2018
DOI: 10.3389/fmicb.2018.00692
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Corrigendum: Ebola VP40 in Exosomes Can Cause Immune Cell Dysfunction

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Cited by 2 publications
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“…Upon infection, EBOV primarily targets dendritic cells, monocytes, and macrophages, potentially facilitating systemic virus spread, including liver and secondary lymphoid organs [ 40 ]. Given the symptoms mentioned above and the high mortality rate of 80–90%, Ebola patients’ rapid identification is necessary [ 41 ]. A commonly applied technique for diagnosing Ebola patients is the detection of VP40, the EBOV matrix protein [ 39 ].…”
Section: Role Of Evs In the Pathogenesis Of Viral Infectionsmentioning
confidence: 99%
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“…Upon infection, EBOV primarily targets dendritic cells, monocytes, and macrophages, potentially facilitating systemic virus spread, including liver and secondary lymphoid organs [ 40 ]. Given the symptoms mentioned above and the high mortality rate of 80–90%, Ebola patients’ rapid identification is necessary [ 41 ]. A commonly applied technique for diagnosing Ebola patients is the detection of VP40, the EBOV matrix protein [ 39 ].…”
Section: Role Of Evs In the Pathogenesis Of Viral Infectionsmentioning
confidence: 99%
“…EBOV pathology is further enhanced by exosome-bound VP40 modulating RNAi components, such as Dicer and Ago 1, and inducing recipient naïve cell death while upregulating exosome biogenesis [ 41 ]. EBOV content release is not limited to exosomes but extends to microvesicles as well [ 38 ].…”
Section: Role Of Evs In the Pathogenesis Of Viral Infectionsmentioning
confidence: 99%