IL-6 Inhibition in Critically Ill COVID-19 Patients Is Associated With Increased Secondary Infections
Background: Anti-inflammatory therapies such as IL-6 inhibition have been proposed for COVID-19 in a vacuum of evidence-based treatment. However, abrogating the inflammatory response in infectious diseases may impair a desired host response and pre-dispose to secondary infections.Methods: We retrosp...
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doaj-4909ef0b306f4a6bb05e1b479c9f701a2020-11-25T03:52:18ZengFrontiers Media S.A.Frontiers in Medicine2296-858X2020-10-01710.3389/fmed.2020.583897583897IL-6 Inhibition in Critically Ill COVID-19 Patients Is Associated With Increased Secondary InfectionsLucas M. Kimmig0Lucas M. Kimmig1David Wu2David Wu3Matthew Gold4Natasha N. Pettit5Natasha N. Pettit6David Pitrak7David Pitrak8Jeffrey Mueller9Aliya N. Husain10Ece A. Mutlu11Gökhan M. Mutlu12Gökhan M. Mutlu13Department of Medicine, University of Chicago, Chicago, IL, United StatesSection of Pulmonary and Critical Care Medicine, University of Chicago, Chicago, IL, United StatesDepartment of Medicine, University of Chicago, Chicago, IL, United StatesSection of Pulmonary and Critical Care Medicine, University of Chicago, Chicago, IL, United StatesDepartment of Medicine, University of Chicago, Chicago, IL, United StatesDepartment of Medicine, University of Chicago, Chicago, IL, United StatesSection of Infectious Diseases, University of Chicago, Chicago, IL, United StatesDepartment of Medicine, University of Chicago, Chicago, IL, United StatesSection of Infectious Diseases, University of Chicago, Chicago, IL, United StatesDepartment of Pathology, University of Chicago, Chicago, IL, United StatesDepartment of Pathology, University of Chicago, Chicago, IL, United StatesSection of Gastroenterology and Hepatology, Rush University, Chicago, IL, United StatesDepartment of Medicine, University of Chicago, Chicago, IL, United StatesSection of Pulmonary and Critical Care Medicine, University of Chicago, Chicago, IL, United StatesBackground: Anti-inflammatory therapies such as IL-6 inhibition have been proposed for COVID-19 in a vacuum of evidence-based treatment. However, abrogating the inflammatory response in infectious diseases may impair a desired host response and pre-dispose to secondary infections.Methods: We retrospectively reviewed the medical record of critically ill COVID-19 patients during an 8-week span and compared the prevalence of secondary infection and outcomes in patients who did and did not receive tocilizumab. Additionally, we included representative histopathologic post-mortem findings from several COVID-19 cases that underwent autopsy at our institution.Results: One hundred eleven patients were identified, of which 54 had received tocilizumab while 57 had not. Receiving tocilizumab was associated with a higher risk of secondary bacterial (48.1 vs. 28.1%; p = 0.029 and fungal (5.6 vs. 0%; p = 0.112) infections. Consistent with higher number of infections, patients who received tocilizumab had higher mortality (35.2 vs. 19.3%; p = 0.020). Seven cases underwent autopsy. In three cases who received tocilizumab, there was evidence of pneumonia on pathology. Of the four cases that had not been given tocilizumab, two showed evidence of aspiration pneumonia and two exhibited diffuse alveolar damage.Conclusions: Experimental therapies are currently being applied to COVID-19 outside of clinical trials. Anti-inflammatory therapies such as anti-IL-6 therapy have the potential to impair viral clearance, pre-dispose to secondary infection, and cause harm. We seek to raise physician awareness of these issues and highlight the need to better understand the immune response in COVID-19.https://www.frontiersin.org/articles/10.3389/fmed.2020.583897/fullCOVID-19SARS-CoV-2tocilizumabcytokine release syndromeimmunosuppression |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lucas M. Kimmig Lucas M. Kimmig David Wu David Wu Matthew Gold Natasha N. Pettit Natasha N. Pettit David Pitrak David Pitrak Jeffrey Mueller Aliya N. Husain Ece A. Mutlu Gökhan M. Mutlu Gökhan M. Mutlu |
spellingShingle |
Lucas M. Kimmig Lucas M. Kimmig David Wu David Wu Matthew Gold Natasha N. Pettit Natasha N. Pettit David Pitrak David Pitrak Jeffrey Mueller Aliya N. Husain Ece A. Mutlu Gökhan M. Mutlu Gökhan M. Mutlu IL-6 Inhibition in Critically Ill COVID-19 Patients Is Associated With Increased Secondary Infections Frontiers in Medicine COVID-19 SARS-CoV-2 tocilizumab cytokine release syndrome immunosuppression |
author_facet |
Lucas M. Kimmig Lucas M. Kimmig David Wu David Wu Matthew Gold Natasha N. Pettit Natasha N. Pettit David Pitrak David Pitrak Jeffrey Mueller Aliya N. Husain Ece A. Mutlu Gökhan M. Mutlu Gökhan M. Mutlu |
author_sort |
Lucas M. Kimmig |
title |
IL-6 Inhibition in Critically Ill COVID-19 Patients Is Associated With Increased Secondary Infections |
title_short |
IL-6 Inhibition in Critically Ill COVID-19 Patients Is Associated With Increased Secondary Infections |
title_full |
IL-6 Inhibition in Critically Ill COVID-19 Patients Is Associated With Increased Secondary Infections |
title_fullStr |
IL-6 Inhibition in Critically Ill COVID-19 Patients Is Associated With Increased Secondary Infections |
title_full_unstemmed |
IL-6 Inhibition in Critically Ill COVID-19 Patients Is Associated With Increased Secondary Infections |
title_sort |
il-6 inhibition in critically ill covid-19 patients is associated with increased secondary infections |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Medicine |
issn |
2296-858X |
publishDate |
2020-10-01 |
description |
Background: Anti-inflammatory therapies such as IL-6 inhibition have been proposed for COVID-19 in a vacuum of evidence-based treatment. However, abrogating the inflammatory response in infectious diseases may impair a desired host response and pre-dispose to secondary infections.Methods: We retrospectively reviewed the medical record of critically ill COVID-19 patients during an 8-week span and compared the prevalence of secondary infection and outcomes in patients who did and did not receive tocilizumab. Additionally, we included representative histopathologic post-mortem findings from several COVID-19 cases that underwent autopsy at our institution.Results: One hundred eleven patients were identified, of which 54 had received tocilizumab while 57 had not. Receiving tocilizumab was associated with a higher risk of secondary bacterial (48.1 vs. 28.1%; p = 0.029 and fungal (5.6 vs. 0%; p = 0.112) infections. Consistent with higher number of infections, patients who received tocilizumab had higher mortality (35.2 vs. 19.3%; p = 0.020). Seven cases underwent autopsy. In three cases who received tocilizumab, there was evidence of pneumonia on pathology. Of the four cases that had not been given tocilizumab, two showed evidence of aspiration pneumonia and two exhibited diffuse alveolar damage.Conclusions: Experimental therapies are currently being applied to COVID-19 outside of clinical trials. Anti-inflammatory therapies such as anti-IL-6 therapy have the potential to impair viral clearance, pre-dispose to secondary infection, and cause harm. We seek to raise physician awareness of these issues and highlight the need to better understand the immune response in COVID-19. |
topic |
COVID-19 SARS-CoV-2 tocilizumab cytokine release syndrome immunosuppression |
url |
https://www.frontiersin.org/articles/10.3389/fmed.2020.583897/full |
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