Convalescent COVID-19 Patients Without Comorbidities Display Similar Immunophenotypes Over Time Despite Divergent Disease Severities

COVID-19, the disease caused by SARS-CoV-2 infection, can assume a highly variable disease course, ranging from asymptomatic infection, which constitutes the majority of cases, to severe respiratory failure. This implies a diverse host immune response to SARS-CoV-2. However, the immunological underp...

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Main Authors: Chang-Feng Chu, Florian Sabath, Silvia Fibi-Smetana, Shan Sun, Rupert Öllinger, Elfriede Noeßner, Ying-Yin Chao, Linus Rinke, Elena Winheim, Roland Rad, Anne B. Krug, Leila Taher, Christina E. Zielinski
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-08-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2021.601080/full
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spelling doaj-a4a5a8a224bb40909430cdabe11e93022021-08-19T14:31:31ZengFrontiers Media S.A.Frontiers in Immunology1664-32242021-08-011210.3389/fimmu.2021.601080601080Convalescent COVID-19 Patients Without Comorbidities Display Similar Immunophenotypes Over Time Despite Divergent Disease SeveritiesChang-Feng Chu0Chang-Feng Chu1Chang-Feng Chu2Florian Sabath3Silvia Fibi-Smetana4Shan Sun5Shan Sun6Rupert Öllinger7Elfriede Noeßner8Ying-Yin Chao9Ying-Yin Chao10Linus Rinke11Elena Winheim12Roland Rad13Anne B. Krug14Leila Taher15Christina E. Zielinski16Christina E. Zielinski17Christina E. Zielinski18Institute of Virology, Technical University of Munich, Munich, GermanyCentral Institute for Translational Cancer Research (TranslaTUM), Technical University of Munich, Munich, GermanyInfection Immunology, Leibniz Institute for Natural Product Research and Infection Biology, Hans-Knöll-Institute, Friedrich Schiller University, Jena, GermanyCentral Institute for Translational Cancer Research (TranslaTUM), Technical University of Munich, Munich, GermanyInstitute of Biomedical Informatics, Graz University of Technology, Graz, AustriaInstitute of Virology, Technical University of Munich, Munich, GermanyCentral Institute for Translational Cancer Research (TranslaTUM), Technical University of Munich, Munich, GermanyCentral Institute for Translational Cancer Research (TranslaTUM), Technical University of Munich, Munich, GermanyImmunoanalytics-Tissue Control of Immunocytes, Helmholtz Zentrum München, German Research Center for Environmental Health, Munich, GermanyInstitute of Virology, Technical University of Munich, Munich, GermanyCentral Institute for Translational Cancer Research (TranslaTUM), Technical University of Munich, Munich, GermanyInstitute for Immunology, Biomedical Center, Faculty of Medicine, Ludwig-Maximilians-University Munich, Planegg-Martinsried, GermanyInstitute for Immunology, Biomedical Center, Faculty of Medicine, Ludwig-Maximilians-University Munich, Planegg-Martinsried, GermanyCentral Institute for Translational Cancer Research (TranslaTUM), Technical University of Munich, Munich, GermanyInstitute for Immunology, Biomedical Center, Faculty of Medicine, Ludwig-Maximilians-University Munich, Planegg-Martinsried, GermanyInstitute of Biomedical Informatics, Graz University of Technology, Graz, AustriaInstitute of Virology, Technical University of Munich, Munich, GermanyCentral Institute for Translational Cancer Research (TranslaTUM), Technical University of Munich, Munich, GermanyInfection Immunology, Leibniz Institute for Natural Product Research and Infection Biology, Hans-Knöll-Institute, Friedrich Schiller University, Jena, GermanyCOVID-19, the disease caused by SARS-CoV-2 infection, can assume a highly variable disease course, ranging from asymptomatic infection, which constitutes the majority of cases, to severe respiratory failure. This implies a diverse host immune response to SARS-CoV-2. However, the immunological underpinnings underlying these divergent disease courses remain elusive. We therefore set out to longitudinally characterize immune signatures of convalescent COVID-19 patients stratified according to their disease severity. Our unique convalescent COVID-19 cohort consists of 74 patients not confounded by comorbidities. This is the first study of which we are aware that excludes immune abrogations associated with non-SARS-CoV-2 related risk factors of disease severity. Patients were followed up and analyzed longitudinally (2, 4 and 6 weeks after infection) by high-dimensional flow cytometric profiling of peripheral blood mononuclear cells (PBMCs), in-depth serum analytics, and transcriptomics. Immune phenotypes were correlated to disease severity. Convalescence was overall associated with uniform immune signatures, but distinct immune signatures for mildly versus severely affected patients were detectable within a 2-week time window after infection.https://www.frontiersin.org/articles/10.3389/fimmu.2021.601080/fullCOVID-19T cellsSARS-CoV-2immunomonitoringdisease severity assessment
collection DOAJ
language English
format Article
sources DOAJ
author Chang-Feng Chu
Chang-Feng Chu
Chang-Feng Chu
Florian Sabath
Silvia Fibi-Smetana
Shan Sun
Shan Sun
Rupert Öllinger
Elfriede Noeßner
Ying-Yin Chao
Ying-Yin Chao
Linus Rinke
Elena Winheim
Roland Rad
Anne B. Krug
Leila Taher
Christina E. Zielinski
Christina E. Zielinski
Christina E. Zielinski
spellingShingle Chang-Feng Chu
Chang-Feng Chu
Chang-Feng Chu
Florian Sabath
Silvia Fibi-Smetana
Shan Sun
Shan Sun
Rupert Öllinger
Elfriede Noeßner
Ying-Yin Chao
Ying-Yin Chao
Linus Rinke
Elena Winheim
Roland Rad
Anne B. Krug
Leila Taher
Christina E. Zielinski
Christina E. Zielinski
Christina E. Zielinski
Convalescent COVID-19 Patients Without Comorbidities Display Similar Immunophenotypes Over Time Despite Divergent Disease Severities
Frontiers in Immunology
COVID-19
T cells
SARS-CoV-2
immunomonitoring
disease severity assessment
author_facet Chang-Feng Chu
Chang-Feng Chu
Chang-Feng Chu
Florian Sabath
Silvia Fibi-Smetana
Shan Sun
Shan Sun
Rupert Öllinger
Elfriede Noeßner
Ying-Yin Chao
Ying-Yin Chao
Linus Rinke
Elena Winheim
Roland Rad
Anne B. Krug
Leila Taher
Christina E. Zielinski
Christina E. Zielinski
Christina E. Zielinski
author_sort Chang-Feng Chu
title Convalescent COVID-19 Patients Without Comorbidities Display Similar Immunophenotypes Over Time Despite Divergent Disease Severities
title_short Convalescent COVID-19 Patients Without Comorbidities Display Similar Immunophenotypes Over Time Despite Divergent Disease Severities
title_full Convalescent COVID-19 Patients Without Comorbidities Display Similar Immunophenotypes Over Time Despite Divergent Disease Severities
title_fullStr Convalescent COVID-19 Patients Without Comorbidities Display Similar Immunophenotypes Over Time Despite Divergent Disease Severities
title_full_unstemmed Convalescent COVID-19 Patients Without Comorbidities Display Similar Immunophenotypes Over Time Despite Divergent Disease Severities
title_sort convalescent covid-19 patients without comorbidities display similar immunophenotypes over time despite divergent disease severities
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2021-08-01
description COVID-19, the disease caused by SARS-CoV-2 infection, can assume a highly variable disease course, ranging from asymptomatic infection, which constitutes the majority of cases, to severe respiratory failure. This implies a diverse host immune response to SARS-CoV-2. However, the immunological underpinnings underlying these divergent disease courses remain elusive. We therefore set out to longitudinally characterize immune signatures of convalescent COVID-19 patients stratified according to their disease severity. Our unique convalescent COVID-19 cohort consists of 74 patients not confounded by comorbidities. This is the first study of which we are aware that excludes immune abrogations associated with non-SARS-CoV-2 related risk factors of disease severity. Patients were followed up and analyzed longitudinally (2, 4 and 6 weeks after infection) by high-dimensional flow cytometric profiling of peripheral blood mononuclear cells (PBMCs), in-depth serum analytics, and transcriptomics. Immune phenotypes were correlated to disease severity. Convalescence was overall associated with uniform immune signatures, but distinct immune signatures for mildly versus severely affected patients were detectable within a 2-week time window after infection.
topic COVID-19
T cells
SARS-CoV-2
immunomonitoring
disease severity assessment
url https://www.frontiersin.org/articles/10.3389/fimmu.2021.601080/full
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