Abstract

BackgroundThe clinical presentation of severe acute respiratory syndrome coronavirus-2 infection is highly variable from asymptomatic infection to fulminant disease. The reasons for the variation are only starting to unravel, with risk factors including age and certain comorbidities as well as genetic defects causing immunological perturbations in the interferon pathways.Case presentationWe report the case of an otherwise healthy Caucasian man, who at ages 60 and 64 years suffered from severe H1N1 influenza virus infection and severe acute respiratory syndrome coronavirus-2 infections, respectively. In both cases, there were acute kidney impairment and the need for intensive care unit admission as well as mechanical ventilation. Fortunately, after both infections there was full clinical recovery. The severity of the infections indicates an underlying impairment in the ability to control these kinds of infections. Challenge of patient peripheral blood mononuclear cells showed impaired type I and III antiviral interferon responses and reduced interferon-stimulated gene expression. However, despite investigation of patient samples by whole exome sequencing and enzyme-linked immunosorbent assay, no known disease-causing genetic variants related to interferon pathways were found, nor were interferon autoantibodies demonstrated. Thus, any underlying immunological cause of this unusual susceptibility to severe viral infections remains unresolved.ConclusionThe patient experienced very similar severe clinical pictures triggered by H1N1 and severe acute respiratory syndrome coronavirus-2 infections, indicating an underlying inability to contain these infections. We were unable to show that the patient had any of the currently known types of immune incompetence but identified genetic changes possibly contributing to the severe course of both infections. Further analyses to delineate contribution factors are needed.

Highlights

  • The clinical course of coronavirus disease 2019 (COVID19) is highly variable

  • The patient experienced very similar severe clinical pictures triggered by Hemagglutinin 1 (H1N1) and severe acute respiratory syndrome coronavirus-2 infections, indicating an underlying inability to contain these infections

  • It has recently been shown that genetic defects in the toll-like receptor (TLR)-3 and -7 dependent type I interferon (IFN) pathway as well as IFN autoantibodies are highly enriched among patients with life-threatening COVID-19 [3,4,5]

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Summary

Introduction

The clinical course of coronavirus disease 2019 (COVID19) is highly variable. The reasons behind this are only starting to be elucidated. We report an otherwise healthy man who, with an interval of 4 years, suffered first fulminant H1N1 and later severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections, with full recovery after both, indicating an underlying weakness in the defense against these types of viral infections. Case presentation: We report the case of an otherwise healthy Caucasian man, who at ages 60 and 64 years suffered from severe H1N1 influenza virus infection and severe acute respiratory syndrome coronavirus-2 infections, respectively. In both cases, there were acute kidney impairment and the need for intensive care unit admission as well as mechanical ventilation. Any underlying immunological cause of this unusual susceptibility to severe viral infections remains unresolved

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