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Shedding of infectious SARS-CoV-2 by hospitalized COVID-19 patients in relation to serum antibody responses

BACKGROUND: Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is a global pandemic. The understanding of the transmission and the duration of viral shedding in SARS-CoV-2 infection is still limited. OBJECTIVES: To assess the timeframe and po...

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Autores principales: Glans, Hedvig, Gredmark-Russ, Sara, Olausson, Mikaela, Falck-Jones, Sara, Varnaite, Renata, Christ, Wanda, Maleki, Kimia T., Karlberg, Maria Lind, Broddesson, Sandra, Falck-Jones, Ryan, Bell, Max, Johansson, Niclas, Färnert, Anna, Smed-Sörensen, Anna, Klingström, Jonas, Bråve, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8159068/
https://www.ncbi.nlm.nih.gov/pubmed/34044758
http://dx.doi.org/10.1186/s12879-021-06202-8
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author Glans, Hedvig
Gredmark-Russ, Sara
Olausson, Mikaela
Falck-Jones, Sara
Varnaite, Renata
Christ, Wanda
Maleki, Kimia T.
Karlberg, Maria Lind
Broddesson, Sandra
Falck-Jones, Ryan
Bell, Max
Johansson, Niclas
Färnert, Anna
Smed-Sörensen, Anna
Klingström, Jonas
Bråve, Andreas
author_facet Glans, Hedvig
Gredmark-Russ, Sara
Olausson, Mikaela
Falck-Jones, Sara
Varnaite, Renata
Christ, Wanda
Maleki, Kimia T.
Karlberg, Maria Lind
Broddesson, Sandra
Falck-Jones, Ryan
Bell, Max
Johansson, Niclas
Färnert, Anna
Smed-Sörensen, Anna
Klingström, Jonas
Bråve, Andreas
author_sort Glans, Hedvig
collection PubMed
description BACKGROUND: Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is a global pandemic. The understanding of the transmission and the duration of viral shedding in SARS-CoV-2 infection is still limited. OBJECTIVES: To assess the timeframe and potential risk of SARS-CoV-2 transmission from hospitalized COVID-19 patients in relation to antibody response. METHOD: We performed a cross-sectional study of 36 COVID-19 patients hospitalized at Karolinska University Hospital. Patients with more than 8 days of symptom duration were sampled from airways, for PCR analysis of SARS-CoV-2 RNA and in vitro culture of replicating virus. Serum SARS-CoV-2-specific immunoglobulin G (IgG) and neutralizing antibodies titers were assessed by immunofluorescence assay (IFA) and microneutralization assay. RESULTS: SARS-CoV-2 RNA was detected in airway samples in 23 patients (symptom duration median 15 days, range 9–53 days), whereas 13 patients were SARS-CoV-2 RNA negative (symptom duration median 21 days, range 10–37 days). Replicating virus was detected in samples from 4 patients at 9–16 days. All but two patients had detectable levels of SARS-CoV-2-specific IgG in serum, and SARS-CoV-2 neutralizing antibodies were detected in 33 out of 36 patients. Total SARS-CoV-2-specific IgG titers and neutralizing antibody titers were positively correlated. High levels of both total IgG and neutralizing antibody titers were observed in patients sampled later after symptom onset and in patients where replicating virus could not be detected. CONCLUSIONS: Our data suggest that the presence of SARS-Cov-2 specific antibodies in serum may indicate a lower risk of shedding infectious SARS-CoV-2 by hospitalized COVID-19 patients.
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spelling pubmed-81590682021-05-28 Shedding of infectious SARS-CoV-2 by hospitalized COVID-19 patients in relation to serum antibody responses Glans, Hedvig Gredmark-Russ, Sara Olausson, Mikaela Falck-Jones, Sara Varnaite, Renata Christ, Wanda Maleki, Kimia T. Karlberg, Maria Lind Broddesson, Sandra Falck-Jones, Ryan Bell, Max Johansson, Niclas Färnert, Anna Smed-Sörensen, Anna Klingström, Jonas Bråve, Andreas BMC Infect Dis Research BACKGROUND: Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is a global pandemic. The understanding of the transmission and the duration of viral shedding in SARS-CoV-2 infection is still limited. OBJECTIVES: To assess the timeframe and potential risk of SARS-CoV-2 transmission from hospitalized COVID-19 patients in relation to antibody response. METHOD: We performed a cross-sectional study of 36 COVID-19 patients hospitalized at Karolinska University Hospital. Patients with more than 8 days of symptom duration were sampled from airways, for PCR analysis of SARS-CoV-2 RNA and in vitro culture of replicating virus. Serum SARS-CoV-2-specific immunoglobulin G (IgG) and neutralizing antibodies titers were assessed by immunofluorescence assay (IFA) and microneutralization assay. RESULTS: SARS-CoV-2 RNA was detected in airway samples in 23 patients (symptom duration median 15 days, range 9–53 days), whereas 13 patients were SARS-CoV-2 RNA negative (symptom duration median 21 days, range 10–37 days). Replicating virus was detected in samples from 4 patients at 9–16 days. All but two patients had detectable levels of SARS-CoV-2-specific IgG in serum, and SARS-CoV-2 neutralizing antibodies were detected in 33 out of 36 patients. Total SARS-CoV-2-specific IgG titers and neutralizing antibody titers were positively correlated. High levels of both total IgG and neutralizing antibody titers were observed in patients sampled later after symptom onset and in patients where replicating virus could not be detected. CONCLUSIONS: Our data suggest that the presence of SARS-Cov-2 specific antibodies in serum may indicate a lower risk of shedding infectious SARS-CoV-2 by hospitalized COVID-19 patients. BioMed Central 2021-05-27 /pmc/articles/PMC8159068/ /pubmed/34044758 http://dx.doi.org/10.1186/s12879-021-06202-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Glans, Hedvig
Gredmark-Russ, Sara
Olausson, Mikaela
Falck-Jones, Sara
Varnaite, Renata
Christ, Wanda
Maleki, Kimia T.
Karlberg, Maria Lind
Broddesson, Sandra
Falck-Jones, Ryan
Bell, Max
Johansson, Niclas
Färnert, Anna
Smed-Sörensen, Anna
Klingström, Jonas
Bråve, Andreas
Shedding of infectious SARS-CoV-2 by hospitalized COVID-19 patients in relation to serum antibody responses
title Shedding of infectious SARS-CoV-2 by hospitalized COVID-19 patients in relation to serum antibody responses
title_full Shedding of infectious SARS-CoV-2 by hospitalized COVID-19 patients in relation to serum antibody responses
title_fullStr Shedding of infectious SARS-CoV-2 by hospitalized COVID-19 patients in relation to serum antibody responses
title_full_unstemmed Shedding of infectious SARS-CoV-2 by hospitalized COVID-19 patients in relation to serum antibody responses
title_short Shedding of infectious SARS-CoV-2 by hospitalized COVID-19 patients in relation to serum antibody responses
title_sort shedding of infectious sars-cov-2 by hospitalized covid-19 patients in relation to serum antibody responses
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8159068/
https://www.ncbi.nlm.nih.gov/pubmed/34044758
http://dx.doi.org/10.1186/s12879-021-06202-8
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