A Multivariant Surrogate Virus Neutralization Test Demonstrates Distinct SARS-CoV-2-Specific Antibody Responses in People Living with HIV after a Fourth Monovalent mRNA Vaccination or an Omicron Breakthrough Infection.

Omicron PLWH SARS-CoV-2 antibodies neutralization surrogate vaccination

Journal

Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402

Informations de publication

Date de publication:
16 Apr 2024
Historique:
received: 23 02 2024
revised: 30 03 2024
accepted: 11 04 2024
medline: 26 4 2024
pubmed: 26 4 2024
entrez: 26 4 2024
Statut: epublish

Résumé

While neutralizing antibodies (nAbs) induced by monovalent severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccinations are primarily directed against the wildtype (WT), subsequent exposure to the Omicron variants may increase the breadth of the antibodies' cross-neutralizing activity. Here, we analyzed the impact of an Omicron breakthrough infection (BTI) or a fourth monovalent mRNA vaccination on nAb profiles in people living with human immunodeficiency virus (PLWH). Using a multivariant surrogate virus neutralization test (sVNT), we quantified nAbs in 36 three-times vaccinated PLWH, of whom 9 acquired a serologically confirmed Omicron BTI, 8 received a fourth vaccine dose, and 19 were neither infected nor additionally vaccinated. While nAbs against WT and Delta increased after the BTI and a fourth vaccination, a significant increase against BA.1, BA.2, and BA.5 was only observed after the BTI. However, there was no significant difference in nAb concentrations between the samples obtained after the BTI and fourth vaccination. In contrast, nAb levels were significantly lower in PLWH, who were neither infected nor additionally vaccinated after three vaccinations. Thus, our study demonstrates the suitability of a multivariant sVNT to assess hybrid humoral immunity after Omicron BTIs in PLWH vaccinated against SARS-CoV-2.

Identifiants

pubmed: 38667468
pii: diagnostics14080822
doi: 10.3390/diagnostics14080822
pii:
doi:

Types de publication

Journal Article

Langues

eng

Déclaration de conflit d'intérêts

The authors declare no conflicts of interest.

Auteurs

David Niklas Springer (DN)

Center for Virology, Medical University of Vienna, 1090 Vienna, Austria.

Simon Daller (S)

Department of Respiratory and Pulmonary Diseases, Vienna Healthcare Group, Clinic Penzing, 1140 Vienna, Austria.

Michael Knappik (M)

Department of Respiratory and Pulmonary Diseases, Vienna Healthcare Group, Clinic Penzing, 1140 Vienna, Austria.

Katja Prüger (K)

Center for Virology, Medical University of Vienna, 1090 Vienna, Austria.

Sylvia Hartl (S)

Department of Respiratory and Pulmonary Diseases, Vienna Healthcare Group, Clinic Penzing, 1140 Vienna, Austria.
Ludwig Boltzmann Institute for Lung Health, 1140 Vienna, Austria.
Faculty of Medicine, Sigmund Freud University, 1020 Vienna, Austria.

Robab Breyer-Kohansal (R)

Department of Respiratory and Pulmonary Diseases, Vienna Healthcare Group, Clinic Penzing, 1140 Vienna, Austria.
Ludwig Boltzmann Institute for Lung Health, 1140 Vienna, Austria.

Elisabeth Puchhammer-Stöckl (E)

Center for Virology, Medical University of Vienna, 1090 Vienna, Austria.

Judith Helene Aberle (JH)

Center for Virology, Medical University of Vienna, 1090 Vienna, Austria.

Lukas Weseslindtner (L)

Center for Virology, Medical University of Vienna, 1090 Vienna, Austria.

Marie Kathrin Breyer (MK)

Department of Respiratory and Pulmonary Diseases, Vienna Healthcare Group, Clinic Penzing, 1140 Vienna, Austria.
Ludwig Boltzmann Institute for Lung Health, 1140 Vienna, Austria.

Classifications MeSH