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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Main Authors: Lucas M. Kimmig, David Wu, Matthew Gold, Natasha N. Pettit, David Pitrak, Jeffrey Mueller, Aliya N. Husain, Ece A. Mutlu, Gökhan M. Mutlu
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-10-01
Series:Frontiers in Medicine
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2020.583897/full
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spelling 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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