Immune transcriptomes of highly exposed SARS-CoV-2 asymptomatic seropositive versus seronegative individuals from the Ischgl community

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作者
Hye Kyung Lee
Ludwig Knabl
Lisa Pipperger
Andre Volland
Priscilla A. Furth
Keunsoo Kang
Harold E. Smith
Ludwig Knabl
Romuald Bellmann
Christina Bernhard
Norbert Kaiser
Hannes Gänzer
Mathias Ströhle
Andreas Walser
Dorothee von Laer
Lothar Hennighausen
机构
[1] National Institute of Diabetes,Laboratory of Cell and Molecular Biology
[2] Digestive and Kidney Diseases,Institute of Hygiene and Medical Microbiology & Institute of Virology, Department of Hygiene, Microbiology and Public Health
[3] Medical University of Innsbruck,Departments of Oncology and Medicine, Lombardi Comprehensive Cancer Center
[4] Pathologie-Labor,Department of Microbiology
[5] Georgetown University,Clinical Pharmacokinetics Unit, Division of Intensive Care and Emergency Medicine, Department of Internal Medicine I
[6] Dankook University,Intensive Care
[7] Krankenhaus St.Vinzenz Zams,undefined
[8] Medical University Innsbruck,undefined
[9] Hospital Kufstein,undefined
[10] Bezirkskrankenhaus St. Johann in Tirol,undefined
[11] Bezirkskrankenhaus Schwaz,undefined
[12] Medical University of Innsbruck,undefined
[13] Ordination (Private Practice),undefined
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摘要
SARS-CoV-2 infection ranges from asymptomatic to severe with lingering symptomatology in some. This prompted investigation of whether or not asymptomatic disease results in measurable immune activation post-infection. Immune activation following asymptomatic SARS-CoV-2 infection was characterized through a comparative investigation of the immune cell transcriptomes from 43 asymptomatic seropositive and 52 highly exposed seronegative individuals from the same community 4–6 weeks following a superspreading event. Few of the 95 individuals had underlying health issues. One seropositive individual reported Cystic Fibrosis and one individual reported Incontinentia pigmenti. No evidence of immune activation was found in asymptomatic seropositive individuals with the exception of the Cystic Fibrosis patient. There were no statistically significant differences in immune transcriptomes between asymptomatic seropositive and highly exposed seronegative individuals. Four positive controls, mildly symptomatic seropositive individuals whose blood was examined 3 weeks following infection, showed immune activation. Negative controls were four seronegative individuals from neighboring communities without COVID-19. All individuals remained in their usual state of health through a five-month follow-up after sample collection. In summary, whole blood transcriptomes identified individual immune profiles within a community population and showed that asymptomatic infection within a super-spreading event was not associated with enduring immunological activation.
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