SARS-CoV-2–specific B- and T-cell immunity in a population-based study of young Swedish adults

Young adults are now considered major spreaders of coronavirus disease 2019 (COVID-19) disease. Although most young individuals experience mild to moderate disease, there are concerns of long-term adverse health effects. The impact of COVID-19 disease and to which extent population-level immunity ag...

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Published inJournal of allergy and clinical immunology Vol. 149; no. 1; pp. 65 - 75.e8
Main Authors Björkander, Sophia, Du, Likun, Zuo, Fanglei, Ekström, Sandra, Wang, Yating, Wan, Hui, Sherina, Natalia, Schoutens, Lisanne, Andréll, Juni, Andersson, Niklas, Georgelis, Antonios, Bergström, Anna, Marcotte, Harold, Kull, Inger, Hammarström, Lennart, Melén, Erik, Pan-Hammarström, Qiang, Almqvist, Catarina, Ballardini, Natalia, Brodin, Petter, Castel, Anna, Hallberg, Jenny, Jansson, Christer, Kere, Maura, Lauber, André, Lövquist, Alexandra, Mjösberg, Jenny, Mogensen, Ida, Palmberg, Lena, Pershagen, Göran, Roxhed, Niclas, Schwenk, Jochen
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.01.2022
The Authors. Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology
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Summary:Young adults are now considered major spreaders of coronavirus disease 2019 (COVID-19) disease. Although most young individuals experience mild to moderate disease, there are concerns of long-term adverse health effects. The impact of COVID-19 disease and to which extent population-level immunity against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) exists in young adults remain unclear. We conducted a population-based study on humoral and cellular immunity to SARS-CoV-2 and explored COVID-19 disease characteristics in young adults. We invited participants from the Swedish BAMSE (Barn [Children], Allergy Milieu, Stockholm, Epidemiology) birth cohort (age 24-27 years) to take part in a COVID-19 follow-up. From 980 participants (October 2020 to June 2021), we here present data on SARS-CoV-2 receptor-binding domain–specific IgM, IgA, and IgG titers measured by ELISA and on symptoms and epidemiologic factors associated with seropositivity. Further, SARS-CoV-2–specific memory B- and T-cell responses were detected for a subpopulation (n = 108) by ELISpot and FluoroSpot. A total of 28.4% of subjects were seropositive, of whom 18.4% were IgM single positive. One in 7 seropositive subjects was asymptomatic. Seropositivity was associated with use of public transport, but not with sex, asthma, rhinitis, IgE sensitization, smoking, or body mass index. In a subset of representative samples, 20.7% and 35.0% had detectable SARS-CoV-2 specific B- and T-cell responses, respectively. B- and T-cell memory responses were clearly associated with seropositivity, but T-cell responses were also detected in 17.2% of seronegative subjects. Assessment of IgM and T-cell responses may improve population-based estimations of SARS-CoV-2 infection. The pronounced surge of both symptomatic and asymptomatic infections among young adults indicates that the large-scale vaccination campaign should be continued.
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Members of the study group are listed in the acknowledgments.
ISSN:0091-6749
1097-6825
1097-6825
DOI:10.1016/j.jaci.2021.10.014