Replication-Competent NYVAC-KC Yields Improved Immunogenicity to HIV-1 Antigens in Rhesus Macaques Compared to Nonreplicating NYVAC.


Journal

Journal of virology
ISSN: 1098-5514
Titre abrégé: J Virol
Pays: United States
ID NLM: 0113724

Informations de publication

Date de publication:
01 02 2019
Historique:
received: 13 09 2018
accepted: 31 10 2018
pubmed: 16 11 2018
medline: 9 11 2019
entrez: 16 11 2018
Statut: epublish

Résumé

As part of the continuing effort to develop an effective HIV vaccine, we generated a poxviral vaccine vector (previously described) designed to improve on the results of the RV144 phase III clinical trial. The construct, NYVAC-KC, is a replication-competent, attenuated recombinant of the vaccinia virus strain NYVAC. NYVAC is a vector that has been used in many previous clinical studies but is replication deficient. Here, we report a side-by-side comparison of replication-restricted NYVAC and replication-competent NYVAC-KC in a nonhuman primate study, which utilized a prime-boost regimen similar to that of RV144. NYVAC-C and NYVAC-C-KC express the HIV-1 antigens gp140, and Gag/Gag-Pol-Nef-derived virus-like particles (VLPs) from clade C and were used as the prime, with recombinant virus plus envelope protein used as the boost. In nearly every T and B cell immune assay against HIV-1, including neutralization and antibody binding, NYVAC-C-KC induced a greater immune response than NYVAC-C, indicating that replication competence in a poxvirus may improve upon the modestly successful regimen used in the RV144 clinical trial.

Identifiants

pubmed: 30429340
pii: JVI.01513-18
doi: 10.1128/JVI.01513-18
pmc: PMC6340019
pii:
doi:

Substances chimiques

Antibodies, Neutralizing 0
HIV Antibodies 0
HIV Antigens 0
NYVAC vaccine 0
Viral Vaccines 0
env Gene Products, Human Immunodeficiency Virus 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI118581
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001414
Pays : United States

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2019 American Society for Microbiology.

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Auteurs

Karen V Kibler (KV)

Biodesign Institute, Arizona State University, Tempe, Arizona, USA.

Benedikt Asbach (B)

Institute of Medical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany.

Beatriz Perdiguero (B)

Department of Molecular and Cellular Biology, Centro Nacional de Biotecnología, Consejo Superior de Investigaciones Científicas, Madrid, Spain.

Juan García-Arriaza (J)

Department of Molecular and Cellular Biology, Centro Nacional de Biotecnología, Consejo Superior de Investigaciones Científicas, Madrid, Spain.

Nicole L Yates (NL)

Duke University Medical Center, Durham, North Carolina, USA.

Robert Parks (R)

Duke University Medical Center, Durham, North Carolina, USA.

Sherry Stanfield-Oakley (S)

Duke University Medical Center, Durham, North Carolina, USA.

Guido Ferrari (G)

Duke University Medical Center, Durham, North Carolina, USA.

David C Montefiori (DC)

Duke University Medical Center, Durham, North Carolina, USA.

Georgia D Tomaras (GD)

Duke University Medical Center, Durham, North Carolina, USA.

Mario Roederer (M)

Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.

Kathryn E Foulds (KE)

Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.

Donald N Forthal (DN)

Division of Infectious Diseases Department of Medicine, University of California, Irvine School of Medicine, Irvine, California, USA.

Michael S Seaman (MS)

Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.

Steve Self (S)

Statistical Center for HIV/AIDS Research and Prevention, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.

Raphael Gottardo (R)

Statistical Center for HIV/AIDS Research and Prevention, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.

Sanjay Phogat (S)

Sanofi Pasteur, Swiftwater, Pennsylvania, USA.

James Tartaglia (J)

Sanofi Pasteur, Swiftwater, Pennsylvania, USA.

Susan Barnett (S)

Novartis Vaccines and Diagnostics, Inc., Cambridge, Massachusetts, USA.

Anthony D Cristillo (AD)

Advanced BioScience Laboratories, Inc., Rockville, Maryland, USA.

Deborah Weiss (D)

Advanced BioScience Laboratories, Inc., Rockville, Maryland, USA.

Lindsey Galmin (L)

Advanced BioScience Laboratories, Inc., Rockville, Maryland, USA.

Song Ding (S)

EuroVacc Foundation, Lausanne, Switzerland.

Jonathan L Heeney (JL)

Lab of Viral Zoonotics, Department of Veterinary Medicine, University of Cambridge, Cambridge, United Kingdom.

Mariano Esteban (M)

Department of Molecular and Cellular Biology, Centro Nacional de Biotecnología, Consejo Superior de Investigaciones Científicas, Madrid, Spain.

Ralf Wagner (R)

Institute of Medical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany.
Institute of Clinical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany.

Giuseppe Pantaleo (G)

Division of Immunology and Allergy, Department of Medicine, Centre Hospitalier Universitaire Vaudois, University of Lausanne, Lausanne, Switzerland.

Bertram L Jacobs (BL)

Biodesign Institute, Arizona State University, Tempe, Arizona, USA bjacobs@asu.edu.
School of Life Sciences, Arizona State University, Tempe, Arizona, USA.

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