Department of Pediatric Infectious Disease, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang Province 325027, China.
Department of Emergency, Children's Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.
J Immunol Res. 2023 May 12;2023:1462048. doi: 10.1155/2023/1462048. eCollection 2023.
Human cytomegalovirus (HCMV) infection is globally distributed, and the liver is one of the major targeting organs. So far, the mechanisms for cell and organ damage have not fully been elucidated and the treatments for the infection are mainly at symptoms. IL-37 has shown a protective role in certain inflammatory diseases. In the present study, potential protective effect of exogenous IL-37 on murine cytomegalovirus- (MCMV-) infected hepatitis was evaluated through analyses of serum transaminases, the liver histopathology and cytokine expression, and functional state of dendritic cells (DCs) and regulatory T cells (Tregs). These analyses showed a significant decrease in serum transaminase levels and a lower Ishak histopathologic score at the early stage of MCMV-infected mice with exogenous IL-37 pretreatment. The frequencies of MHC-Ⅱ, CD40, CD80, and CD86 positive DCs in the liver and spleen were decreased significantly at 7 days postinfection (dpi) in MCMV-infected mice with IL-37 pretreatment when compared with those without the pretreatment, while the total number of DCs in the liver was reduced in IL-37-pretreated mice. The induction of Tregs in the spleen was enhanced at dpi 3 with IL-37 pretreatment in MCMV-infected mice. The mRNA expression levels of cytokines in the liver were decreased significantly (IL-1, IL-6, IL-10, IL-4) or to some extent (TGF- and TNF-). The present study suggested that exogenous IL-37 can alleviate MCMV-infected hepatitis, likely through reduced DCs and induced Tregs with a weaker cytokine storm, demonstrating its potential value in clinical management for HCMV-infected hepatitis.
人巨细胞病毒(HCMV)感染在全球范围内分布,肝脏是主要的靶器官之一。迄今为止,细胞和器官损伤的机制尚未完全阐明,感染的治疗主要针对症状。IL-37 在某些炎症性疾病中表现出保护作用。在本研究中,通过分析血清转氨酶、肝组织病理学和细胞因子表达以及树突状细胞(DCs)和调节性 T 细胞(Tregs)的功能状态,评估了外源性 IL-37 对鼠巨细胞病毒(MCMV)感染性肝炎的潜在保护作用。这些分析表明,在 MCMV 感染的小鼠中,外源性 IL-37 预处理可显著降低血清转氨酶水平和伊沙克组织病理学评分。与未预处理的 MCMV 感染小鼠相比,IL-37 预处理的 MCMV 感染小鼠在感染后 7 天(dpi)时,肝和脾中 MHC-Ⅱ、CD40、CD80 和 CD86 阳性 DC 的频率显著降低,而肝中 DC 的总数在 IL-37 预处理的小鼠中减少。在 MCMV 感染的小鼠中,IL-37 预处理可增强脾中 Treg 的诱导。在 MCMV 感染的小鼠中,IL-37 预处理可显著降低(IL-1、IL-6、IL-10、IL-4)或在一定程度上降低(TGF-和 TNF-)肝脏中细胞因子的 mRNA 表达水平。本研究表明,外源性 IL-37 可缓解 MCMV 感染性肝炎,可能通过减少 DCs 和诱导较弱细胞因子风暴的 Tregs 来发挥作用,这表明其在 HCMV 感染性肝炎的临床管理中有潜在价值。