Department of Microbiology and Immunology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Department of Microbiology and Immunology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA
mSphere. 2019 Mar 27;4(2):e00073-19. doi: 10.1128/mSphere.00073-19.
Sex differences related to immune response and inflammation play a role in the susceptibility and pathogenesis of a variety of viral infections and disease (S. L. Klein, Bioessays 34:1050-1059, 2012, https://doi.org/10.1002/bies.201200099). Herpes simplex virus 1 (HSV-1) causes chronic inflammatory disease in the cornea, an immune-privileged tissue, resulting in irreversible damage and blindness in affected individuals (A. Rowe, A. St Leger, S. Jeon, D. K. Dhaliwal, et al., Prog Retin Eye Res 32:88-101, 2013, https://doi.org/10.1016/j.preteyeres.2012.08.002). Our research focuses on the role of herpesvirus entry mediator (HVEM) as an immune regulator during ocular HSV-1 infection. Mice lacking HVEM (HVEM knockout [KO] mice) exhibit lower levels of immune cell infiltrates and less severe ocular disease in the cornea than wild-type (WT) mice. As sex differences contribute to pathogenesis in many inflammatory diseases, we tested whether sex acts as a biological variable in the immune response to HSV-1 infection and herpes stromal keratitis (HSK) pathogenesis. Adult male and female WT and HVEM KO mice were inoculated with HSV-1 via corneal scarification and monitored daily for disease course. Viral titers were determined, and immune cell infiltrates were collected and analyzed. Our results indicated no significant differences in viral titers in tear film or affected tissues, in immune cell infiltration, or in clinical symptoms between males and females of either genotype. These results suggest that sex is not a significant biological variable in this experimental model and that male and female mice of the C57BL/6 background can be used similarly in studies of ocular HSV-1 pathogenesis. Sex hormones have come to be considered an important factor for the development of certain diseases only recently and as such should continue to be considered a biological variable. Ocular HSV-1, and the resulting HSK, is the leading cause of infectious blindness worldwide. We compared levels of ocular HSV-1 infection and pathogenesis in the two sexes and found no significance differences between male and female WT mice or HVEM KO mice.
性别的差异与免疫反应和炎症有关,在各种病毒感染和疾病的易感性和发病机制中起着作用(S.L. Klein,Bioessays 34:1050-1059,2012,https://doi.org/10.1002/bies.201200099)。单纯疱疹病毒 1(HSV-1)在免疫特权组织角膜中引起慢性炎症性疾病,导致受影响个体的不可逆损伤和失明(A. Rowe、A. St Leger、S. Jeon、D.K. Dhaliwal 等人,Prog Retin Eye Res 32:88-101,2013,https://doi.org/10.1016/j.preteyeres.2012.08.002)。我们的研究重点是疱疹病毒进入介体(HVEM)在眼部单纯疱疹病毒 1 感染期间作为免疫调节剂的作用。缺乏 HVEM(HVEM 敲除 [KO] 小鼠)的小鼠在角膜中显示出较低水平的免疫细胞浸润和较轻的眼部疾病,而野生型(WT)小鼠则没有。由于性别差异会导致许多炎症性疾病的发病机制,因此我们测试了性别是否是对 HSV-1 感染和疱疹性基质性角膜炎(HSK)发病机制的免疫反应的生物学变量。成年雄性和雌性 WT 和 HVEM KO 小鼠通过角膜划痕接种 HSV-1,并每天监测疾病过程。测定病毒滴度,并收集和分析免疫细胞浸润。我们的结果表明,在泪膜或受影响组织中的病毒滴度、免疫细胞浸润或临床症状方面,两种基因型的雄性和雌性之间没有显着差异。这些结果表明,在这种实验模型中,性别不是一个重要的生物学变量,并且 C57BL/6 背景的雄性和雌性小鼠可以在眼部单纯疱疹病毒 1 发病机制的研究中类似地使用。性激素最近才被认为是某些疾病发展的重要因素,因此应继续被视为生物学变量。眼部单纯疱疹病毒 1 和由此产生的 HSK 是全球感染性失明的主要原因。我们比较了两性的眼部单纯疱疹病毒 1 感染和发病机制水平,在 WT 小鼠或 HVEM KO 小鼠的雄性和雌性之间没有发现显着差异。