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HBV-induced microenvironment reduces pDC response to TLR9 stimulation

abstract in conference proceedings
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Author
Berehovska, Olena
Pimková Polidarová, MarkétaORCiD Profile - 0000-0003-3116-1328WoS Profile - V-2351-2017Scopus Profile - 57212310198
Janovec, VáclavORCiD Profile - 0000-0002-6262-3364WoS Profile - N-7608-2017Scopus Profile - 57193086112
Hirsch, IvanORCiD Profile - 0000-0003-1701-1438WoS Profile - R-3103-2016Scopus Profile - 56275056800
Grantz Šašková, KláraORCiD Profile - 0000-0003-2874-5699WoS Profile - E-1931-2014Scopus Profile - 22954587000
Kenes Group

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Publication date
2024
Published in
TOLL 2024 Road to translation
Publisher / Publication place
(Nizozemsko)
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  • Faculty of Science
Abstract
Hepatitis B virus (HBV) is a non-cytopathogenic virus with DNA genome. It causes an acute hepatitis that may develop into chronic hepatitis B, liver cirrhosis and hepatocellular carcinoma. HBV is described as "stealth virus" as it possesses various mechanisms of interference with immune recognition.We investigated the effect of HBV on activation of plasmacytoid dendritic cells (pDCs), as they are a main producer of interferon α (IFNα). IFNα secretion is induced by toll-like receptor 9 (TLR9) activation, yet this pathway is strictly regulated. One of the TLR9 pathway negative modulators is miRNA146a, which silences the TLR signalling proteins. Importantly, miRNA146a is active in the RNA-induced silencing complex (RISC), which binds the target mRNA and silences it. Mature miRNA-RISC can be sorted into extracellular vesicles (EVs) and transported to surrounding cells.Therefore, we analysed, whether HBV infection affects the quantity of miRNA-146a secreted from hepatocytes, and whether the secreted miRNA146a affects the pDC function.
Keywords
Chronic HBV, miRNA-146a, pDC,TLR9 signaling, extracellular vesicles
Permanent link
https://hdl.handle.net/20.500.14178/2422
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