Replication-Competent NYVAC-KC Yields Improved Immunogenicity to HIV-1 Antigens in Rhesus Macaques Compared to Nonreplicating NYVAC.
Animals
Antibodies, Neutralizing
/ blood
CD4-Positive T-Lymphocytes
/ immunology
HIV Antibodies
/ blood
HIV Antigens
/ immunology
HIV Infections
/ immunology
HIV-1
/ immunology
Humans
Macaca mulatta
Male
Vaccination
Vaccinia virus
/ immunology
Viral Vaccines
/ administration & dosage
Virus Replication
env Gene Products, Human Immunodeficiency Virus
/ immunology
Gag-Pol-Nef
HIV
NYVAC
NYVAC-KC
T cell response
antibody responses
gp140
nonhuman primates
vaccines
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
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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