A novel immunocompetent transgenic mouse model of DHF reveals Syk-mediated Th2-polarized cytokine storm as a key driver of vascular leakage

Dengue virus (DENV) infection remains a critical global health threat, with DENV-2 being the most virulent serotype capable of causing lethal dengue hemorrhagic fever (DHF), a severe complication characterized by plasma leakage and hemorrhagic manifestations. While the search for viral receptors and...

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Published inEmerging microbes & infections Vol. 14; no. 1; p. 2531178
Main Authors Wang, YuYa, Yang, Wei, Yang, YuanSong, Cheng, HuiHui, Xiong, Rui, Wu, Xi, Xu, Nan, Liu, ShuNan, Qu, Zhe, Ling, Chen, Cao, Yuan, Yang, Yanwei, Zhao, HaoYang, Gu, WenDa, Wu, Yong, Liu, SuSu, Wang, Yining, Wang, Yu, Wang, SanLong, Fu, Rui, Huang, WeiJin, Zhou, Hongning, Wei, Wei, An, Jing, Wang, YouChun, Fan, ChangFa
Format Journal Article
LanguageEnglish
Published United States Taylor & Francis 31.12.2025
Taylor & Francis Group
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Online AccessGet full text
ISSN2222-1751
2222-1751
DOI10.1080/22221751.2025.2531178

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Abstract Dengue virus (DENV) infection remains a critical global health threat, with DENV-2 being the most virulent serotype capable of causing lethal dengue hemorrhagic fever (DHF), a severe complication characterized by plasma leakage and hemorrhagic manifestations. While the search for viral receptors and immunocompetent animal models has persisted since the first recorded outbreak in 1779, significant gaps remain. Here, we establish the first immunocompetent murine model of DHF with intact innate/adaptive immunity by generating hTim4-transgenic C57BL/6J mice. This model recapitulates fatal DHF complications seen in humans, including systemic hemorrhage, dengue encephalitis and intestinal ischemia/gangrene. Integrated single-cell RNA sequencing and spatial transcriptomics analysis of hemorrhagic gut lesions demonstrated that DENV-2 infection induces Syk protein overexpression, leading to enhanced Th2 cytokine secretion and impaired hemostatic regulation. This cascade enhances vascular permeability, promotes plasma leakage, and drives multiorgan hemorrhage, a mechanism corroborated by parallel analyses of human DHF tissues. Critically, Th2-biased cytokine storm mirrors clinical findings in severe human dengue cases. Our work not only identifies hTim4 as a functional DENV-2 receptor but also provides a mechanistically grounded platform for DHF pathogenesis studies, bridging critical gaps between preclinical models and human immunopathology.
AbstractList Dengue virus (DENV) infection remains a critical global health threat, with DENV-2 being the most virulent serotype capable of causing lethal dengue hemorrhagic fever (DHF), a severe complication characterized by plasma leakage and hemorrhagic manifestations. While the search for viral receptors and immunocompetent animal models has persisted since the first recorded outbreak in 1779, significant gaps remain. Here, we establish the first immunocompetent murine model of DHF with intact innate/adaptive immunity by generating hTim4-transgenic C57BL/6J mice. This model recapitulates fatal DHF complications seen in humans, including systemic hemorrhage, dengue encephalitis and intestinal ischemia/gangrene. Integrated single-cell RNA sequencing and spatial transcriptomics analysis of hemorrhagic gut lesions demonstrated that DENV-2 infection induces Syk protein overexpression, leading to enhanced Th2 cytokine secretion and impaired hemostatic regulation. This cascade enhances vascular permeability, promotes plasma leakage, and drives multiorgan hemorrhage, a mechanism corroborated by parallel analyses of human DHF tissues. Critically, Th2-biased cytokine storm mirrors clinical findings in severe human dengue cases. Our work not only identifies hTim4 as a functional DENV-2 receptor but also provides a mechanistically grounded platform for DHF pathogenesis studies, bridging critical gaps between preclinical models and human immunopathology.
Dengue virus (DENV) infection remains a critical global health threat, with DENV-2 being the most virulent serotype capable of causing lethal dengue hemorrhagic fever (DHF), a severe complication characterized by plasma leakage and hemorrhagic manifestations. While the search for viral receptors and immunocompetent animal models has persisted since the first recorded outbreak in 1779, significant gaps remain. Here, we establish the first immunocompetent murine model of DHF with intact innate/adaptive immunity by generating hTim4-transgenic C57BL/6J mice. This model recapitulates fatal DHF complications seen in humans, including systemic hemorrhage, dengue encephalitis and intestinal ischemia/gangrene. Integrated single-cell RNA sequencing and spatial transcriptomics analysis of hemorrhagic gut lesions demonstrated that DENV-2 infection induces Syk protein overexpression, leading to enhanced Th2 cytokine secretion and impaired hemostatic regulation. This cascade enhances vascular permeability, promotes plasma leakage, and drives multiorgan hemorrhage, a mechanism corroborated by parallel analyses of human DHF tissues. Critically, Th2-biased cytokine storm mirrors clinical findings in severe human dengue cases. Our work not only identifies hTim4 as a functional DENV-2 receptor but also provides a mechanistically grounded platform for DHF pathogenesis studies, bridging critical gaps between preclinical models and human immunopathology.Dengue virus (DENV) infection remains a critical global health threat, with DENV-2 being the most virulent serotype capable of causing lethal dengue hemorrhagic fever (DHF), a severe complication characterized by plasma leakage and hemorrhagic manifestations. While the search for viral receptors and immunocompetent animal models has persisted since the first recorded outbreak in 1779, significant gaps remain. Here, we establish the first immunocompetent murine model of DHF with intact innate/adaptive immunity by generating hTim4-transgenic C57BL/6J mice. This model recapitulates fatal DHF complications seen in humans, including systemic hemorrhage, dengue encephalitis and intestinal ischemia/gangrene. Integrated single-cell RNA sequencing and spatial transcriptomics analysis of hemorrhagic gut lesions demonstrated that DENV-2 infection induces Syk protein overexpression, leading to enhanced Th2 cytokine secretion and impaired hemostatic regulation. This cascade enhances vascular permeability, promotes plasma leakage, and drives multiorgan hemorrhage, a mechanism corroborated by parallel analyses of human DHF tissues. Critically, Th2-biased cytokine storm mirrors clinical findings in severe human dengue cases. Our work not only identifies hTim4 as a functional DENV-2 receptor but also provides a mechanistically grounded platform for DHF pathogenesis studies, bridging critical gaps between preclinical models and human immunopathology.
Author Ling, Chen
Xiong, Rui
Wang, Yining
Wang, SanLong
Yang, Yanwei
An, Jing
Xu, Nan
Yang, Wei
Gu, WenDa
Liu, SuSu
Zhou, Hongning
Zhao, HaoYang
Liu, ShuNan
Cao, Yuan
Wu, Yong
Qu, Zhe
Wang, Yu
Wei, Wei
Cheng, HuiHui
Huang, WeiJin
Wang, YouChun
Wang, YuYa
Fu, Rui
Yang, YuanSong
Wu, Xi
Fan, ChangFa
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Issue 1
Keywords dengue hemorrhagic fever
th2-bias
cytokine storm
Dengue virus
Htim4 receptor
hemorrhage
Language English
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Snippet Dengue virus (DENV) infection remains a critical global health threat, with DENV-2 being the most virulent serotype capable of causing lethal dengue...
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SubjectTerms AC-Dengue Fever
Animals
Capillary Permeability
Cytokine Release Syndrome - immunology
Cytokine Release Syndrome - virology
cytokine storm
Cytokines - immunology
Cytokines - metabolism
dengue hemorrhagic fever
Dengue virus
Dengue Virus - immunology
Dengue Virus - physiology
Disease Models, Animal
Female
hemorrhage
Htim4 receptor
Humans
Mice
Mice, Inbred C57BL
Mice, Transgenic
Severe Dengue - genetics
Severe Dengue - immunology
Severe Dengue - pathology
Severe Dengue - virology
Syk Kinase - genetics
Syk Kinase - immunology
Syk Kinase - metabolism
Th2 Cells - immunology
th2-bias
Title A novel immunocompetent transgenic mouse model of DHF reveals Syk-mediated Th2-polarized cytokine storm as a key driver of vascular leakage
URI https://www.ncbi.nlm.nih.gov/pubmed/40623122
https://www.proquest.com/docview/3228020491
https://pubmed.ncbi.nlm.nih.gov/PMC12291195
https://doaj.org/article/f8438f51ec4a4667bec00685168aa031
Volume 14
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