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Abstract
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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1 National Institute of Diabetes, Digestive and Kidney Diseases, Laboratory of Cell and Molecular Biology, Bethesda, USA (GRID:grid.419635.c) (ISNI:0000 0001 2203 7304)
2 Medical University of Innsbruck, Institute of Hygiene and Medical Microbiology & Institute of Virology, Department of Hygiene, Microbiology and Public Health, 6020 Innsbruck, Austria (GRID:grid.5361.1) (ISNI:0000 0000 8853 2677); Pathologie-Labor, 6020 Zams, Austria (GRID:grid.5361.1)
3 Medical University of Innsbruck, Institute of Hygiene and Medical Microbiology & Institute of Virology, Department of Hygiene, Microbiology and Public Health, 6020 Innsbruck, Austria (GRID:grid.5361.1) (ISNI:0000 0000 8853 2677)
4 Georgetown University, Departments of Oncology and Medicine, Lombardi Comprehensive Cancer Center, Washington, USA (GRID:grid.213910.8) (ISNI:0000 0001 1955 1644)
5 National Institute of Diabetes, Digestive and Kidney Diseases, Laboratory of Cell and Molecular Biology, Bethesda, USA (GRID:grid.419635.c) (ISNI:0000 0001 2203 7304); Dankook University, Department of Microbiology, Cheonan, South Korea (GRID:grid.411982.7) (ISNI:0000 0001 0705 4288)
6 Krankenhaus St.Vinzenz Zams, 6511 Zams, Austria (GRID:grid.419635.c)
7 Medical University Innsbruck, Clinical Pharmacokinetics Unit, Division of Intensive Care and Emergency Medicine, Department of Internal Medicine I, 6020 Innsbruck, Austria (GRID:grid.5361.1) (ISNI:0000 0000 8853 2677)
8 Hospital Kufstein, 6330 Kufstein, Austria (GRID:grid.5361.1)
9 Bezirkskrankenhaus St. Johann in Tirol, 6380 St. Johann in Tirol, Austria (GRID:grid.5361.1)
10 Bezirkskrankenhaus Schwaz, 6130 Schwaz, Austria (GRID:grid.5361.1)
11 Medical University of Innsbruck, Intensive Care, 6020 Innsbruck, Austria (GRID:grid.5361.1) (ISNI:0000 0000 8853 2677)
12 Ordination (Private Practice), 6561 Ischgl, Austria (GRID:grid.5361.1)