SARS-CoV-2 live virus neutralization after four COVID-19 vaccine doses in people with HIV receiving suppressive antiretroviral therapy.


Journal

AIDS (London, England)
ISSN: 1473-5571
Titre abrégé: AIDS
Pays: England
ID NLM: 8710219

Informations de publication

Date de publication:
01 04 2023
Historique:
pubmed: 16 2 2023
medline: 17 3 2023
entrez: 15 2 2023
Statut: ppublish

Résumé

Limited data exist regarding the immune benefits of fourth COVID-19 vaccine doses in people with HIV (PWH) receiving antiretroviral therapy (ART), particularly now that most have experienced a SARS-CoV-2 infection. We quantified wild-type, Omicron-BA.5 and Omicron-BQ.1-specific neutralization up to 1 month post-fourth COVID-19 vaccine dose in 63 (19 SARS-CoV-2-naive and 44 SARS-CoV-2-experienced) PWH. A longitudinal observational cohort. Quantification of wild-type-, Omicron-BA.5, and Omicron-BQ.1-specific neutralization using live virus assays. Participants received monovalent (44%) and bivalent (56%) mRNA fourth doses. In COVID-19-naive PWH, fourth doses enhanced wild-type and Omicron-BA.5-specific neutralization modestly above three-dose levels ( P  = 0.1). In COVID-19-experienced PWH, fourth doses enhanced wild-type specific neutralization modestly ( P  = 0.1) and BA.5-specific neutralization substantially ( P  = 0.002). Consistent with humoral benefits of 'hybrid' immunity, COVID-19-experienced PWH exhibited the highest neutralization post-fourth dose, wherein those with Omicron-era infections displayed higher wild-type specific ( P  = 0.04) but similar BA.5 and BQ.1-specific neutralization than those with pre-Omicron-era infections. Nevertheless, BA.5-specific neutralization was significantly below wild-type in everyone regardless of COVID-19 experience, with BQ.1-specific neutralization lower still (both P  < 0.0001). In multivariable analyses, fourth dose valency did not affect neutralization magnitude. Rather, an mRNA-1273 fourth dose (versus a BNT162b2 one) was the strongest correlate of wild-type specific neutralization, while prior COVID-19, regardless of pandemic era, was the strongest correlate of BA.5 and BQ.1-specific neutralization post-fourth dose. Fourth COVID-19 vaccine doses, irrespective of valency, benefit PWH regardless of prior SARS-CoV-2 infection. Results support recommendations that all adults receive a fourth COVID-19 vaccine dose within 6 months of their third dose (or their most recent SARS-CoV-2 infection).

Identifiants

pubmed: 36789806
doi: 10.1097/QAD.0000000000003519
pii: 00002030-202304010-00001
pmc: PMC9994812
doi:

Substances chimiques

Antibodies, Neutralizing 0
Antibodies, Viral 0
BNT162 Vaccine 0
COVID-19 Vaccines 0

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

F11-F18

Subventions

Organisme : CIHR
ID : GA2–177713
Pays : Canada

Informations de copyright

Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc.

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Auteurs

Peter K Cheung (PK)

British Columbia Centre for Excellence in HIV/AIDS, Vancouver.
Faculty of Health Sciences, Simon Fraser University, Burnaby.

Hope R Lapointe (HR)

British Columbia Centre for Excellence in HIV/AIDS, Vancouver.

Yurou Sang (Y)

Faculty of Health Sciences, Simon Fraser University, Burnaby.

Siobhan Ennis (S)

Faculty of Health Sciences, Simon Fraser University, Burnaby.

Francis Mwimanzi (F)

Faculty of Health Sciences, Simon Fraser University, Burnaby.

Sarah Speckmaier (S)

British Columbia Centre for Excellence in HIV/AIDS, Vancouver.

Evan Barad (E)

British Columbia Centre for Excellence in HIV/AIDS, Vancouver.
Faculty of Health Sciences, Simon Fraser University, Burnaby.

Winnie Dong (W)

British Columbia Centre for Excellence in HIV/AIDS, Vancouver.

Richard Liang (R)

British Columbia Centre for Excellence in HIV/AIDS, Vancouver.

Janet Simons (J)

Department of Pathology and Laboratory Medicine, Providence Healthcare.
Department of Pathology and Laboratory Medicine, University of British Columbia.

Christopher F Lowe (CF)

Department of Pathology and Laboratory Medicine, Providence Healthcare.
Department of Pathology and Laboratory Medicine, University of British Columbia.
Division of Medical Microbiology and Virology, St. Paul's Hospital.

Marc G Romney (MG)

Department of Pathology and Laboratory Medicine, Providence Healthcare.
Department of Pathology and Laboratory Medicine, University of British Columbia.
Division of Medical Microbiology and Virology, St. Paul's Hospital.

Chanson J Brumme (CJ)

British Columbia Centre for Excellence in HIV/AIDS, Vancouver.
Department of Medicine, University of British Columbia, Vancouver.

Masahiro Niikura (M)

Faculty of Health Sciences, Simon Fraser University, Burnaby.

Mark A Brockman (MA)

British Columbia Centre for Excellence in HIV/AIDS, Vancouver.
Faculty of Health Sciences, Simon Fraser University, Burnaby.
Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, British Columbia, Canada.

Zabrina L Brumme (ZL)

British Columbia Centre for Excellence in HIV/AIDS, Vancouver.
Faculty of Health Sciences, Simon Fraser University, Burnaby.

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