development of promising vaccines and drugs. In the present study, NOD-scid IL2R/(NSG) mice with a human immune system (humanized mice) at the age of 4 weeks were found to be susceptible to a human isolate of EV-A71 infection. After infection, humanized mice displayed limb weakness, which is similar to the clinical features found in some of the EV-A71-infected patients. Histopathological examination indicated the presence of vacuolation, gliosis, or meningomyelitis in brain stem and spinal cord, which were accompanied by high viral loads detected in these organs. The numbers of activated human CD4 and CD8T cells were upregulated after EV-A71 infection, and EV-A71-specific human T cell responses were found. Furthermore, the secretion of several proinflammatory cytokines, such as human gamma interferon (IFN-), interleukin-8 (IL-8), and IL-17A, was elevated in the EV-A71-infected humanized mice. Taken together, our results suggested that the humanized mouse model permits insights into the human immune responses and the pathogenesis of EV-A71 infection, which may provide a platform for the evaluation of anti-EV-A71 drug candidates in the future.
Source Title: Journal of Virology
URI: https://scholarbank.nus.edu.sg/handle/10635/173251
ISSN: 0022538X
10985514
DOI: 10.1128/JVI.01066-18
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