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Cytokine levels associated with favorable clinical outcome in the CAPSID randomized trial of convalescent plasma in patients with severe COVID-19.
Körper, Sixten; Schrezenmeier, Eva Vanessa; Rincon-Arevalo, Hector; Grüner, Beate; Zickler, Daniel; Weiss, Manfred; Wiesmann, Thomas; Zacharowski, Kai; Kalbhenn, Johannes; Bentz, Martin; Dollinger, Matthias M; Paul, Gregor; Lepper, Philipp M; Ernst, Lucas; Wulf, Hinnerk; Zinn, Sebastian; Appl, Thomas; Jahrsdörfer, Bernd; Rojewski, Markus; Lotfi, Ramin; Dörner, Thomas; Jungwirth, Bettina; Seifried, Erhard; Fürst, Daniel; Schrezenmeier, Hubert.
  • Körper S; Institute for Clinical Transfusion Medicine and Immunogenetics Ulm, German Red Cross Blood Transfusion Service Baden-Württemberg-Hessen and University Hospital Ulm and Institute of Transfusion Medicine, University of Ulm, Ulm, Germany.
  • Schrezenmeier EV; Department of Nephrology and Medical Intensive Care, Charité - Universitätsmedizin Berlin, corporate member of Free University Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
  • Rincon-Arevalo H; Berlin Institute of Health Charité Universitätsmedizin Berlin, Berlin Institute of Health (BIH) Academy, Berlin, Germany.
  • Grüner B; Department of Nephrology and Medical Intensive Care, Charité - Universitätsmedizin Berlin, corporate member of Free University Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
  • Zickler D; Grupo de Inmunología Celular e Inmunogenética, Facultad de Medicina, Instituto de Investigaciones Médicas, Universidad de Antioquia UdeA, Medellín, Colombia.
  • Weiss M; Division of Infectious Diseases, University Hospital and Medical Center Ulm, Ulm, Germany.
  • Wiesmann T; Department of Nephrology and Medical Intensive Care, Charité - Universitätsmedizin Berlin, corporate member of Free University Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
  • Zacharowski K; Department of Anaesthesiology and Intensive Care Medicine, University Hospital Ulm, Ulm University, Ulm, Germany.
  • Kalbhenn J; Department of Anaesthesiology and Intensive Care Medicine, Phillips-University Marburg, Marburg, Germany.
  • Bentz M; Clinic of Anaesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt, Frankfurt, Germany.
  • Dollinger MM; Clinic of Anesthesiology and Intensive Care Medicine University Medical Center of Freiburg, Freiburg, Germany.
  • Paul G; Department of Internal Medicine III, Hospital of Karlsruhe, Karlsruhe, Germany.
  • Lepper PM; Medical Clinic I, Klinikum Landshut, Landshut, Germany.
  • Ernst L; Department of Gastroenterology, Hepatology, Pneumology and Infectious Diseases, Klinikum Stuttgart, Stuttgart, Germany.
  • Wulf H; Department of Internal Medicine V - Pneumology, Allergology, Intensive Care Medicine, Saarland University Hospital, Homburg, Germany.
  • Zinn S; Department of Nephrology and Medical Intensive Care, Charité - Universitätsmedizin Berlin, corporate member of Free University Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
  • Appl T; Department of Anaesthesiology and Intensive Care Medicine, University Hospital Ulm, Ulm University, Ulm, Germany.
  • Jahrsdörfer B; Department of Anaesthesiology and Intensive Care Medicine, Phillips-University Marburg, Marburg, Germany.
  • Rojewski M; Institute for Clinical Transfusion Medicine and Immunogenetics Ulm, German Red Cross Blood Transfusion Service Baden-Württemberg-Hessen and University Hospital Ulm and Institute of Transfusion Medicine, University of Ulm, Ulm, Germany.
  • Lotfi R; Institute for Clinical Transfusion Medicine and Immunogenetics Ulm, German Red Cross Blood Transfusion Service Baden-Württemberg-Hessen and University Hospital Ulm and Institute of Transfusion Medicine, University of Ulm, Ulm, Germany.
  • Dörner T; Institute for Clinical Transfusion Medicine and Immunogenetics Ulm, German Red Cross Blood Transfusion Service Baden-Württemberg-Hessen and University Hospital Ulm and Institute of Transfusion Medicine, University of Ulm, Ulm, Germany.
  • Jungwirth B; Institute for Clinical Transfusion Medicine and Immunogenetics Ulm, German Red Cross Blood Transfusion Service Baden-Württemberg-Hessen and University Hospital Ulm and Institute of Transfusion Medicine, University of Ulm, Ulm, Germany.
  • Seifried E; Department of Rheumatology and Clinical Immunology, Charité Universitätsmedizin Berlin, Berlin, Germany.
  • Fürst D; Deutsches Rheumaforschungszentrum (DRFZ), Berlin, Germany.
  • Schrezenmeier H; Department of Anaesthesiology and Intensive Care Medicine, University Hospital Ulm, Ulm University, Ulm, Germany.
Front Immunol ; 13: 1008438, 2022.
Статья в английский | MEDLINE | ID: covidwho-2080155
ABSTRACT

Objectives:

To determine the profile of cytokines in patients with severe COVID-19 who were enrolled in a trial of COVID-19 convalescent plasma (CCP).

Methods:

Patients were randomized to receive standard treatment and 3 CCP units or standard treatment alone (CAPSID trial, ClinicalTrials.gov NCT04433910). The primary outcome was a dichotomous composite outcome (survival and no longer severe COVID-19 on day 21). Time to clinical improvement was a key secondary endpoint. The concentrations of 27 cytokines were measured (baseline, day 7). We analyzed the change and the correlation between serum cytokine levels over time in different subgroups and the prediction of outcome in receiver operating characteristics (ROC) analyses and in multivariate models.

Results:

The majority of cytokines showed significant changes from baseline to day 7. Some were strongly correlated amongst each other (at baseline the cluster IL-1ß, IL-2, IL-6, IL-8, G-CSF, MIP-1α, the cluster PDGF-BB, RANTES or the cluster IL-4, IL-17, Eotaxin, bFGF, TNF-α). The correlation matrix substantially changed from baseline to day 7. The heatmaps of the absolute values of the correlation matrix indicated an association of CCP treatment and clinical outcome with the cytokine pattern. Low levels of IP-10, IFN-γ, MCP-1 and IL-1ß on day 0 were predictive of treatment success in a ROC analysis. In multivariate models, low levels of IL-1ß, IFN-γ and MCP-1 on day 0 were significantly associated with both treatment success and shorter time to clinical improvement. Low levels of IP-10, IL-1RA, IL-6, MCP-1 and IFN-γ on day 7 and high levels of IL-9, PDGF and RANTES on day 7 were predictive of treatment success in ROC analyses. Low levels of IP-10, MCP-1 and high levels of RANTES, on day 7 were associated with both treatment success and shorter time to clinical improvement in multivariate models.

Conclusion:

This analysis demonstrates a considerable dynamic of cytokines over time, which is influenced by both treatment and clinical course of COVID-19. Levels of IL-1ß and MCP-1 at baseline and MCP-1, IP-10 and RANTES on day 7 were associated with a favorable outcome across several endpoints. These cytokines should be included in future trials for further evaluation as predictive factors.
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Полный текст: Имеется в наличии Коллекция: Международные базы данных база данных: MEDLINE Основная тема: Cytokines / COVID-19 Тип исследования: Экспериментальные исследования / Прогностическое исследование / Рандомизированные контролируемые испытания Темы: Варианты Пределы темы: Люди Язык: английский Журнал: Front Immunol Год: 2022 Тип: Статья Аффилированная страна: Fimmu.2022.1008438

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Полный текст: Имеется в наличии Коллекция: Международные базы данных база данных: MEDLINE Основная тема: Cytokines / COVID-19 Тип исследования: Экспериментальные исследования / Прогностическое исследование / Рандомизированные контролируемые испытания Темы: Варианты Пределы темы: Люди Язык: английский Журнал: Front Immunol Год: 2022 Тип: Статья Аффилированная страна: Fimmu.2022.1008438