Single‐cell sequencing reveals the features of adaptive immune responses in the liver of a mouse model of dengue fever

Abstract Background Dengue fever, an acute insect‐borne infectious disease caused by the dengue virus (DENV), poses a great challenge to global public health. Hepatic involvement is the most common complication of severe dengue and is closely related to the occurrence and development of disease. How...

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Main Authors: Yizhen Yuan, Qian Chen, Zhe Li, Fangzhou Cai, Dan Li, Wei Wang
Format: Article
Language:English
Published: Wiley 2025-01-01
Series:Animal Models and Experimental Medicine
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Online Access:https://doi.org/10.1002/ame2.12454
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author Yizhen Yuan
Qian Chen
Zhe Li
Fangzhou Cai
Dan Li
Wei Wang
author_facet Yizhen Yuan
Qian Chen
Zhe Li
Fangzhou Cai
Dan Li
Wei Wang
author_sort Yizhen Yuan
collection DOAJ
description Abstract Background Dengue fever, an acute insect‐borne infectious disease caused by the dengue virus (DENV), poses a great challenge to global public health. Hepatic involvement is the most common complication of severe dengue and is closely related to the occurrence and development of disease. However, the features of adaptive immune responses associated with liver injury in severe dengue are not clear. Methods We used single‐cell sequencing to examine the liver tissues of mild or severe dengue mice model to analyze the changes in immune response of T cells in the liver after dengue virus infection, and the immune interaction between macrophages and T cells. Flow cytometry was used to detect T cells and macrophages in mouse liver and blood to verify the single‐cell sequencing results. Results Our result showed CTLs were significantly activated in the severe liver injury group but the immune function‐related signal pathway was down‐regulated. The reason may be that the excessive immune response in the severe group at the late stage of DENV infection induces the polarization of macrophages into M2 type, and the macrophages then inhibit T cell immunity through the TGF‐β signaling pathway. In addition, the increased proportion of Treg cells suggested that Th17/Treg homeostasis was disrupted in the livers of severe liver injury mice. Conclusions In this study, single‐cell sequencing and flow cytometry revealed the characteristic changes of T cell immune response and the role of macrophages in the liver of severe dengue fever mice. Our study provides a better understanding of the pathogenesis of liver injury in dengue fever patients.
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spelling doaj-art-1eb9152fbe484bda9682220ec1cf293e2025-02-06T03:52:55ZengWileyAnimal Models and Experimental Medicine2576-20952025-01-0181304310.1002/ame2.12454Single‐cell sequencing reveals the features of adaptive immune responses in the liver of a mouse model of dengue feverYizhen Yuan0Qian Chen1Zhe Li2Fangzhou Cai3Dan Li4Wei Wang5National Center of Technology Innovation for Animal Model, State Key Laboratory of Respiratory Health and Multimorbidity, Key Laboratory of Pathogen Infection Prevention and Control (Peking Union Medical College), Ministry of Education, NHC Key Laboratory of Comparative Medicine Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences (CAMS) & Peking Union Medical College (PUMC) Beijing ChinaNational Center of Technology Innovation for Animal Model, State Key Laboratory of Respiratory Health and Multimorbidity, Key Laboratory of Pathogen Infection Prevention and Control (Peking Union Medical College), Ministry of Education, NHC Key Laboratory of Comparative Medicine Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences (CAMS) & Peking Union Medical College (PUMC) Beijing ChinaNational Center of Technology Innovation for Animal Model, State Key Laboratory of Respiratory Health and Multimorbidity, Key Laboratory of Pathogen Infection Prevention and Control (Peking Union Medical College), Ministry of Education, NHC Key Laboratory of Comparative Medicine Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences (CAMS) & Peking Union Medical College (PUMC) Beijing ChinaNational Center of Technology Innovation for Animal Model, State Key Laboratory of Respiratory Health and Multimorbidity, Key Laboratory of Pathogen Infection Prevention and Control (Peking Union Medical College), Ministry of Education, NHC Key Laboratory of Comparative Medicine Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences (CAMS) & Peking Union Medical College (PUMC) Beijing ChinaNational Center of Technology Innovation for Animal Model, State Key Laboratory of Respiratory Health and Multimorbidity, Key Laboratory of Pathogen Infection Prevention and Control (Peking Union Medical College), Ministry of Education, NHC Key Laboratory of Comparative Medicine Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences (CAMS) & Peking Union Medical College (PUMC) Beijing ChinaNational Center of Technology Innovation for Animal Model, State Key Laboratory of Respiratory Health and Multimorbidity, Key Laboratory of Pathogen Infection Prevention and Control (Peking Union Medical College), Ministry of Education, NHC Key Laboratory of Comparative Medicine Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences (CAMS) & Peking Union Medical College (PUMC) Beijing ChinaAbstract Background Dengue fever, an acute insect‐borne infectious disease caused by the dengue virus (DENV), poses a great challenge to global public health. Hepatic involvement is the most common complication of severe dengue and is closely related to the occurrence and development of disease. However, the features of adaptive immune responses associated with liver injury in severe dengue are not clear. Methods We used single‐cell sequencing to examine the liver tissues of mild or severe dengue mice model to analyze the changes in immune response of T cells in the liver after dengue virus infection, and the immune interaction between macrophages and T cells. Flow cytometry was used to detect T cells and macrophages in mouse liver and blood to verify the single‐cell sequencing results. Results Our result showed CTLs were significantly activated in the severe liver injury group but the immune function‐related signal pathway was down‐regulated. The reason may be that the excessive immune response in the severe group at the late stage of DENV infection induces the polarization of macrophages into M2 type, and the macrophages then inhibit T cell immunity through the TGF‐β signaling pathway. In addition, the increased proportion of Treg cells suggested that Th17/Treg homeostasis was disrupted in the livers of severe liver injury mice. Conclusions In this study, single‐cell sequencing and flow cytometry revealed the characteristic changes of T cell immune response and the role of macrophages in the liver of severe dengue fever mice. Our study provides a better understanding of the pathogenesis of liver injury in dengue fever patients.https://doi.org/10.1002/ame2.12454adaptive immunitydengue fever modelliver injurysingle‐cell sequencing
spellingShingle Yizhen Yuan
Qian Chen
Zhe Li
Fangzhou Cai
Dan Li
Wei Wang
Single‐cell sequencing reveals the features of adaptive immune responses in the liver of a mouse model of dengue fever
Animal Models and Experimental Medicine
adaptive immunity
dengue fever model
liver injury
single‐cell sequencing
title Single‐cell sequencing reveals the features of adaptive immune responses in the liver of a mouse model of dengue fever
title_full Single‐cell sequencing reveals the features of adaptive immune responses in the liver of a mouse model of dengue fever
title_fullStr Single‐cell sequencing reveals the features of adaptive immune responses in the liver of a mouse model of dengue fever
title_full_unstemmed Single‐cell sequencing reveals the features of adaptive immune responses in the liver of a mouse model of dengue fever
title_short Single‐cell sequencing reveals the features of adaptive immune responses in the liver of a mouse model of dengue fever
title_sort single cell sequencing reveals the features of adaptive immune responses in the liver of a mouse model of dengue fever
topic adaptive immunity
dengue fever model
liver injury
single‐cell sequencing
url https://doi.org/10.1002/ame2.12454
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