Memory B cell responses induced by pneumococcal conjugate vaccine schedules with fewer doses: analysis of a randomised-controlled trial in Viet Nam.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
14 Aug 2024
Historique:
received: 27 05 2024
accepted: 06 08 2024
medline: 14 8 2024
pubmed: 14 8 2024
entrez: 13 8 2024
Statut: epublish

Résumé

The use of pneumococcal conjugate vaccine (PCV) schedules with fewer doses are being considered to reduce costs and improve access, particularly in low- and middle-income countries. While several studies have assessed their immunogenicity, there are limited data on their potential for long-term immune protection, as assessed by pneumococcal serotype-specific memory B cell (B

Identifiants

pubmed: 39138203
doi: 10.1038/s41467-024-51413-7
pii: 10.1038/s41467-024-51413-7
doi:

Substances chimiques

Pneumococcal Vaccines 0
13-valent pneumococcal vaccine 0
Vaccines, Conjugate 0
Antibodies, Bacterial 0
10-valent pneumococcal conjugate vaccine 0
Immunoglobulin G 0

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

6968

Subventions

Organisme : Bill & Melinda Gates Foundation
ID : INV-008627
Pays : United States

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Darren Suryawijaya Ong (DS)

Infection, Immunity & Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.

Thanh V Phan (TV)

Pasteur Institute of Ho Chi Minh City, Ho Chi Minh City, Viet Nam.

Beth Temple (B)

Infection, Immunity & Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Menzies School of Health Research, Charles Darwin University, Darwin, NT, Australia.
Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, United Kingdom.

Zheng Quan Toh (ZQ)

Infection, Immunity & Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.

Cattram Duong Nguyen (CD)

Infection, Immunity & Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.

Kien Vientrung (K)

Pasteur Institute of Ho Chi Minh City, Ho Chi Minh City, Viet Nam.

Hoang Van Anh Nguyen (HVA)

Pasteur Institute of Ho Chi Minh City, Ho Chi Minh City, Viet Nam.

Vo Thi Trang Dai (V)

Pasteur Institute of Ho Chi Minh City, Ho Chi Minh City, Viet Nam.

Kathryn Bright (K)

Infection, Immunity & Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.

Hau Phuc Tran (HP)

Pasteur Institute of Ho Chi Minh City, Ho Chi Minh City, Viet Nam.

Rachel Ann Higgins (RA)

Infection, Immunity & Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.

Yin Bun Cheung (YB)

Centre for Quantitative Medicine and Program in Health Services & Systems Research, Duke-NUS Medical School, Singapore, Singapore.
Tampere Center for Child, Adolescent and Maternal Health Research, Tampere University, Tampere, Finland.

Thuong Vu Nguyen (T)

Pasteur Institute of Ho Chi Minh City, Ho Chi Minh City, Viet Nam.

Kim Mulholland (K)

Infection, Immunity & Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.
Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, United Kingdom.

Paul Vincent Licciardi (PV)

Infection, Immunity & Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia. paul.licciardi@mcri.edu.au.
Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia. paul.licciardi@mcri.edu.au.

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