Publication:
Critically ill COVID-19 patients with neutralizing autoantibodies against type I interferons have increased risk of herpesvirus disease.

cris.virtualsource.author-orcidc6752d14-6930-407c-bcb9-e0fb392a14aa
datacite.rightsopen.access
dc.contributor.authorBusnadiego, Idoia
dc.contributor.authorAbela, Irene A
dc.contributor.authorFrey, Pascal Marcel
dc.contributor.authorHofmaenner, Daniel A
dc.contributor.authorScheier, Thomas C
dc.contributor.authorSchuepbach, Reto A
dc.contributor.authorBuehler, Philipp K
dc.contributor.authorBrugger, Silvio D
dc.contributor.authorHale, Benjamin G
dc.date.accessioned2024-10-11T16:47:08Z
dc.date.available2024-10-11T16:47:08Z
dc.date.issued2022-07
dc.description.abstractAutoantibodies neutralizing the antiviral action of type I interferons (IFNs) have been associated with predisposition to severe Coronavirus Disease 2019 (COVID-19). Here, we screened for such autoantibodies in 103 critically ill COVID-19 patients in a tertiary intensive care unit (ICU) in Switzerland. Eleven patients (10.7%), but no healthy donors, had neutralizing anti-IFNα or anti-IFNα/anti-IFNω IgG in plasma/serum, but anti-IFN IgM or IgA was rare. One patient had nonneutralizing anti-IFNα IgG. Strikingly, all patients with plasma anti-IFNα IgG also had anti-IFNα IgG in tracheobronchial secretions, identifying these autoantibodies at anatomical sites relevant for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection. Longitudinal analyses revealed patient heterogeneity in terms of increasing, decreasing, or stable anti-IFN IgG levels throughout the length of hospitalization. Notably, presence of anti-IFN autoantibodies in this critically ill COVID-19 cohort appeared to predict herpesvirus disease (caused by herpes simplex viruses types 1 and 2 (HSV-1/-2) and/or cytomegalovirus (CMV)), which has been linked to worse clinical outcomes. Indeed, all 7 tested COVID-19 patients with anti-IFN IgG in our cohort (100%) suffered from one or more herpesviruses, and analysis revealed that these patients were more likely to experience CMV than COVID-19 patients without anti-IFN autoantibodies, even when adjusting for age, gender, and systemic steroid treatment (odds ratio (OR) 7.28, 95% confidence interval (CI) 1.14 to 46.31, p = 0.036). As the IFN system deficiency caused by neutralizing anti-IFN autoantibodies likely directly and indirectly exacerbates the likelihood of latent herpesvirus reactivations in critically ill patients, early diagnosis of anti-IFN IgG could be rapidly used to inform risk-group stratification and treatment options. Trial Registration: ClinicalTrials.gov Identifier: NCT04410263.
dc.description.numberOfPages16
dc.description.sponsorshipUniversitätsklinik für Allgemeine Innere Medizin
dc.identifier.doi10.48350/171112
dc.identifier.pmid35788562
dc.identifier.publisherDOI10.1371/journal.pbio.3001709
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/85988
dc.language.isoen
dc.publisherPublic Library of Science
dc.relation.ispartofPLoS biology
dc.relation.issn1544-9173
dc.relation.organizationClinic of General Internal Medicine
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleCritically ill COVID-19 patients with neutralizing autoantibodies against type I interferons have increased risk of herpesvirus disease.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue7
oaire.citation.startPagee3001709
oaire.citation.volume20
oairecerif.author.affiliationUniversitätsklinik für Allgemeine Innere Medizin
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unibe.date.licenseChanged2022-07-06 08:30:58
unibe.description.ispublishedpub
unibe.eprints.legacyId171112
unibe.journal.abbrevTitlePLOS BIOL
unibe.refereedtrue
unibe.subtype.articlejournal

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