Center for Neurobiology and Vaccine Development, Ophthalmology Research, Department of Surgery, Cedars-Sinai Burns & Allen Research Institute, CSMC-SSB3, Los Angeles, CA, United States of America.
PLoS One. 2019 Apr 18;14(4):e0215727. doi: 10.1371/journal.pone.0215727. eCollection 2019.
Complex interactions between HSV-1 and infiltrating immune cells play important roles in establishing localized, acute virus replication as well as chronic latent infection. The extent and duration of initial virus replication are the key determinants of subsequent pathologic inflammatory responses and therefore, the accumulation of immune cell populations at this time point is a key target for prevention. Therefore, we evaluated the role of various immune cell infiltrates between 1 h and 28 days post-infection (PI) using mice infected with virulent HSV-1 strain McKrae without corneal scarification. The effect of corneal scarification on immune cell infiltrates was also determined. We first determined the activation status and origin of macrophage infiltrates as early as 1 h PI. We found a sharp increase in the total macrophage population after 12 h PI, that was primarily due to infiltration of CCR2+ migratory macrophages, mostly in M1 status (MHC II+). The number of CCR2- resident macrophages, mostly unpolarized (M0), increased gradually over time and peaked at 48 h PI. Interestingly, some of the resident macrophages gained an M2-like phenotype (CD206Low), which peaked at 12 h PI, concurrent with M1 macrophage infiltration. From 1-7 days PI, infiltration of various immune cells correlated strongly with HSV-1 replication, with neutrophils showing the biggest increase, and NKT cells the biggest decrease, after infection. The presence of geographical ulcer did not correlate with increased infiltration, while mice with corneal scarring had significantly more immune cell infiltration than those without corneal scarring. Overall, we showed time-dependent infiltration of various immune cells in the eye of HSV-1 infected mice. Initial infiltration of macrophages followed by infiltration of T cells at later times PI demonstrates the importance of targeting macrophages rather than other immune cells type, for therapeutic treatment of HSV-1.
单纯疱疹病毒 1 与浸润免疫细胞之间的复杂相互作用在建立局部、急性病毒复制以及慢性潜伏感染方面发挥着重要作用。初始病毒复制的程度和持续时间是随后病理炎症反应的关键决定因素,因此,此时点免疫细胞群体的积累是预防的关键目标。因此,我们使用未进行角膜划痕的、感染了强毒力 HSV-1 株 McKrae 的小鼠,评估了 1 小时至 28 天感染后(PI)各种免疫细胞浸润的作用。还确定了角膜划痕对免疫细胞浸润的影响。我们首先在 1 h PI 时确定了巨噬细胞浸润的激活状态和来源。我们发现,在 12 h PI 后,总巨噬细胞群体急剧增加,这主要是由于 CCR2+迁移巨噬细胞的浸润,主要处于 M1 状态(MHC II+)。CCR2-驻留巨噬细胞的数量逐渐增加,时间上逐渐增加,并在 48 h PI 时达到峰值。有趣的是,一些驻留巨噬细胞获得了 M2 样表型(CD206Low),在 12 h PI 时达到峰值,与 M1 巨噬细胞浸润同时发生。在 1-7 天 PI 期间,各种免疫细胞的浸润与 HSV-1 复制密切相关,感染后中性粒细胞的增加最大,NKT 细胞的减少最大。地理溃疡的存在与浸润增加无关,而角膜划痕的小鼠比没有角膜划痕的小鼠有明显更多的免疫细胞浸润。总体而言,我们显示了 HSV-1 感染小鼠眼睛中各种免疫细胞的时间依赖性浸润。巨噬细胞的初始浸润随后是在较晚的时间点 PI 时的 T 细胞浸润,这表明针对巨噬细胞而不是其他免疫细胞类型进行治疗性治疗 HSV-1 的重要性。