SARS-CoV-2 Neutralization Capacity in Hemodialysis Patients with and without a Fifth Vaccination with the Updated Comirnaty Original/Omicron BA.4-5 Vaccine.

BQ.1.1 Omicron BA.5 SARS-CoV-2 XBB.1.5 hemodialysis in vitro viral neutralization updated Comirnaty Original/Omicron BA.4-5 vaccine

Journal

Vaccines
ISSN: 2076-393X
Titre abrégé: Vaccines (Basel)
Pays: Switzerland
ID NLM: 101629355

Informations de publication

Date de publication:
15 Mar 2024
Historique:
received: 09 02 2024
revised: 10 03 2024
accepted: 12 03 2024
medline: 28 3 2024
pubmed: 28 3 2024
entrez: 28 3 2024
Statut: epublish

Résumé

Hemodialysis patients have reduced serologic immunity after SARS-CoV-2 vaccination compared to the general population and an increased risk of morbidity and mortality when exposed to SARS-CoV-2. Sixty-six hemodialysis patients immunized four times with the original SARS-CoV-2 vaccines (BNT162b2, mRNA-1273) either received a booster with the adapted Comirnaty Original/Omicron BA.4-5 vaccine 8.3 months after the fourth vaccination and/or experienced a breakthrough infection. Two months before and four weeks after the fifth vaccination, the live-virus neutralization capacities of Omicron variants BA.5, BQ.1.1, and XBB.1.5 were determined, as well as neutralizing and quantitative anti-SARS-CoV-2 spike-specific IgG antibodies. Four weeks after the fifth vaccination with the adapted vaccine, significantly increased neutralizing antibodies and the neutralization of Omicron variants BA.5, BQ.1.1, and XBB.1.5 were observed. The increase was significantly higher than after the fourth vaccination for variants BQ.1.1 and BA.5. Of all analyzed variants, BA.5 was neutralized best after the fifth vaccination. We did not see a difference in humoral immunity between the group with an infection and the group with a vaccination as a fifth spike exposure. Fivefold-vaccinated patients with a breakthrough infection showed a significantly higher neutralization capacity of XBB.1.5. A fifth SARS-CoV-2 vaccination with the adapted vaccine improves both wild-type specific antibody titers and the neutralizing capacity of the current Omicron variants BA.5, BQ.1.1, and XBB.1.5 in hemodialysis patients. Additional booster vaccinations with adapted vaccines will likely improve immunity towards current and original SARS-CoV-2 variants and are, therefore, recommended in hemodialysis patients. Further longitudinal studies must show the extent to which this booster vaccination avoids a breakthrough infection.

Sections du résumé

BACKGROUND BACKGROUND
Hemodialysis patients have reduced serologic immunity after SARS-CoV-2 vaccination compared to the general population and an increased risk of morbidity and mortality when exposed to SARS-CoV-2.
METHODS METHODS
Sixty-six hemodialysis patients immunized four times with the original SARS-CoV-2 vaccines (BNT162b2, mRNA-1273) either received a booster with the adapted Comirnaty Original/Omicron BA.4-5 vaccine 8.3 months after the fourth vaccination and/or experienced a breakthrough infection. Two months before and four weeks after the fifth vaccination, the live-virus neutralization capacities of Omicron variants BA.5, BQ.1.1, and XBB.1.5 were determined, as well as neutralizing and quantitative anti-SARS-CoV-2 spike-specific IgG antibodies.
RESULTS RESULTS
Four weeks after the fifth vaccination with the adapted vaccine, significantly increased neutralizing antibodies and the neutralization of Omicron variants BA.5, BQ.1.1, and XBB.1.5 were observed. The increase was significantly higher than after the fourth vaccination for variants BQ.1.1 and BA.5. Of all analyzed variants, BA.5 was neutralized best after the fifth vaccination. We did not see a difference in humoral immunity between the group with an infection and the group with a vaccination as a fifth spike exposure. Fivefold-vaccinated patients with a breakthrough infection showed a significantly higher neutralization capacity of XBB.1.5.
CONCLUSION CONCLUSIONS
A fifth SARS-CoV-2 vaccination with the adapted vaccine improves both wild-type specific antibody titers and the neutralizing capacity of the current Omicron variants BA.5, BQ.1.1, and XBB.1.5 in hemodialysis patients. Additional booster vaccinations with adapted vaccines will likely improve immunity towards current and original SARS-CoV-2 variants and are, therefore, recommended in hemodialysis patients. Further longitudinal studies must show the extent to which this booster vaccination avoids a breakthrough infection.

Identifiants

pubmed: 38543942
pii: vaccines12030308
doi: 10.3390/vaccines12030308
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : the Helmholtz Association's Initiative and Networking Fund
ID : KA1-Co-02 'COVIPA'
Organisme : the European Union's Horizon 2020 research and innovation programme
ID : no. 848223
Organisme : Netzwerk Universitätsmedizin (NUM), COVIM platform
ID : 01KX2021

Auteurs

Bo-Hung Liao (BH)

Institute of Virology, TUM School of Medicine and Health, Technical University of Munich, 81675 Munich, Germany.

Louise Platen (L)

Department of Nephrology, TUM School of Medicine and Health, University Hospital Rechts der Isar, Technical University of Munich, 81675 Munich, Germany.

Myriam Grommes (M)

Department of Nephrology, TUM School of Medicine and Health, University Hospital Rechts der Isar, Technical University of Munich, 81675 Munich, Germany.

Cho-Chin Cheng (CC)

Institute of Virology, TUM School of Medicine and Health, Technical University of Munich, 81675 Munich, Germany.

Christopher Holzmann-Littig (C)

Department of Nephrology, TUM School of Medicine and Health, University Hospital Rechts der Isar, Technical University of Munich, 81675 Munich, Germany.
TUM Medical Education Center, TUM School of Medicine and Health, Technical University of Munich, 81675 Munich, Germany.

Catharina Christa (C)

Institute of Virology, TUM School of Medicine and Health, Technical University of Munich, 81675 Munich, Germany.

Bernhard Haller (B)

Institute of AI and Informatics in Medicine, TUM School of Medicine and Health, Technical University of Munich, 81675 Munich, Germany.

Verena Kappler (V)

Department of Nephrology, TUM School of Medicine and Health, University Hospital Rechts der Isar, Technical University of Munich, 81675 Munich, Germany.

Romina Bester (R)

Institute of Virology, TUM School of Medicine and Health, Technical University of Munich, 81675 Munich, Germany.

Maia Lucia Werz (ML)

Department of Nephrology, TUM School of Medicine and Health, University Hospital Rechts der Isar, Technical University of Munich, 81675 Munich, Germany.

Eva Platen (E)

Kidney Center Eifel Dialyse, 53894 Mechernich, Germany.

Peter Eggerer (P)

KfH Kidney Center Harlaching, Munich-Harlaching, 81545 Munich, Germany.

Laëtitia Tréguer (L)

KfH Kidney Center, 83278 Traunstein, Germany.

Claudius Küchle (C)

Department of Nephrology, TUM School of Medicine and Health, University Hospital Rechts der Isar, Technical University of Munich, 81675 Munich, Germany.

Christoph Schmaderer (C)

Department of Nephrology, TUM School of Medicine and Health, University Hospital Rechts der Isar, Technical University of Munich, 81675 Munich, Germany.

Uwe Heemann (U)

Department of Nephrology, TUM School of Medicine and Health, University Hospital Rechts der Isar, Technical University of Munich, 81675 Munich, Germany.
German Center for Infection Research (DZIF), Partner Site, 81675 Munich, Germany.

Lutz Renders (L)

Department of Nephrology, TUM School of Medicine and Health, University Hospital Rechts der Isar, Technical University of Munich, 81675 Munich, Germany.
German Center for Infection Research (DZIF), Partner Site, 81675 Munich, Germany.

Ulrike Protzer (U)

Institute of Virology, TUM School of Medicine and Health, Technical University of Munich, 81675 Munich, Germany.
German Center for Infection Research (DZIF), Partner Site, 81675 Munich, Germany.
Institute of Virology, Helmholtz Munich, 85764 Munich, Germany.

Matthias Christoph Braunisch (MC)

Department of Nephrology, TUM School of Medicine and Health, University Hospital Rechts der Isar, Technical University of Munich, 81675 Munich, Germany.

Classifications MeSH