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人偏肺病毒和呼吸道合胞病毒在巨噬细胞中诱导的干扰素和促炎细胞因子的相反反应

Opposite Responses of Interferon and Proinflammatory Cytokines Induced by Human Metapneumovirus and Respiratory Syncytial Virus in Macrophages.

作者信息

Martínez-Espinoza Iván, Guerrero-Plata Antonieta

机构信息

Department of Pathobiological Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803, USA.

出版信息

Pathogens. 2025 Jul 14;14(7):694. doi: 10.3390/pathogens14070694.

Abstract

Macrophages are a principal pulmonary source of type I and III interferons (IFNs), initiating and coordinating the early antiviral response to respiratory viral infections. Yet the contribution of macrophage-derived IFNs to host defense during human metapneumovirus (HMPV) infection remains poorly defined. Here, we use human primary monocyte-derived macrophages (MDMs) and THP-1-derived macrophages to analyze the IFN responses induced by HMPV compared to its closely related human pneumovirus, respiratory syncytial virus (RSV). We show that HMPV induced a robust response of type I and type III IFNs and ISGs, whereas RSV elicited only a modest, delayed IFN response despite strong IRF activation; instead, RSV preferentially activates NF-κB and exhibits a pronounced proinflammatory cytokine output. Our results highlight the role of macrophages as key modulators of the IFN and proinflammatory responses during HMPV and RSV infection.

摘要

巨噬细胞是I型和III型干扰素(IFN)的主要肺部来源,启动并协调对呼吸道病毒感染的早期抗病毒反应。然而,在人偏肺病毒(HMPV)感染期间,巨噬细胞衍生的IFN对宿主防御的贡献仍不清楚。在这里,我们使用人原代单核细胞衍生的巨噬细胞(MDM)和THP-1衍生的巨噬细胞来分析HMPV与其密切相关的人肺病毒呼吸道合胞病毒(RSV)相比所诱导的IFN反应。我们发现,HMPV诱导了I型和III型IFN以及ISG的强烈反应,而RSV尽管有强烈的IRF激活,但仅引发了适度的、延迟的IFN反应;相反,RSV优先激活NF-κB并表现出明显的促炎细胞因子输出。我们的结果突出了巨噬细胞在HMPV和RSV感染期间作为IFN和促炎反应关键调节因子的作用。

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