Martínez-Espinoza Iván, Guerrero-Plata Antonieta
Department of Pathobiological Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803, USA.
Pathogens. 2025 Jul 14;14(7):694. doi: 10.3390/pathogens14070694.
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.
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。