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HIV vaccine candidate activation of hypoxia and the inflammasome in CD14+ monocytes is associated with a decreased risk of SIVmac251 acquisition.

Abstract
Qualitative differences in the innate and adaptive responses elicited by different HIV vaccine candidates have not been thoroughly investigated. We tested the ability of the Aventis Pasteur live recombinant canarypox vector (ALVAC)-SIV, DNA-SIV and Ad26-SIV vaccine prime modalities together with two ALVAC-SIV + gp120 protein boosts to reduce the risk of SIVmac251 acquisition in rhesus macaques. We found that the DNA and ALVAC prime regimens were effective, but the Ad26 prime was not. The activation of hypoxia and the inflammasome in CD14+CD16- monocytes, gut-homing CCR5-negative CD4+ T helper 2 (TH2) cells and antibodies to variable region 2 correlated with a decreased risk of SIVmac251 acquisition. By contrast, signal transducer and activator of transcription 3 activation in CD16+ monocytes was associated with an increased risk of virus acquisition. The Ad26 prime regimen induced the accumulation of CX3CR1+CD163+ macrophages in lymph nodes and of long-lasting CD4+ TH17 cells in the gut and lungs. Our data indicate that the selective engagement of monocyte subsets following a vaccine prime influences long-term immunity, uncovering an unexpected association of CD14+ innate monocytes with a reduced risk of SIVmac251 acquisition.
AuthorsMonica Vaccari, Slim Fourati, Shari N Gordon, Dallas R Brown, Massimilano Bissa, Luca Schifanella, Isabela Silva de Castro, Melvin N Doster, Veronica Galli, Maria Omsland, Dai Fujikawa, Giacomo Gorini, Namal P M Liyanage, Hung V Trinh, Katherine M McKinnon, Kathryn E Foulds, Brandon F Keele, Mario Roederer, Richard A Koup, Xiaoying Shen, Georgia D Tomaras, Marcus P Wong, Karissa J Munoz, Johannes S Gach, Donald N Forthal, David C Montefiori, David J Venzon, Barbara K Felber, Margherita Rosati, George N Pavlakis, Mangala Rao, Rafick-Pierre Sekaly, Genoveffa Franchini
JournalNature medicine (Nat Med) Vol. 24 Issue 6 Pg. 847-856 (06 2018) ISSN: 1546-170X [Electronic] United States
PMID29785023 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
Chemical References
  • AIDS Vaccines
  • Biomarkers
  • Inflammasomes
  • Lipopolysaccharide Receptors
  • Receptors, CCR5
  • Vaccines, DNA
Topics
  • AIDS Vaccines (immunology)
  • Animals
  • Antibody Formation (immunology)
  • Biomarkers (metabolism)
  • CD4-Positive T-Lymphocytes (immunology)
  • Hypoxia (immunology)
  • Inflammasomes (metabolism)
  • Inflammation (pathology)
  • Killer Cells, Natural (immunology)
  • Lipopolysaccharide Receptors (metabolism)
  • Macaca mulatta
  • Monocytes (pathology)
  • Receptors, CCR5 (metabolism)
  • Risk Factors
  • Simian Immunodeficiency Virus (physiology)
  • T-Lymphocytes, Helper-Inducer (immunology)
  • Vaccines, DNA (immunology)

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