Millennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
Virulence. 2021 Dec;12(1):2583-2607. doi: 10.1080/21505594.2021.1980990.
Herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2) are highly prevalent in the human population. These viruses cause lifelong infections by establishing latency in neurons and undergo sporadic reactivations that promote recurrent disease and new infections. The success of HSVs in persisting in infected individuals is likely due to their multiple molecular determinants involved in escaping the host antiviral and immune responses. Importantly, HSVs infect and negatively modulate the function of dendritic cells (DCs), key immune cells that are involved in establishing effective and balanced immunity against viruses. Here, we review and discuss several molecular and cellular processes modulated by HSVs in DCs, such as autophagy, apoptosis, and the unfolded protein response. Given the central role of DCs in establishing optimal antiviral immunity, particular emphasis should be given to the outcome of the interactions occurring between HSVs and DCs.
单纯疱疹病毒 1 型(HSV-1)和 2 型(HSV-2)在人群中高度流行。这些病毒通过在神经元中建立潜伏感染而导致终身感染,并经历零星的再激活,从而促进疾病复发和新的感染。HSV 能够在感染个体中持续存在,这可能是由于它们涉及多种分子决定因素,这些因素可逃避宿主的抗病毒和免疫反应。重要的是,HSV 感染并负调控树突状细胞(DC)的功能,DC 是参与建立针对病毒的有效和平衡免疫的关键免疫细胞。在这里,我们综述和讨论了 HSV 在 DC 中调节的几种分子和细胞过程,如自噬、细胞凋亡和未折叠蛋白反应。鉴于 DC 在建立最佳抗病毒免疫中的核心作用,应特别重视 HSV 和 DC 之间相互作用的结果。