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不同的炎症特征将 COVID-19 与流感区分开来,细胞因子风暴的贡献有限。

Distinct inflammatory profiles distinguish COVID-19 from influenza with limited contributions from cytokine storm.

机构信息

Department of Emergency Medicine, Washington University School of Medicine, Saint Louis, MO, USA.

Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN, USA.

出版信息

Sci Adv. 2020 Dec 9;6(50). doi: 10.1126/sciadv.abe3024. Print 2020 Dec.

Abstract

We pursued a study of immune responses in coronavirus disease 2019 (COVID-19) and influenza patients. Compared to patients with influenza, patients with COVID-19 exhibited largely equivalent lymphocyte counts, fewer monocytes, and lower surface human leukocyte antigen (HLA)-class II expression on selected monocyte populations. Furthermore, decreased HLA-DR on intermediate monocytes predicted severe COVID-19 disease. In contrast to prevailing assumptions, very few (7 of 168) patients with COVID-19 exhibited cytokine profiles indicative of cytokine storm syndrome. After controlling for multiple factors including age and sample time point, patients with COVID-19 exhibited lower cytokine levels than patients with influenza. Up-regulation of IL-6, G-CSF, IL-1RA, and MCP1 predicted death in patients with COVID-19 but were not statistically higher than patients with influenza. Single-cell transcriptional profiling revealed profound suppression of interferon signaling among patients with COVID-19. When considered across the spectrum of peripheral immune profiles, patients with COVID-19 are less inflamed than patients with influenza.

摘要

我们研究了 2019 冠状病毒病(COVID-19)和流感患者的免疫反应。与流感患者相比,COVID-19 患者的淋巴细胞计数大致相当,单核细胞较少,选定的单核细胞群体表面人白细胞抗原(HLA)-II 类表达水平较低。此外,中间单核细胞 HLA-DR 的降低预示着 COVID-19 疾病的严重程度。与普遍的假设相反,只有少数(168 例中的 7 例)COVID-19 患者表现出细胞因子风暴综合征的细胞因子谱。在控制了年龄和样本时间点等多个因素后,COVID-19 患者的细胞因子水平低于流感患者。IL-6、G-CSF、IL-1RA 和 MCP1 的上调预示着 COVID-19 患者的死亡,但与流感患者相比并没有统计学上的更高。单细胞转录组谱分析显示 COVID-19 患者的干扰素信号受到严重抑制。从外周免疫谱的全谱来看,COVID-19 患者的炎症反应低于流感患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dbe/7725462/aacc112519e4/abe3024-F1.jpg

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