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Protective reactive thymus hyperplasia in COVID-19 acute respiratory distress syndrome

BACKGROUND: Patients with COVID-19 (COVID) may develop acute respiratory distress syndrome with or without sepsis, coagulopathy and visceral damage. While chest CT scans are routinely performed in the initial assessment of patients with severe pulmonary forms, thymus involvement and reactivation hav...

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Autores principales: Cuvelier, Pelagia, Roux, Hélène, Couëdel-Courteille, Anne, Dutrieux, Jacques, Naudin, Cécile, Charmeteau de Muylder, Bénédicte, Cheynier, Rémi, Squara, Pierre, Marullo, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7781174/
https://www.ncbi.nlm.nih.gov/pubmed/33397460
http://dx.doi.org/10.1186/s13054-020-03440-1
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author Cuvelier, Pelagia
Roux, Hélène
Couëdel-Courteille, Anne
Dutrieux, Jacques
Naudin, Cécile
Charmeteau de Muylder, Bénédicte
Cheynier, Rémi
Squara, Pierre
Marullo, Stefano
author_facet Cuvelier, Pelagia
Roux, Hélène
Couëdel-Courteille, Anne
Dutrieux, Jacques
Naudin, Cécile
Charmeteau de Muylder, Bénédicte
Cheynier, Rémi
Squara, Pierre
Marullo, Stefano
author_sort Cuvelier, Pelagia
collection PubMed
description BACKGROUND: Patients with COVID-19 (COVID) may develop acute respiratory distress syndrome with or without sepsis, coagulopathy and visceral damage. While chest CT scans are routinely performed in the initial assessment of patients with severe pulmonary forms, thymus involvement and reactivation have not been investigated so far. METHODS: In this observational study, we systematically scored the enlargement of the thymus and the lung involvement, using CT scans, in all adult patients admitted to the ICU for COVID or any other cause (control group) at one centre between March and April 2020. Initial biological investigations included nasal detection of SARS-CoV-2 ribonucleic acid by polymerase chain reaction (PCR). In a subgroup of 24 patients with different degrees of pulmonary involvement and thymus hypertrophy, plasma cytokine concentrations were measured and the export of mature T cells from the thymus was estimated simultaneously by PCR quantification of T cell receptor excision circles (TRECs). RESULTS: Eighty-seven patients were studied: 50 COVID patients and 37 controls. Non-atrophic or enlarged thymus was more commonly observed in COVID patients than in controls (66% vs. 24%, p < 0.0001). Thymus enlargement in COVID patients was associated with more extensive lung injury score on CT scans (4 [3–5] vs. 2 [1.5–4], p = 0.01), but a lower mortality rate (8.6% vs. 41.2%, p < 0.001). Other factors associated with mortality were age, lymphopaenia, high CRP and co-morbidities. COVID patients had higher concentrations of IL-7 (6.00 [3.72–9.25] vs. 2.17 [1.76–4.4] pg/mL; p = 0.04) and higher thymic production of new lymphocytes (sj/βTREC ratio = 2.88 [1.98–4.51] vs. 0.23 [0.15–0.60]; p = 0.004). Thymic production was also correlated with the CT scan thymic score (r = 0.38, p = 0.03) and inversely correlated with the number of lymphocytes (r = 0.56, p = 0.007). CONCLUSION: In COVID patients, thymus enlargement was frequent and associated with increased T lymphocyte production, which appears to be a beneficial adaptation to virus-induced lymphopaenia. The lack of thymic activity/reactivation in older SARS-CoV-2 infected patients could contribute to a worse prognosis. [Image: see text]
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spelling pubmed-77811742021-01-05 Protective reactive thymus hyperplasia in COVID-19 acute respiratory distress syndrome Cuvelier, Pelagia Roux, Hélène Couëdel-Courteille, Anne Dutrieux, Jacques Naudin, Cécile Charmeteau de Muylder, Bénédicte Cheynier, Rémi Squara, Pierre Marullo, Stefano Crit Care Research BACKGROUND: Patients with COVID-19 (COVID) may develop acute respiratory distress syndrome with or without sepsis, coagulopathy and visceral damage. While chest CT scans are routinely performed in the initial assessment of patients with severe pulmonary forms, thymus involvement and reactivation have not been investigated so far. METHODS: In this observational study, we systematically scored the enlargement of the thymus and the lung involvement, using CT scans, in all adult patients admitted to the ICU for COVID or any other cause (control group) at one centre between March and April 2020. Initial biological investigations included nasal detection of SARS-CoV-2 ribonucleic acid by polymerase chain reaction (PCR). In a subgroup of 24 patients with different degrees of pulmonary involvement and thymus hypertrophy, plasma cytokine concentrations were measured and the export of mature T cells from the thymus was estimated simultaneously by PCR quantification of T cell receptor excision circles (TRECs). RESULTS: Eighty-seven patients were studied: 50 COVID patients and 37 controls. Non-atrophic or enlarged thymus was more commonly observed in COVID patients than in controls (66% vs. 24%, p < 0.0001). Thymus enlargement in COVID patients was associated with more extensive lung injury score on CT scans (4 [3–5] vs. 2 [1.5–4], p = 0.01), but a lower mortality rate (8.6% vs. 41.2%, p < 0.001). Other factors associated with mortality were age, lymphopaenia, high CRP and co-morbidities. COVID patients had higher concentrations of IL-7 (6.00 [3.72–9.25] vs. 2.17 [1.76–4.4] pg/mL; p = 0.04) and higher thymic production of new lymphocytes (sj/βTREC ratio = 2.88 [1.98–4.51] vs. 0.23 [0.15–0.60]; p = 0.004). Thymic production was also correlated with the CT scan thymic score (r = 0.38, p = 0.03) and inversely correlated with the number of lymphocytes (r = 0.56, p = 0.007). CONCLUSION: In COVID patients, thymus enlargement was frequent and associated with increased T lymphocyte production, which appears to be a beneficial adaptation to virus-induced lymphopaenia. The lack of thymic activity/reactivation in older SARS-CoV-2 infected patients could contribute to a worse prognosis. [Image: see text] BioMed Central 2021-01-04 /pmc/articles/PMC7781174/ /pubmed/33397460 http://dx.doi.org/10.1186/s13054-020-03440-1 Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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
Cuvelier, Pelagia
Roux, Hélène
Couëdel-Courteille, Anne
Dutrieux, Jacques
Naudin, Cécile
Charmeteau de Muylder, Bénédicte
Cheynier, Rémi
Squara, Pierre
Marullo, Stefano
Protective reactive thymus hyperplasia in COVID-19 acute respiratory distress syndrome
title Protective reactive thymus hyperplasia in COVID-19 acute respiratory distress syndrome
title_full Protective reactive thymus hyperplasia in COVID-19 acute respiratory distress syndrome
title_fullStr Protective reactive thymus hyperplasia in COVID-19 acute respiratory distress syndrome
title_full_unstemmed Protective reactive thymus hyperplasia in COVID-19 acute respiratory distress syndrome
title_short Protective reactive thymus hyperplasia in COVID-19 acute respiratory distress syndrome
title_sort protective reactive thymus hyperplasia in covid-19 acute respiratory distress syndrome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7781174/
https://www.ncbi.nlm.nih.gov/pubmed/33397460
http://dx.doi.org/10.1186/s13054-020-03440-1
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