Whole blood immunophenotyping uncovers immature neutrophil-to-VD2 T-cell ratio as an early marker for severe COVID-19
SARS-CoV-2 is the novel coronavirus responsible for the current COVID-19 pandemic. Severe complications are observed only in a small proportion of infected patients but the cellular mechanisms underlying this progression are still unknown. Comprehensive flow cytometry of whole blood samples from 54...
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Published in | Nature communications Vol. 11; no. 1; p. 5243 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , |
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Nature Publishing Group UK
16.10.2020
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Abstract | SARS-CoV-2 is the novel coronavirus responsible for the current COVID-19 pandemic. Severe complications are observed only in a small proportion of infected patients but the cellular mechanisms underlying this progression are still unknown. Comprehensive flow cytometry of whole blood samples from 54 COVID-19 patients reveals a dramatic increase in the number of immature neutrophils. This increase strongly correlates with disease severity and is associated with elevated IL-6 and IP-10 levels, two key players in the cytokine storm. The most pronounced decrease in cell counts is observed for CD8 T-cells and VD2 γδ T-cells, which both exhibit increased differentiation and activation. ROC analysis reveals that the count ratio of immature neutrophils to VD2 (or CD8) T-cells predicts pneumonia onset (0.9071) as well as hypoxia onset (0.8908) with high sensitivity and specificity. It would thus be a useful prognostic marker for preventive patient management and improved healthcare resource management.
COVID-19 severity is associated with cytokine levels and lymphopenia, but the role of immune cell subsets is not well understood. Here the authors immunophenotype whole blood samples from 54 COVID-19 patients and find that the immature neutrophil-to-VD2 T-cell ratio is associated with severe COVID-19. |
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AbstractList | COVID-19 severity is associated with cytokine levels and lymphopenia, but the role of immune cell subsets is not well understood. Here the authors immunophenotype whole blood samples from 54 COVID-19 patients and find that the immature neutrophil-to-VD2 T-cell ratio is associated with severe COVID-19. SARS-CoV-2 is the novel coronavirus responsible for the current COVID-19 pandemic. Severe complications are observed only in a small proportion of infected patients but the cellular mechanisms underlying this progression are still unknown. Comprehensive flow cytometry of whole blood samples from 54 COVID-19 patients reveals a dramatic increase in the number of immature neutrophils. This increase strongly correlates with disease severity and is associated with elevated IL-6 and IP-10 levels, two key players in the cytokine storm. The most pronounced decrease in cell counts is observed for CD8 T-cells and VD2 γδ T-cells, which both exhibit increased differentiation and activation. ROC analysis reveals that the count ratio of immature neutrophils to VD2 (or CD8) T-cells predicts pneumonia onset (0.9071) as well as hypoxia onset (0.8908) with high sensitivity and specificity. It would thus be a useful prognostic marker for preventive patient management and improved healthcare resource management. COVID-19 severity is associated with cytokine levels and lymphopenia, but the role of immune cell subsets is not well understood. Here the authors immunophenotype whole blood samples from 54 COVID-19 patients and find that the immature neutrophil-to-VD2 T-cell ratio is associated with severe COVID-19. SARS-CoV-2 is the novel coronavirus responsible for the current COVID-19 pandemic. Severe complications are observed only in a small proportion of infected patients but the cellular mechanisms underlying this progression are still unknown. Comprehensive flow cytometry of whole blood samples from 54 COVID-19 patients reveals a dramatic increase in the number of immature neutrophils. This increase strongly correlates with disease severity and is associated with elevated IL-6 and IP-10 levels, two key players in the cytokine storm. The most pronounced decrease in cell counts is observed for CD8 T-cells and VD2 γδ T-cells, which both exhibit increased differentiation and activation. ROC analysis reveals that the count ratio of immature neutrophils to VD2 (or CD8) T-cells predicts pneumonia onset (0.9071) as well as hypoxia onset (0.8908) with high sensitivity and specificity. It would thus be a useful prognostic marker for preventive patient management and improved healthcare resource management. |
ArticleNumber | 5243 |
Author | Larbi, Anis Chan, Yi-Hao Amrun, Siti Naqiah Andiappan, Anand Kumar Fan, Bingwen Eugene Ng, Lai Guan Lee, Bernett Rötzschke, Olaf Abdad, Mohammad Yazid Puan, Kia Joo Young, Barnaby Edward Xu, Weili Renia, Laurent Yeo, Nicholas Kim-Wah Kwok, Immanuel Fong, Siew-Wai Lye, David Chien How, Wilson Chan, Stephrene Ng, Lisa FP Carissimo, Guillaume Leo, Yee-Sin Lee, Cheryl Yi-Pin Chee, Rhonda Sin-Ling |
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and Research, Immunos – sequence: 13 givenname: Stephrene surname: Chan fullname: Chan, Stephrene organization: Department of Haematology, Tan Tock Seng Hospital, Department of Laboratory Medicine, Khoo Teck Puat Hospital, Lee Kong Chian School of Medicine, Yong Loo Lin School of Medicine – sequence: 14 givenname: Bingwen Eugene orcidid: 0000-0003-4367-5182 surname: Fan fullname: Fan, Bingwen Eugene organization: Department of Haematology, Tan Tock Seng Hospital, Department of Laboratory Medicine, Khoo Teck Puat Hospital, Lee Kong Chian School of Medicine, Yong Loo Lin School of Medicine – sequence: 15 givenname: Anand Kumar orcidid: 0000-0002-8442-1544 surname: Andiappan fullname: Andiappan, Anand Kumar organization: Singapore Immunology Network, Agency for Science, Technology and Research, Immunos – sequence: 16 givenname: Bernett surname: Lee fullname: Lee, Bernett organization: Singapore Immunology Network, Agency for Science, Technology and Research, Immunos – sequence: 17 givenname: Olaf surname: Rötzschke fullname: Rötzschke, Olaf organization: Singapore Immunology Network, Agency for Science, Technology and Research, Immunos – sequence: 18 givenname: Barnaby Edward orcidid: 0000-0003-1010-2230 surname: Young fullname: Young, Barnaby Edward organization: National Centre for Infectious Diseases, Department of Infectious Diseases, Tan Tock Seng Hospital, Lee Kong Chian School of Medicine, Nanyang Technological University – sequence: 19 givenname: Yee-Sin orcidid: 0000-0003-4978-5825 surname: Leo fullname: Leo, Yee-Sin organization: National Centre for Infectious Diseases, Department of Infectious Diseases, Tan Tock Seng Hospital, Lee Kong Chian School of Medicine, Nanyang Technological University, Yong Loo Lin School of Medicine, National University of Singapore and National University Health System, Saw Swee Hock School of Public Health, National University Singapore – sequence: 20 givenname: David Chien surname: Lye fullname: Lye, David Chien organization: National Centre for Infectious Diseases, Department of Infectious Diseases, Tan Tock Seng Hospital, Lee Kong Chian School of Medicine, Nanyang Technological University, Yong Loo Lin School of Medicine, National University of Singapore and National University Health System – sequence: 21 givenname: Laurent orcidid: 0000-0003-0349-1557 surname: Renia fullname: Renia, Laurent organization: Infectious Disease Horizontal Technology Center, Agency for Science, Technology and Research, Immunos, Singapore Immunology Network, Agency for Science, Technology and Research, Immunos – sequence: 22 givenname: Lai Guan orcidid: 0000-0003-1905-3586 surname: Ng fullname: Ng, Lai Guan organization: Singapore Immunology Network, Agency for Science, Technology and Research, Immunos – sequence: 23 givenname: Anis surname: Larbi fullname: Larbi, Anis organization: Singapore Immunology Network, Agency for Science, Technology and Research, Immunos – sequence: 24 givenname: Lisa FP orcidid: 0000-0003-4071-5222 surname: Ng fullname: Ng, Lisa FP email: lisa_ng@immunol.a-star.edu.sg organization: Infectious Disease Horizontal Technology Center, Agency for Science, Technology and Research, Immunos, Singapore Immunology Network, Agency for Science, Technology and Research, Immunos, Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool |
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Snippet | SARS-CoV-2 is the novel coronavirus responsible for the current COVID-19 pandemic. Severe complications are observed only in a small proportion of infected... COVID-19 severity is associated with cytokine levels and lymphopenia, but the role of immune cell subsets is not well understood. Here the authors... |
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SubjectTerms | 13/21 13/31 631/250/127 631/250/2520 631/250/255 631/326/596/4130 Betacoronavirus - immunology Biomarkers - blood CD8-Positive T-Lymphocytes - immunology Coronavirus Infections - immunology Coronavirus Infections - pathology COVID-19 Cytokine Release Syndrome - immunology Cytokine Release Syndrome - pathology Flow Cytometry Humanities and Social Sciences Humans Immunophenotyping - methods Interleukin-10 - blood Interleukin-6 - blood Lymphocyte Count multidisciplinary Neutrophils - immunology Pandemics Pneumonia, Viral - immunology Pneumonia, Viral - pathology Receptors, Antigen, T-Cell, gamma-delta - immunology SARS-CoV-2 Science Science (multidisciplinary) Severity of Illness Index |
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Title | Whole blood immunophenotyping uncovers immature neutrophil-to-VD2 T-cell ratio as an early marker for severe COVID-19 |
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