Publication: Critically ill COVID-19 patients with neutralizing autoantibodies against type I interferons have increased risk of herpesvirus disease.
| cris.virtualsource.author-orcid | c6752d14-6930-407c-bcb9-e0fb392a14aa | |
| datacite.rights | open.access | |
| dc.contributor.author | Busnadiego, Idoia | |
| dc.contributor.author | Abela, Irene A | |
| dc.contributor.author | Frey, Pascal Marcel | |
| dc.contributor.author | Hofmaenner, Daniel A | |
| dc.contributor.author | Scheier, Thomas C | |
| dc.contributor.author | Schuepbach, Reto A | |
| dc.contributor.author | Buehler, Philipp K | |
| dc.contributor.author | Brugger, Silvio D | |
| dc.contributor.author | Hale, Benjamin G | |
| dc.date.accessioned | 2024-10-11T16:47:08Z | |
| dc.date.available | 2024-10-11T16:47:08Z | |
| dc.date.issued | 2022-07 | |
| dc.description.abstract | Autoantibodies 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.numberOfPages | 16 | |
| dc.description.sponsorship | Universitätsklinik für Allgemeine Innere Medizin | |
| dc.identifier.doi | 10.48350/171112 | |
| dc.identifier.pmid | 35788562 | |
| dc.identifier.publisherDOI | 10.1371/journal.pbio.3001709 | |
| dc.identifier.uri | https://boris-portal.unibe.ch/handle/20.500.12422/85988 | |
| dc.language.iso | en | |
| dc.publisher | Public Library of Science | |
| dc.relation.ispartof | PLoS biology | |
| dc.relation.issn | 1544-9173 | |
| dc.relation.organization | Clinic of General Internal Medicine | |
| dc.subject.ddc | 600 - Technology::610 - Medicine & health | |
| dc.title | Critically ill COVID-19 patients with neutralizing autoantibodies against type I interferons have increased risk of herpesvirus disease. | |
| dc.type | article | |
| dspace.entity.type | Publication | |
| dspace.file.type | text | |
| oaire.citation.issue | 7 | |
| oaire.citation.startPage | e3001709 | |
| oaire.citation.volume | 20 | |
| oairecerif.author.affiliation | Universitätsklinik für Allgemeine Innere Medizin | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.date.licenseChanged | 2022-07-06 08:30:58 | |
| unibe.description.ispublished | pub | |
| unibe.eprints.legacyId | 171112 | |
| unibe.journal.abbrevTitle | PLOS BIOL | |
| unibe.refereed | true | |
| unibe.subtype.article | journal |
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