Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41467-019-08641-z
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dc.titleJapanese encephalitis virus neuropenetrance is driven by mast cell chymase
dc.contributor.authorHsieh, J.T.
dc.contributor.authorRathore, A.P.S.
dc.contributor.authorSoundarajan, G.
dc.contributor.authorSt. John, A.L.
dc.date.accessioned2022-01-07T03:49:51Z
dc.date.available2022-01-07T03:49:51Z
dc.date.issued2019
dc.identifier.citationHsieh, J.T., Rathore, A.P.S., Soundarajan, G., St. John, A.L. (2019). Japanese encephalitis virus neuropenetrance is driven by mast cell chymase. Nature Communications 10 (1) : 706. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-019-08641-z
dc.identifier.issn2041-1723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/213241
dc.description.abstractJapanese encephalitis virus (JEV) is a leading cause of viral encephalitis. However, the mechanisms of JEV penetration of the blood-brain-barrier (BBB) remain poorly understood. Mast cells (MCs) are granulated innate immune sentinels located perivascularly, including at the BBB. Here we show that JEV activates MCs, leading to the release of granule-associated proteases in vivo. MC-deficient mice display reduced BBB permeability during JEV infection compared to congenic wild-type (WT) mice, indicating that enhanced vascular leakage in the brain during JEV infection is MC-dependent. Moreover, MCs promoted increased JEV infection in the central nervous system (CNS), enhanced neurological deficits, and reduced survival in vivo. Mechanistically, chymase, a MC-specific protease, enhances JEV-induced breakdown of the BBB and cleavage of tight-junction proteins. Chymase inhibition reversed BBB leakage, reduced brain infection and neurological deficits during JEV infection, and prolonged survival, suggesting chymase is a novel therapeutic target to prevent JEV encephalitis. © 2019, The Author(s).
dc.publisherNature Publishing Group
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2019
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1038/s41467-019-08641-z
dc.description.sourcetitleNature Communications
dc.description.volume10
dc.description.issue1
dc.description.page706
dc.published.statePublished
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