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- W2058756509 abstract "West Nile virus (WNV), a mosquito-transmitted single-stranded RNA (ssRNA) flavivirus, causes human disease of variable severity. We investigated Toll-like receptor 7-deficient (Tlr7−/−) and myeloid differentiation factor 88-deficient (Myd88−/−) mice, which both have defective recognition of ssRNA, and found increased viremia and susceptibility to lethal WNV infection. Despite increased tissue concentrations of most innate cytokines, CD45+ leukocytes and CD11b+ macrophages failed to home to WNV-infected cells and infiltrate into target organs of Tlr7−/− mice. Tlr7−/− mice and macrophages had reduced interleukin-12 (IL-12) and IL-23 responses after WNV infection, and mice deficient in IL-12 p40 and IL-23 p40 (Il12b−/−) or IL-23 p19 (Il23a−/−), but not IL-12 p35 (Il12a−/−), responded similarly to Tlr7−/− mice, with increased susceptibility to lethal WNV encephalitis. Collectively, these results demonstrate that TLR7 and IL-23-dependent WNV responses represent a vital host defense mechanism that operates by affecting immune cell homing to infected target cells." @default.
- W2058756509 created "2016-06-24" @default.
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- W2058756509 date "2009-02-01" @default.
- W2058756509 modified "2023-10-08" @default.
- W2058756509 title "Toll-like Receptor 7 Mitigates Lethal West Nile Encephalitis via Interleukin 23-Dependent Immune Cell Infiltration and Homing" @default.
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- W2058756509 doi "https://doi.org/10.1016/j.immuni.2008.11.012" @default.
- W2058756509 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2707901" @default.
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