Boosting BCG with proteins or rAd5 does not enhance protection against tuberculosis in rhesus macaques.

Diseases Immunology Microbiology

Journal

NPJ vaccines
ISSN: 2059-0105
Titre abrégé: NPJ Vaccines
Pays: England
ID NLM: 101699863

Informations de publication

Date de publication:
2019
Historique:
received: 03 01 2019
accepted: 03 05 2019
entrez: 1 6 2019
pubmed: 1 6 2019
medline: 1 6 2019
Statut: epublish

Résumé

Tuberculosis (TB) is the leading cause of death from infection worldwide. The only approved vaccine, BCG, has variable protective efficacy against pulmonary TB, the transmissible form of the disease. Therefore, improving this efficacy is an urgent priority. This study assessed whether heterologous prime-boost vaccine regimens in which BCG priming is boosted with either (i) protein and adjuvant (M72 plus AS01

Identifiants

pubmed: 31149352
doi: 10.1038/s41541-019-0113-9
pii: 113
pmc: PMC6538611
doi:

Types de publication

Journal Article

Langues

eng

Pagination

21

Déclaration de conflit d'intérêts

Competing interestsThe authors from University of Pittsburgh, NIH and Aeras have no competing interests. At Statens Serum Institut, Peter Andersen is a coinventor of patents relating to cationic liposomes as vaccine adjuvants and of patents relating to TB fusion protein Ag85B-ESAT-6-Rv2660 (H56). All rights have been assigned to Statens Serum Institut (SSI).

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Auteurs

Patricia A Darrah (PA)

1Vaccine Research Center, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD USA.

Robert M DiFazio (RM)

2Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA USA.

Pauline Maiello (P)

2Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA USA.

Hannah P Gideon (HP)

2Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA USA.

Amy J Myers (AJ)

2Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA USA.

Mark A Rodgers (MA)

2Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA USA.

Joshua A Hackney (JA)

1Vaccine Research Center, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD USA.

Thomas Lindenstrom (T)

3Center for Vaccine Research, Statens Serum Institut, Copenhagen, Denmark.

Thomas Evans (T)

4Aeras, Rockville, MD USA.

Charles A Scanga (CA)

2Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA USA.

Victor Prikhodko (V)

4Aeras, Rockville, MD USA.

Peter Andersen (P)

3Center for Vaccine Research, Statens Serum Institut, Copenhagen, Denmark.

Philana Ling Lin (PL)

5Department of Pediatrics, Children's Hospital of the University of Pittsburgh of UPMC, Pittsburgh, PA USA.

Dominick Laddy (D)

4Aeras, Rockville, MD USA.

Mario Roederer (M)

1Vaccine Research Center, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD USA.

Robert A Seder (RA)

1Vaccine Research Center, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD USA.

JoAnne L Flynn (JL)

2Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA USA.

Classifications MeSH