O'Brien Benjamin S, Mokry Rebekah L, Schumacher Megan L, Rosas-Rogers Suzette, Terhune Scott S, Ebert Allison D
Department of Cell Biology, Neurobiology, and Anatomy, The Medical College of Wisconsin , Milwaukee, Wisconsin, USA.
Department of Microbiology and Immunology, The Medical College of Wisconsin , Milwaukee, Wisconsin, USA.
J Virol. 2023 Oct 31;97(10):e0069623. doi: 10.1128/jvi.00696-23. Epub 2023 Oct 5.
Human cytomegalovirus (HCMV) infection is the leading cause of non-heritable birth defects worldwide. HCMV readily infects the early progenitor cell population of the developing brain, and we have found that infection leads to significantly downregulated expression of key neurodevelopmental transcripts. Currently, there are no approved therapies to prevent or mitigate the effects of congenital HCMV infection. Therefore, we used human-induced pluripotent stem cell-derived organoids and neural progenitor cells to elucidate the glycoproteins and receptors used in the viral entry process and whether antibody neutralization was sufficient to block viral entry and prevent disruption of neurodevelopmental gene expression. We found that blocking viral entry alone was insufficient to maintain the expression of key neurodevelopmental genes, but neutralization combined with neurotrophic factor treatment provided robust protection. Together, these studies offer novel insight into mechanisms of HCMV infection in neural tissues, which may aid future therapeutic development.
人类巨细胞病毒(HCMV)感染是全球非遗传性出生缺陷的主要原因。HCMV很容易感染发育中大脑的早期祖细胞群体,并且我们发现感染会导致关键神经发育转录本的表达显著下调。目前,尚无获批的疗法来预防或减轻先天性HCMV感染的影响。因此,我们使用人诱导多能干细胞衍生的类器官和神经祖细胞来阐明病毒进入过程中所使用的糖蛋白和受体,以及抗体中和是否足以阻断病毒进入并防止神经发育基因表达受到破坏。我们发现仅阻断病毒进入不足以维持关键神经发育基因的表达,但中和作用与神经营养因子治疗相结合可提供强大的保护作用。总之,这些研究为HCMV在神经组织中的感染机制提供了新的见解,这可能有助于未来的治疗开发。