Department of Microbiology, Faculty of Medicine, Kindai University, 377-2 Ohnohigashi, Osakasayama, Osaka 589-8511, Japan.
Department of Arts and Sciences, Faculty of Medicine, Kindai University, Osaka 589-8511, Japan.
Int J Mol Sci. 2024 Mar 19;25(6):3460. doi: 10.3390/ijms25063460.
Theiler's murine encephalomyelitis virus (TMEV) infection has been used as a mouse model for two virus-induced organ-specific immune-mediated diseases. TMEV-induced demyelinating disease (TMEV-IDD) in the central nervous system (CNS) is a chronic inflammatory disease with viral persistence and an animal model of multiple sclerosis (MS) in humans. TMEV infection can also cause acute myocarditis with viral replication and immune cell infiltration in the heart, leading to cardiac fibrosis. Since platelets have been reported to modulate immune responses, we aimed to determine the role of platelets in TMEV infection. In transcriptome analyses of platelets, distinct sets of immune-related genes, including major histocompatibility complex (MHC) class I, were up- or downregulated in TMEV-infected mice at different time points. We depleted platelets from TMEV-infected mice by injecting them with platelet-specific antibodies. The platelet-depleted mice had significantly fewer viral antigen-positive cells in the CNS. Platelet depletion reduced the severities of TMEV-IDD and myocarditis, although the pathology scores did not reach statistical significance. Immunologically, the platelet-depleted mice had an increase in interferon (IFN)-γ production with a higher anti-TMEV IgG2a/IgG1 ratio. Thus, platelets may play roles in TMEV infection, such as gene expression, viral clearance, and anti-viral antibody isotype responses.
Theiler 氏鼠脑脊髓炎病毒(TMEV)感染已被用作两种病毒诱导的器官特异性免疫介导疾病的小鼠模型。中枢神经系统(CNS)中的 TMEV 诱导脱髓鞘病(TMEV-IDD)是一种慢性炎症性疾病,具有病毒持续性,是人类多发性硬化症(MS)的动物模型。TMEV 感染也可导致急性心肌炎,病毒在心脏中复制并伴有免疫细胞浸润,导致心脏纤维化。由于已有报道称血小板可调节免疫反应,因此我们旨在确定血小板在 TMEV 感染中的作用。在血小板的转录组分析中,在不同时间点感染 TMEV 的小鼠中,一组独特的免疫相关基因(包括主要组织相容性复合体(MHC)I 类)被上调或下调。我们通过注射血小板特异性抗体从 TMEV 感染的小鼠中耗尽血小板。血小板耗竭的小鼠中枢神经系统中病毒抗原阳性细胞明显减少。尽管病理评分没有达到统计学意义,但血小板耗竭可降低 TMEV-IDD 和心肌炎的严重程度。免疫方面,血小板耗竭的小鼠 IFN-γ 产生增加,抗 TMEV IgG2a/IgG1 比值升高。因此,血小板可能在 TMEV 感染中发挥作用,例如基因表达、病毒清除和抗病毒抗体同种型反应。