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SARS-CoV-2-specific B- and T-cell immunity in a population-based study of young Swedish adults.
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.
  • Björkander S; Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
  • Du L; Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden.
  • Zuo F; Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden.
  • Ekström S; Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden; Center of Occupational and Environmental Medicine, Region Stockholm, Stockholm, Sweden.
  • Wang Y; Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden.
  • Wan H; Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden.
  • Sherina N; Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden.
  • Schoutens L; Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden.
  • Andréll J; Science for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, Stockholm, Sweden.
  • Andersson N; Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
  • Georgelis A; Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden; Center of Occupational and Environmental Medicine, Region Stockholm, Stockholm, Sweden.
  • Bergström A; Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden; Center of Occupational and Environmental Medicine, Region Stockholm, Stockholm, Sweden.
  • Marcotte H; Division of Clinical Immunology and Transfusion Medicine, Department of Laboratory Medicine, Karolinska Institutet at Karolinska University Hospital, Stockholm, Sweden.
  • Kull I; Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden; Sachs' Children and Youth Hospital, Södersjukhuset, Stockholm, Sweden.
  • Hammarström L; Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden.
  • Melén E; Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden; Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden; Sachs' Children and Youth Hospital, Södersjukhuset, Stockholm, Sweden. Electronic address: erik.melen@ki.se.
  • Pan-Hammarström Q; Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden. Electronic address: qiang.pan-hammarstrom@ki.se.
J Allergy Clin Immunol ; 149(1): 65-75.e8, 2022 Jan.
Article in English | MEDLINE | ID: covidwho-1474660
ABSTRACT

BACKGROUND:

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.

OBJECTIVE:

We conducted a population-based study on humoral and cellular immunity to SARS-CoV-2 and explored COVID-19 disease characteristics in young adults.

METHODS:

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.

RESULTS:

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.

CONCLUSIONS:

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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Full text: Available Collection: International databases Database: MEDLINE Main subject: T-Lymphocytes / Immunity, Humoral / SARS-CoV-2 / COVID-19 / Memory B Cells / Immunity, Cellular Type of study: Cohort study / Observational study / Prognostic study Topics: Long Covid / Vaccines Limits: Adult / Female / Humans / Male Country/Region as subject: Europa Language: English Journal: J Allergy Clin Immunol Year: 2022 Document Type: Article Affiliation country: J.jaci.2021.10.014

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Full text: Available Collection: International databases Database: MEDLINE Main subject: T-Lymphocytes / Immunity, Humoral / SARS-CoV-2 / COVID-19 / Memory B Cells / Immunity, Cellular Type of study: Cohort study / Observational study / Prognostic study Topics: Long Covid / Vaccines Limits: Adult / Female / Humans / Male Country/Region as subject: Europa Language: English Journal: J Allergy Clin Immunol Year: 2022 Document Type: Article Affiliation country: J.jaci.2021.10.014