流式细胞术循环细胞外囊泡多参数分析预测COVID-19疾病进展

IF 3.8 2区 医学 Q2 VIROLOGY
Evelyn Hammer, Charlotte Flynn, Johannes Rößler, Johanna Erder, Rudolf Napieralski, Lisa Fricke, Birgit Campbell, Martin Feuerherd, Felix Esslinger, Albrecht von Brunn, Timm Weber, Siobhan King, Sisareuth Tan, Alain R Brisson, Ulrike Protzer, Gabriele Schricker, Kathrin Gärtner, Gregor Ebert, Allessandra Moretti, Florian Klein, Kevin Knoops, Ron Heeren, Wolfgang Hammerschmidt, Reinhard Zeidler, Olaf Wilhelm, Percy A Knolle, Bastian Höchst
{"title":"流式细胞术循环细胞外囊泡多参数分析预测COVID-19疾病进展","authors":"Evelyn Hammer, Charlotte Flynn, Johannes Rößler, Johanna Erder, Rudolf Napieralski, Lisa Fricke, Birgit Campbell, Martin Feuerherd, Felix Esslinger, Albrecht von Brunn, Timm Weber, Siobhan King, Sisareuth Tan, Alain R Brisson, Ulrike Protzer, Gabriele Schricker, Kathrin Gärtner, Gregor Ebert, Allessandra Moretti, Florian Klein, Kevin Knoops, Ron Heeren, Wolfgang Hammerschmidt, Reinhard Zeidler, Olaf Wilhelm, Percy A Knolle, Bastian Höchst","doi":"10.1128/jvi.01189-25","DOIUrl":null,"url":null,"abstract":"<p><p>Extracellular vesicles (EVs) are released from all cells of the body. They are considered to mirror the state of the cells from which they are released and circulate in the blood, suggesting a possible use of EV analysis for diagnostic purposes. Here, we report that the analysis of single EVs by flow cytometry can detect infection of cells with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by identifying expression of the SARS-CoV-2 spike (S) protein on the surface of EVs and the cellular origin of EVs by detecting cell-type-specific markers such as troponin (cTNT1) for cardiomyocytes. In coronavirus-associated disease 19 (COVID-19) patients, we detected a direct correlation of the frequencies of circulating S-expressing EVs, but not of cTNT/S-co-expressing EVs, with the subsequent development of a severe disease course. Detection of circulating S-expressing EVs indicates widespread SARS-CoV-2 infection in the body, which may contribute to the immune pathogenesis that triggers tissue and organ damage in COVID-19. Our findings suggest that detecting circulating viral antigen-expressing EVs may provide crucial predictive information on infection-associated disease courses in situations of a future viral pandemic.IMPORTANCEThe ability to predict which patients infected with the SARS-CoV-2 virus will develop severe disease remains a significant clinical challenge. The present study demonstrates that EVs in the peripheral blood, carrying the SARS-CoV-2 spike protein, can be detected by flow cytometry and serve as early biomarkers of disease progression. In contradistinction to PCR or serology, this method provides insight into systemic viral spread and potential organ involvement. The early identification of spike-positive EVs at the time of hospital admission has the potential to facilitate the timely identification of high-risk patients, thereby enhancing the efficacy of triage and subsequent care. This approach may also be of value in terms of facilitating a more rapid and precise response to future virus pandemics.</p>","PeriodicalId":17583,"journal":{"name":"Journal of Virology","volume":" ","pages":"e0118925"},"PeriodicalIF":3.8000,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Prediction of COVID-19 disease progression by multiparametric analysis of circulating extracellular vesicles with flow cytometry.\",\"authors\":\"Evelyn Hammer, Charlotte Flynn, Johannes Rößler, Johanna Erder, Rudolf Napieralski, Lisa Fricke, Birgit Campbell, Martin Feuerherd, Felix Esslinger, Albrecht von Brunn, Timm Weber, Siobhan King, Sisareuth Tan, Alain R Brisson, Ulrike Protzer, Gabriele Schricker, Kathrin Gärtner, Gregor Ebert, Allessandra Moretti, Florian Klein, Kevin Knoops, Ron Heeren, Wolfgang Hammerschmidt, Reinhard Zeidler, Olaf Wilhelm, Percy A Knolle, Bastian Höchst\",\"doi\":\"10.1128/jvi.01189-25\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Extracellular vesicles (EVs) are released from all cells of the body. They are considered to mirror the state of the cells from which they are released and circulate in the blood, suggesting a possible use of EV analysis for diagnostic purposes. Here, we report that the analysis of single EVs by flow cytometry can detect infection of cells with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by identifying expression of the SARS-CoV-2 spike (S) protein on the surface of EVs and the cellular origin of EVs by detecting cell-type-specific markers such as troponin (cTNT1) for cardiomyocytes. In coronavirus-associated disease 19 (COVID-19) patients, we detected a direct correlation of the frequencies of circulating S-expressing EVs, but not of cTNT/S-co-expressing EVs, with the subsequent development of a severe disease course. Detection of circulating S-expressing EVs indicates widespread SARS-CoV-2 infection in the body, which may contribute to the immune pathogenesis that triggers tissue and organ damage in COVID-19. Our findings suggest that detecting circulating viral antigen-expressing EVs may provide crucial predictive information on infection-associated disease courses in situations of a future viral pandemic.IMPORTANCEThe ability to predict which patients infected with the SARS-CoV-2 virus will develop severe disease remains a significant clinical challenge. The present study demonstrates that EVs in the peripheral blood, carrying the SARS-CoV-2 spike protein, can be detected by flow cytometry and serve as early biomarkers of disease progression. In contradistinction to PCR or serology, this method provides insight into systemic viral spread and potential organ involvement. The early identification of spike-positive EVs at the time of hospital admission has the potential to facilitate the timely identification of high-risk patients, thereby enhancing the efficacy of triage and subsequent care. This approach may also be of value in terms of facilitating a more rapid and precise response to future virus pandemics.</p>\",\"PeriodicalId\":17583,\"journal\":{\"name\":\"Journal of Virology\",\"volume\":\" \",\"pages\":\"e0118925\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-09-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Virology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1128/jvi.01189-25\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"VIROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Virology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1128/jvi.01189-25","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"VIROLOGY","Score":null,"Total":0}
引用次数: 0

摘要

细胞外囊泡(EVs)从身体的所有细胞中释放出来。它们被认为反映了它们被释放并在血液中循环的细胞的状态,这表明EV分析可能用于诊断目的。本文报道,流式细胞术分析单个ev可以通过检测ev表面SARS-CoV-2刺突蛋白(S)的表达来检测感染SARS-CoV-2的细胞,并通过检测心肌细胞的肌钙蛋白(cTNT1)等细胞类型特异性标记来检测ev的细胞来源。在冠状病毒相关疾病19 (COVID-19)患者中,我们检测到循环中表达s的ev的频率与随后严重病程的发展直接相关,而不是cTNT/ s共表达ev的频率。检测到循环中表达s的ev表明体内广泛存在SARS-CoV-2感染,这可能有助于引发COVID-19组织和器官损伤的免疫发病机制。我们的研究结果表明,在未来病毒大流行的情况下,检测表达循环病毒抗原的ev可能为感染相关疾病的病程提供重要的预测信息。预测哪些感染了SARS-CoV-2病毒的患者会发展成严重疾病的能力仍然是一项重大的临床挑战。本研究表明,外周血中携带SARS-CoV-2刺突蛋白的ev可以通过流式细胞术检测到,并作为疾病进展的早期生物标志物。与PCR或血清学相比,这种方法提供了对全身病毒传播和潜在器官受累的深入了解。在入院时及早发现尖峰阳性的ev,有可能有助于及时发现高危患者,从而提高分诊和后续护理的效果。这种方法在促进对未来的病毒大流行作出更迅速和准确的反应方面也可能有价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prediction of COVID-19 disease progression by multiparametric analysis of circulating extracellular vesicles with flow cytometry.

Extracellular vesicles (EVs) are released from all cells of the body. They are considered to mirror the state of the cells from which they are released and circulate in the blood, suggesting a possible use of EV analysis for diagnostic purposes. Here, we report that the analysis of single EVs by flow cytometry can detect infection of cells with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by identifying expression of the SARS-CoV-2 spike (S) protein on the surface of EVs and the cellular origin of EVs by detecting cell-type-specific markers such as troponin (cTNT1) for cardiomyocytes. In coronavirus-associated disease 19 (COVID-19) patients, we detected a direct correlation of the frequencies of circulating S-expressing EVs, but not of cTNT/S-co-expressing EVs, with the subsequent development of a severe disease course. Detection of circulating S-expressing EVs indicates widespread SARS-CoV-2 infection in the body, which may contribute to the immune pathogenesis that triggers tissue and organ damage in COVID-19. Our findings suggest that detecting circulating viral antigen-expressing EVs may provide crucial predictive information on infection-associated disease courses in situations of a future viral pandemic.IMPORTANCEThe ability to predict which patients infected with the SARS-CoV-2 virus will develop severe disease remains a significant clinical challenge. The present study demonstrates that EVs in the peripheral blood, carrying the SARS-CoV-2 spike protein, can be detected by flow cytometry and serve as early biomarkers of disease progression. In contradistinction to PCR or serology, this method provides insight into systemic viral spread and potential organ involvement. The early identification of spike-positive EVs at the time of hospital admission has the potential to facilitate the timely identification of high-risk patients, thereby enhancing the efficacy of triage and subsequent care. This approach may also be of value in terms of facilitating a more rapid and precise response to future virus pandemics.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信