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Fulminant H1N1 and severe acute respiratory syndrome coronavirus-2 infections with a 4-year interval without an identifiable underlying cause: a case report.
Katzenstein, Terese L; Jørgensen, Sofie E; Mortensen, Jann; Helleberg, Marie; Kalhauge, Anna; Mogensen, Trine H.
  • Katzenstein TL; Department of Infectious Diseases, Copenhagen University Hospital, Rigshospitalet, Esther Moellers vej 6, 2100, Copenhagen, Denmark. terese.katzenstein@regionh.dk.
  • Jørgensen SE; Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
  • Mortensen J; Department of Clinical Physiology and Nuclear Medicine, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
  • Helleberg M; Department of Infectious Diseases, Copenhagen University Hospital, Rigshospitalet, Esther Moellers vej 6, 2100, Copenhagen, Denmark.
  • Kalhauge A; Department of Radiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
  • Mogensen TH; Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
J Med Case Rep ; 15(1): 505, 2021 Oct 08.
Article in English | MEDLINE | ID: covidwho-1463266
ABSTRACT

BACKGROUND:

The 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 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. 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.

CONCLUSION:

The 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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Severe acute respiratory syndrome-related coronavirus / Influenza A Virus, H1N1 Subtype / COVID-19 Type of study: Case report / Observational study / Prognostic study Topics: Variants Limits: Humans / Male / Middle aged Language: English Journal: J Med Case Rep Year: 2021 Document Type: Article Affiliation country: S13256-021-03113-9

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Severe acute respiratory syndrome-related coronavirus / Influenza A Virus, H1N1 Subtype / COVID-19 Type of study: Case report / Observational study / Prognostic study Topics: Variants Limits: Humans / Male / Middle aged Language: English Journal: J Med Case Rep Year: 2021 Document Type: Article Affiliation country: S13256-021-03113-9