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细胞流行病学——一种在人群层面量化传染病动态的范例。

Celluloepidemiology-A paradigm for quantifying infectious disease dynamics on a population level.

作者信息

Ha My K, Postovskaya Anna, Kuznetsova Maria, Meysman Pieter, Van Deuren Vincent, Van Ierssel Sabrina, De Reu Hans, Schippers Jolien, Peeters Karin, Besbassi Hajar, Heyndrickx Leo, Willems Betty, Mariën Joachim, Bartholomeus Esther, Vercauteren Koen, Beutels Philippe, Van Damme Pierre, Lion Eva, Vlieghe Erika, Laukens Kris, Coenen Samuel, Naesens Reinout, Ariën Kevin K, Ogunjimi Benson

机构信息

Center for Health Economics Research and Modelling Infectious Diseases (CHERMID), Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium.

Antwerp Center for Translational Immunology and Virology (ACTIV), Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium.

出版信息

Sci Adv. 2025 May 16;11(20):eadt2926. doi: 10.1126/sciadv.adt2926.

DOI:10.1126/sciadv.adt2926
PMID:40378227
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12083542/
Abstract

To complement serology as a tool in public health interventions, we introduced the "celluloepidemiology" paradigm where we leveraged pathogen-specific T cell responses at a population level to advance our epidemiological understanding of infectious diseases, using SARS-CoV-2 as a model. Applying flow cytometry and machine learning on data from more than 500 individuals, we showed that the number of T cells with positive expression of functional markers not only could distinguish patients who recovered from COVID-19 from controls and pre-COVID donors but also identify previously unrecognized asymptomatic patients from mild, moderate, and severe recovered patients. The celluloepidemiology approach was uniquely capable to differentiate health care worker groups with different SARS-CoV-2 exposures from each other. T cell receptor (TCR) profiling strengthened our analysis by revealing that SARS-CoV-2-specific TCRs were more abundant in patients than in controls. We believe that adding data on T cell reactivity will complement serology and augment the value of infection morbidity modeling for populations.

摘要

为补充血清学作为公共卫生干预工具的不足,我们引入了“细胞流行病学”范式,即以严重急性呼吸综合征冠状病毒2(SARS-CoV-2)为模型,在人群层面利用病原体特异性T细胞反应来深化我们对传染病的流行病学认识。通过对500多名个体的数据应用流式细胞术和机器学习,我们发现功能性标志物呈阳性表达的T细胞数量不仅可以区分新冠肺炎康复患者与对照组及新冠疫情前的捐赠者,还能从轻症、中症和重症康复患者中识别出此前未被发现的无症状患者。细胞流行病学方法具有独特的能力,能够区分不同SARS-CoV-2暴露程度的医护人员群体。T细胞受体(TCR)分析通过揭示SARS-CoV-2特异性TCR在患者中比在对照组中更丰富,加强了我们的分析。我们认为,增加T细胞反应性数据将补充血清学,并提高人群感染发病率建模的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ab/12083542/f8a587d55d68/sciadv.adt2926-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ab/12083542/9e0db75afbfc/sciadv.adt2926-f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ab/12083542/f8a587d55d68/sciadv.adt2926-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ab/12083542/9e0db75afbfc/sciadv.adt2926-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ab/12083542/d7a9cdd72087/sciadv.adt2926-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ab/12083542/7e31d7f26722/sciadv.adt2926-f3.jpg
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本文引用的文献

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Long COVID manifests with T cell dysregulation, inflammation and an uncoordinated adaptive immune response to SARS-CoV-2.长新冠表现为 T 细胞失调、炎症和对 SARS-CoV-2 的不协调适应性免疫反应。
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Diagnosing Viral Infections Through T-Cell Receptor Sequencing of Activated CD8+ T Cells.
通过激活的 CD8+ T 细胞的 T 细胞受体测序诊断病毒感染。
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