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  3. Antibody and T-cell response to bivalent booster SARS-CoV-2 vaccines in people with compromised immune function (COVERALL-3).
 

Antibody and T-cell response to bivalent booster SARS-CoV-2 vaccines in people with compromised immune function (COVERALL-3).

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Description
Collaborators "Swiss Transplant Cohort Study": Annalisa Berzigotti, Guido Stirnimann , Vanessa Banz, Guido Beldi (UVCM Department of Visceral Surgery and Medicine)
BORIS DOI
10.48350/197683
Date of Publication
October 16, 2024
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Author
Amstutz, Alain
Chammartin, Frédérique
Audigé, Annette
Eichenberger, Anna
Universitätsklinik für Infektiologie
Braun, Dominique L
Amico, Patrizia
Stoeckle, Marcel P
Hasse, Barbara
Papadimitriou-Olivgeris, Matthaios
Manuel, Oriol
Bongard, Cédric
Schuurmans, Macé M
Hage, René
Damm, Dominik
Tamm, Michael
Mueller, Nicolas J
Rauch, Andriorcid-logo
Universitätsklinik für Infektiologie
Günthard, Huldrych F
Koller, Michael T
Schönenberger, Christof M
Griessbach, Alexandra
Labhardt, Niklaus D
Kouyos, Roger D
Trkola, Alexandra
Kusejko, Katharina
Bucher, Heiner C
Abela, Irene A
Briel, Matthias
Speich, Benjamin
Subject(s)

600 - Technology::610...

Series
The journal of infectious diseases
ISSN or ISBN (if monograph)
1537-6613
Publisher
Oxford University Press
Language
English
Publisher DOI
10.1093/infdis/jiae291
PubMed ID
38848312
Uncontrolled Keywords

COVID-19 HIV Organ tr...

Description
BACKGROUND

Bivalent mRNA vaccines, designed to combat emerging SARS-CoV-2 variants, incorporate ancestral strains and a new variant. Our study assessed the immune response in previously vaccinated individuals of the Swiss HIV Cohort Study (SHCS) and the Swiss Transplant Cohort Study (STCS) following bivalent mRNA vaccination.

METHODS

Eligible SHCS and STCS participants received approved bivalent mRNA SARS-CoV-2 vaccines (mRNA-1273.214 or BA.1-adapted BNT162b2) within clinical routine. Blood samples were collected at baseline, 4 weeks, 8 weeks, and 6 months post vaccination. We analyzed the proportion of participants with anti-spike protein antibody response ≥1642 units/ml (indicating protection against SARS-CoV-2 infection), and in a subsample T-cell response (including mean concentrations), stratifying results by cohorts and population characteristics.

RESULTS

In SHCS participants, baseline anti-spike antibody concentrations ≥1642 were observed in 87% (96/112), reaching nearly 100% at follow-ups. Among STCS participants, 58% (35/60) had baseline antibodies ≥1642, increasing to 80% at 6 months. Except for lung transplant recipients, all participants showed a five-fold increase in geometric mean antibody concentrations at 4 weeks and a reduction by half at 6 months. At baseline, T-cell responses were positive in 96% (26/27) of SHCS participants and 36% (16/45) of STCS participants (moderate increase to 53% at 6 months). Few participants reported SARS-CoV-2 infections, side-effects, or serious adverse events.

CONCLUSIONS

Bivalent mRNA vaccination elicited a robust humoral response in individuals with HIV or solid organ transplants, with delayed responses in lung transplant recipients. Despite a waning effect, antibody levels remained high at 6 months and adverse events were rare.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/178050
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