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High-dimensional single-cell analysis reveals the immune characteristics of COVID-19

机译:高尺寸单细胞分析显示Covid-19的免疫特征

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摘要

Coronavirus disease 2019 (COVID-19), driven by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), was declared a global pandemic in March 2020. Pathogenic T cells and inflammatory monocytes are regarded as the central drivers of the cyto-kine storm associated with the severity of COVID-19. In this study, we explored the characteristic peripheral cellular profiles of patients with COVID-19 in both acute and convalescent phases by single-cell mass cytometry (CyTOF). Using a combination of algorithm-guided data analyses, we identified peripheral immune cell subsets in COVID-19 and revealed CD4+ T-cell depletion, T-cell differentiation, plasma cell expansion, and the reduced antigen presentation capacity of innate immunity. Notably, COVID-19 induces a dysregulation in the balance of monocyte populations by the expansion of the monocyte subsets. Collectively, our results represent a high-dimensional, single-cell profile of the peripheral immune response to SARS-CoV-2 infection.
机译:由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引发的2019年冠状病毒病(COVID-19)于2020年3月被宣布为全球大流行。2019冠状病毒疾病和炎症性单核细胞被认为是Cyto-KeV的主要驱动因素。在2019冠状病毒疾病患者中,我们采用单细胞质量流术(CytoCo)检测了COVID-19患者急性期和恢复期的外周血细胞特征。2019冠状病毒疾病的免疫组化结果表明,CD4+T细胞耗竭、T细胞分化、浆细胞扩增和固有免疫抗原表达能力降低。值得注意的是,COVID-19诱导单核细胞群体的平衡失调单核细胞亚群的扩展。总的来说,我们的结果代表了对SARS-CoV-2感染的外周免疫反应的高维单细胞特征。

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