Department of Surgery, Friedrich-Alexander University (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.
Department of Anesthesiology, Friedrich-Alexander University (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.
Nat Commun. 2021 Feb 18;12(1):1112. doi: 10.1038/s41467-021-21310-4.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a worldwide health threat. In a prospective multicentric study, we identify IL-3 as an independent prognostic marker for the outcome during SARS-CoV-2 infections. Specifically, low plasma IL-3 levels is associated with increased severity, viral load, and mortality during SARS-CoV-2 infections. Patients with severe COVID-19 exhibit also reduced circulating plasmacytoid dendritic cells (pDCs) and low plasma IFNα and IFNλ levels when compared to non-severe COVID-19 patients. In a mouse model of pulmonary HSV-1 infection, treatment with recombinant IL-3 reduces viral load and mortality. Mechanistically, IL-3 increases innate antiviral immunity by promoting the recruitment of circulating pDCs into the airways by stimulating CXCL12 secretion from pulmonary CD123 epithelial cells, both, in mice and in COVID-19 negative patients exhibiting pulmonary diseases. This study identifies IL-3 as a predictive disease marker for SARS-CoV-2 infections and as a potential therapeutic target for pulmunory viral infections.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)是全球健康威胁。在一项前瞻性多中心研究中,我们发现白细胞介素 3(IL-3)是 SARS-CoV-2 感染结局的独立预后标志物。具体而言,低血浆 IL-3 水平与 SARS-CoV-2 感染期间的严重程度增加、病毒载量增加和死亡率增加相关。与非重症 COVID-19 患者相比,重症 COVID-19 患者还表现出循环浆细胞样树突状细胞(pDC)减少和血浆 IFNα 和 IFNλ 水平降低。在肺单纯疱疹病毒 1 感染的小鼠模型中,用重组 IL-3 治疗可降低病毒载量和死亡率。其机制为,IL-3 通过刺激肺 CD123 上皮细胞分泌趋化因子(C-X-C 基序)配体 12(CXCL12),促进循环 pDC 向气道募集,从而增强先天抗病毒免疫,这在小鼠和患有肺部疾病的 COVID-19 阴性患者中均有体现。本研究将 IL-3 鉴定为 SARS-CoV-2 感染的预测疾病标志物和肺部病毒感染的潜在治疗靶点。