Adolescent BCG revaccination induces a phenotypic shift in CD4


Journal

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

Informations de publication

Date de publication:
18 Jun 2024
Historique:
received: 17 04 2023
accepted: 15 05 2024
medline: 19 6 2024
pubmed: 19 6 2024
entrez: 18 6 2024
Statut: epublish

Résumé

A recent clinical trial demonstrated that Bacille Calmette-Guérin (BCG) revaccination of adolescents reduced the risk of sustained infection with Mycobacterium tuberculosis (M.tb). In a companion phase 1b trial, HVTN 602/Aeras A-042, we characterize in-depth the cellular responses to BCG revaccination or to a H4:IC31 vaccine boost to identify T cell subsets that could be responsible for the protection observed. High-dimensional clustering analysis of cells profiled using a 26-color flow cytometric panel show marked increases in five effector memory CD4

Identifiants

pubmed: 38890283
doi: 10.1038/s41467-024-49050-1
pii: 10.1038/s41467-024-49050-1
doi:

Substances chimiques

BCG Vaccine 0

Types de publication

Journal Article Clinical Trial, Phase I

Langues

eng

Sous-ensembles de citation

IM

Pagination

5191

Subventions

Organisme : U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID)
ID : UM1AI068618
Organisme : U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID)
ID : UM1AI068635

Informations de copyright

© 2024. The Author(s).

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Auteurs

One B Dintwe (OB)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Cape Town HVTN Immunology Laboratory, Hutchinson Centre Research Institute of South Africa, Cape Town, South Africa.

Lamar Ballweber Fleming (L)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.

Valentin Voillet (V)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Cape Town HVTN Immunology Laboratory, Hutchinson Centre Research Institute of South Africa, Cape Town, South Africa.

John McNevin (J)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.

Aaron Seese (A)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.

Anneta Naidoo (A)

Cape Town HVTN Immunology Laboratory, Hutchinson Centre Research Institute of South Africa, Cape Town, South Africa.

Saleha Omarjee (S)

Cape Town HVTN Immunology Laboratory, Hutchinson Centre Research Institute of South Africa, Cape Town, South Africa.

Linda-Gail Bekker (LG)

The Desmond Tutu HIV Centre, Institute of Infectious Diseases and Molecular Medicine, University of Cape Town, Cape Town, South Africa.

James G Kublin (JG)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.

Stephen C De Rosa (SC)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA, USA.

Evan W Newell (EW)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.

Andrew Fiore-Gartland (A)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.

Erica Andersen-Nissen (E)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA. eanderse@hcrisa.org.za.
Cape Town HVTN Immunology Laboratory, Hutchinson Centre Research Institute of South Africa, Cape Town, South Africa. eanderse@hcrisa.org.za.

M Juliana McElrath (MJ)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA. jmcelrat@fredhutch.org.
Department of Medicine, University of Washington School of Medicine, Seattle, WA, USA. jmcelrat@fredhutch.org.

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