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Increased TNF-α Initiates Cytoplasmic Vacuolization in Whole Blood Coculture with Dengue Virus
Author(s) -
Rahmat Dani Satria,
TzuWen Huang,
Ming-Kai Jhan,
TingJing Shen,
PoChun Tseng,
Yunting Wang,
Zhenyu Yang,
ChungHsi Hsing,
ChiouFeng Lin
Publication year - 2021
Publication title -
journal of immunology research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.315
H-Index - 83
eISSN - 2314-8861
pISSN - 2314-7156
DOI - 10.1155/2021/6654617
Subject(s) - dengue virus , viremia , dengue fever , biology , vacuolization , ex vivo , cd14 , virology , immunology , immune system , virus , peripheral blood mononuclear cell , in vivo , in vitro , biochemistry , microbiology and biotechnology , endocrinology
During the acute febrile phase of dengue virus (DENV) infection, viremia can cause severe systemic immune responses accompanied by hematologic disorders. This study investigated the potential induction and mechanism of the cytopathic effects of DENV on peripheral blood cells ex vivo . At one day postinfection, there was viral nonstructural protein NS1 but no further virus replication measured in the whole blood culture. Notably, DENV exposure caused significant vacuolization in monocytic phagocytes. With a minor change in the complete blood cell count, except for a minor increase in neutrophils and a significant decrease in monocytes, the immune profiling assay identified several changes, particularly a significant reduction in CD14-positive monocytes as well as CD11c-positive dendritic cells. Abnormal production of TNF- α was highly associated with the induction of vacuolization. Manipulating TNF- α expression resulted in cytopathogenic effects. These results demonstrate the potential hematological damage caused by ex vivo DENV-induced TNF- α .

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