Department of Pathology, University of Texas Medical Branch (UTMB), Galveston, TX 77555, USA.
Department of Microbiology and Immunology, UTMB, Galveston, TX, USA.
Virology. 2014 Feb;450-451:278-89. doi: 10.1016/j.virol.2013.12.021. Epub 2014 Jan 10.
Macrophages encounter flaviviruses early after injection by arthropod vectors. Using in vivo imaging of mice inoculated with firefly luciferase-expressing single-cycle flavivirus particles (FLUC-SCFV), we examined the initial dissemination of virus particles in the presence or absence of lymph node (LN)-resident macrophages. Higher luciferase activity, indicating higher SCFV gene expression, was detected in the footpad of macrophage-depleted mice after 24h post infection (hpi). Moreover, FLUC-SCFV particles disseminated to the spleen within 14 hpi in macrophage-depleted, but not control mice. Although macrophages presented SCFV to naïve T cells in vitro, depletion of subcapsular sinus (SCS) macrophages did not alter the magnitude or effector function of the WNV-specific CD8(+) T cell response. Together, these results indicate that SCS macrophages play a role in limiting the dissemination of SCFV early in infection but are not required for the generation of a polyfunctional WNV-specific CD8(+) T cell response in the draining LN.
在节肢动物载体注射后,巨噬细胞会很快遇到黄病毒。通过对感染萤火虫荧光素酶表达的单循环黄病毒颗粒(FLUC-SCFV)的小鼠进行体内成像,我们研究了在存在或不存在淋巴结(LN)驻留巨噬细胞的情况下,病毒颗粒的初始传播情况。在感染后 24 小时(hpi),巨噬细胞耗竭小鼠的足垫中检测到更高的荧光素酶活性,表明更高的 SCFV 基因表达。此外,在巨噬细胞耗竭的小鼠中,FLUC-SCFV 颗粒在 14 hpi 时传播到脾脏,而在对照小鼠中则没有。尽管巨噬细胞在体外将 SCFV 呈递给幼稚 T 细胞,但对被膜下窦(SCS)巨噬细胞的耗竭并未改变 WNV 特异性 CD8(+) T 细胞反应的幅度或效应功能。综上所述,这些结果表明 SCS 巨噬细胞在感染早期限制 SCFV 的传播中发挥作用,但在引流 LN 中产生多功能 WNV 特异性 CD8(+) T 细胞反应时不需要 SCS 巨噬细胞。