MPXV Infection Stimulates a More Robust and Durable Neutralizing Antibody Response Compared to MVA-BN Vaccination.

humoral immunity mpox orthopoxviruses vaccine response

Journal

The Journal of infectious diseases
ISSN: 1537-6613
Titre abrégé: J Infect Dis
Pays: United States
ID NLM: 0413675

Informations de publication

Date de publication:
18 Oct 2024
Historique:
received: 10 07 2024
revised: 18 09 2024
accepted: 16 10 2024
medline: 18 10 2024
pubmed: 18 10 2024
entrez: 18 10 2024
Statut: aheadofprint

Résumé

Monkeypox virus (MPXV) has recently caused a global disease outbreak in humans. Differences in the neutralizing antibody response to vaccination vs. MPXV infection remain poorly understood. Here, we examined the neutralization of MPXV and VACV by sera from a cohort of convalescent and vaccinated individuals at 1- and 8-months post-exposure. Convalescent individuals displayed higher neutralizing antibody titers against MPXV than vaccinated and MPXV-naïve persons at one-month post-exposure. Neutralizing antibody titers had waned significantly in both groups at 8 months. This study suggests additional vaccine strategies are needed to elicit a durable humoral response and prevent breakthrough infections.

Identifiants

pubmed: 39422181
pii: 7826114
doi: 10.1093/infdis/jiae515
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

Auteurs

Christopher N Selverian (CN)

Albert Einstein College of Medicine, Department of Microbiology and Immunology, Bronx, NY, USA.

Stephanie R Monticelli (SR)

Viral Immunology Branch, Virology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, USA.
The Geneva Foundation, Tacoma WA, USA.

Yakin M Jaleta (YM)

Albert Einstein College of Medicine, Department of Microbiology and Immunology, Bronx, NY, USA.

Gorka Lasso (G)

Albert Einstein College of Medicine, Department of Microbiology and Immunology, Bronx, NY, USA.

Megan E DeMouth (ME)

Albert Einstein College of Medicine, Department of Microbiology and Immunology, Bronx, NY, USA.

Annalisa Meola (A)

G5 Structural Biology of Infectious Diseases, Institut Pasteur, Université Paris Cité, Paris, France.

Jacob Berrigan (J)

Albert Einstein College of Medicine, Department of Microbiology and Immunology, Bronx, NY, USA.

Thomas G Batchelor (TG)

Viral Immunology Branch, Virology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, USA.
Oak Ridge Institute of Science and Education, Oak Ridge, TN, USA.

Leandro Battini (L)

G5 Structural Biology of Infectious Diseases, Institut Pasteur, Université Paris Cité, Paris, France.

Pablo Guardado-Calvo (P)

G5 Structural Biology of Infectious Diseases, Institut Pasteur, Université Paris Cité, Paris, France.

Andrew S Herbert (AS)

Viral Immunology Branch, Virology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, USA.

Kartik Chandran (K)

Albert Einstein College of Medicine, Department of Microbiology and Immunology, Bronx, NY, USA.

Eric Meyerowitz (E)

Division of Infectious Diseases, Montefiore Medical Center, Bronx, NY, USA.
Albert Einstein College of Medicine, Department of Medicine, Bronx, NY, USA.

Emily Happy Miller (EH)

Albert Einstein College of Medicine, Department of Microbiology and Immunology, Bronx, NY, USA.
Albert Einstein College of Medicine, Department of Medicine, Bronx, NY, USA.

Classifications MeSH