CMV seropositivity is a potential novel risk factor for severe COVID-19 in non-geriatric patients

BACKGROUND: COVID-19 has so far affected more than 250 million individuals worldwide, causing more than 5 million deaths. Several risk factors for severe disease have been identified, most of which coincide with advanced age. In younger individuals, severe COVID-19 often occurs in the absence of obvious comorbidities. Guided by the finding of cytomegalovirus (CMV)-specific T cells with some cross-reactivity to SARS-CoV-2 in a COVID-19 intensive care unit (ICU) patient, we decided to investigate whether CMV seropositivity is associated with severe or critical COVID-19. Herpes simplex virus (HSV) serostatus was investigated as control.

METHODS: National German COVID-19 bio-sample and data banks were used to retrospectively analyze the CMV and HSV serostatus of patients who experienced mild (n = 101), moderate (n = 130) or severe to critical (n = 80) disease by IgG serology. We then investigated the relationship between disease severity and herpesvirus serostatus via statistical models.

RESULTS: Non-geriatric patients (< 60 years) with severe COVID-19 were found to have a very high prevalence of CMV-seropositivity, while CMV status distribution in individuals with mild disease was similar to the prevalence in the German population; interestingly, this was not detectable in older patients. Prediction models support the hypothesis that the CMV serostatus, unlike HSV, might be a strong biomarker in identifying younger individuals with a higher risk of developing severe COVID-19, in particular in absence of other co-morbidities.

CONCLUSIONS: We identified 'CMV-seropositivity' as a potential novel risk factor for severe COVID-19 in non-geriatric individuals in the studied cohorts. More mechanistic analyses as well as confirmation of similar findings in cohorts representing the currently most relevant SARS-CoV-2 variants should be performed shortly.

Medienart:

E-Artikel

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

Zur Gesamtaufnahme - volume:17

Enthalten in:

PloS one - 17(2022), 5 vom: 10., Seite e0268530

Sprache:

Englisch

Beteiligte Personen:

Weber, Simone [VerfasserIn]
Kehl, Victoria [VerfasserIn]
Erber, Johanna [VerfasserIn]
Wagner, Karolin I [VerfasserIn]
Jetzlsperger, Ana-Marija [VerfasserIn]
Burrell, Teresa [VerfasserIn]
Schober, Kilian [VerfasserIn]
Schommers, Philipp [VerfasserIn]
Augustin, Max [VerfasserIn]
Crowell, Claudia S [VerfasserIn]
Gerhard, Markus [VerfasserIn]
Winter, Christof [VerfasserIn]
Moosmann, Andreas [VerfasserIn]
Spinner, Christoph D [VerfasserIn]
Protzer, Ulrike [VerfasserIn]
Hoffmann, Dieter [VerfasserIn]
D'Ippolito, Elvira [VerfasserIn]
Busch, Dirk H [VerfasserIn]

Links:

Volltext

Themen:

Antibodies, Viral
Journal Article
Research Support, Non-U.S. Gov't

Anmerkungen:

Date Completed 27.05.2022

Date Revised 16.07.2022

published: Electronic-eCollection

Citation Status MEDLINE

doi:

10.1371/journal.pone.0268530

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM341355283