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Immunomodulatory and antiviral effects of Lycium barbarum glycopeptide on influenza a virus infection

病毒性肺炎 体内 病毒 免疫系统 肺炎 甲型流感病毒 生物 微生物学 免疫学 炎症 病毒学 医学 传染病(医学专业) 生物技术 病理 内科学 疾病 2019年冠状病毒病(COVID-19)
作者
Runwei Li,Shuang Qu,Meng Qin,Lu Huang,Yi‐Chun Huang,Yi Du,Zhexiong Yu,Fu Fan,Jing Sun,Qiushuang Li,Kwok‐Fai So
出处
期刊:Microbial Pathogenesis [Elsevier]
卷期号:176: 106030-106030 被引量:24
标识
DOI:10.1016/j.micpath.2023.106030
摘要

Influenza is caused by a respiratory virus and has a major global impact on human health. Influenza A viruses in particular are highly pathogenic to humans and have caused multiple pandemics. An important consequence of infection is viral pneumonia, and with serious complications of excessive inflammation and tissue damage. Therefore, simultaneously reducing direct damage caused by virus infection and relieving indirect damage caused by excessive inflammation would be an effective treatment strategy. Lycium barbarum glycopeptide (LbGp) is a mixture of five highly branched polysaccharide-protein conjuncts (LbGp1-5) isolated from Lycium barbarum fruit. LbGp has pro-immune activity that is 1-2 orders of magnitude stronger than that of other plant polysaccharides. However, there are few reports on the immunomodulatory and antiviral activities of LbGp. In this study, we evaluated the antiviral and immunomodulatory effects of LbGp in vivo and in vitro and investigated its therapeutic effect on H1N1-induced viral pneumonia and mechanisms of action. In vitro, cytokine secretion, NF-κB p65 nuclear translocation, and CD86 mRNA expression in LPS-stimulated RAW264.7 cells were constrained by LbGp treatment. In A549 cells, LbGp can inhibit H1N1 infection by blocking virus attachment and entry action. In vivo experiments confirmed that administration of LbGp can effectively increase the survival rate, body weight and decrease the lung index of mice infected with H1N1. Compared to the model group, pulmonary histopathologic symptoms in lung sections of mice treated with LbGp were obviously alleviated. Further investigation revealed that the mechanism of LbGp in the treatment of H1N1-induced viral pneumonia includes reducing the viral load in lung, regulating the phenotype of pulmonary macrophages, and inhibiting excessive inflammation. In conclusion, LbGp exhibits potential curative effects against H1N1-induced viral pneumonia in mice, and these effects are associated with its good immuno-regulatory and antiviral activities.
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