Evidence map›Paper›PMID 27077384›Full record

ArticlePloS one2016

Targeting HIV-1 Env gp140 to LOX-1 Elicits Immune Responses in Rhesus Macaques.

Gerard Zurawski, Sandra Zurawski, Anne-Laure Flamar, Laura Richert, Ralf Wagner, Georgia D Tomaras, David C Montefiori, Mario Roederer, Guido Ferrari, Christine Lacabaratz and 21 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

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  10. [Vaccine of the future].Revue francophone des laboratoires : RFL · 2019
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

31 authors at 11 institutions in 4 countries.

Gerard ZurawskiVaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, and Assistance Publique-Hôpitaux de Paris, Groupe Henri-Mondor Albert- Chenevier, service d'immunologie clinique, INRIA SISTM, Créteil, France.ORCID http://orcid.org/0000-0002-0168-3523
Sandra ZurawskiVaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, and Assistance Publique-Hôpitaux de Paris, Groupe Henri-Mondor Albert- Chenevier, service d'immunologie clinique, INRIA SISTM, Créteil, France.
Anne-Laure FlamarVaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, and Assistance Publique-Hôpitaux de Paris, Groupe Henri-Mondor Albert- Chenevier, service d'immunologie clinique, INRIA SISTM, Créteil, France.
Laura RichertINSERM U897, INRIA SISTM, Université Bordeaux Segalen, Bordeaux, France.
Ralf WagnerMolecular Microbiology and Gene Therapy Unit, Institute of Medical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany.
Georgia D TomarasDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, United States of America.
David C MontefioriDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, United States of America.
Mario RoedererVaccine Research Center, NIAID, NIH, Bethesda, Maryland, United States of America.
Guido FerrariDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, United States of America.
Christine LacabaratzVaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, and Assistance Publique-Hôpitaux de Paris, Groupe Henri-Mondor Albert- Chenevier, service d'immunologie clinique, INRIA SISTM, Créteil, France.
Henri BonnabauINSERM U897, INRIA SISTM, Université Bordeaux Segalen, Bordeaux, France.
Peter KlucarVaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, and Assistance Publique-Hôpitaux de Paris, Groupe Henri-Mondor Albert- Chenevier, service d'immunologie clinique, INRIA SISTM, Créteil, France.
Zhiqing WangVaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, and Assistance Publique-Hôpitaux de Paris, Groupe Henri-Mondor Albert- Chenevier, service d'immunologie clinique, INRIA SISTM, Créteil, France.
Kathryn E FouldsVaccine Research Center, NIAID, NIH, Bethesda, Maryland, United States of America.
Shing-Fen KaoVaccine Research Center, NIAID, NIH, Bethesda, Maryland, United States of America.
Nicole L YatesDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, United States of America.
Celia LaBrancheDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, United States of America.
Bertram L JacobsSchool of Life Sciences, Center for Infectious Diseases and Vaccinology, Arizona State University, Tempe, Arizona, United States of America.
Karen KiblerSchool of Life Sciences, Center for Infectious Diseases and Vaccinology, Arizona State University, Tempe, Arizona, United States of America.
Benedikt AsbachMolecular Microbiology and Gene Therapy Unit, Institute of Medical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany.
Alexander KlicheMolecular Microbiology and Gene Therapy Unit, Institute of Medical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany.
Andres SalazarOncovir, Washington, D.C., United States of America.
Steve ReedInfectious Disease Research Institute, Seattle, Washington, United States of America.
Steve SelfVaccine and Infectious Disease and Public Health Sciences Divisions, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Raphael GottardoVaccine and Infectious Disease and Public Health Sciences Divisions, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Lindsey GalminAdvanced BioScience Laboratories, Inc., Rockville, Maryland, United States of America.
Deborah WeissAdvanced BioScience Laboratories, Inc., Rockville, Maryland, United States of America.
Anthony CristilloAdvanced BioScience Laboratories, Inc., Rockville, Maryland, United States of America.
Rodolphe ThiebautINSERM U897, INRIA SISTM, Université Bordeaux Segalen, Bordeaux, France.
Giuseppe PantaleoCentre Hospitalier Universitaire Vaudois, CH-101, Lausanne, Switzerland.
Yves LevyVaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, and Assistance Publique-Hôpitaux de Paris, Groupe Henri-Mondor Albert- Chenevier, service d'immunologie clinique, INRIA SISTM, Créteil, France.
Inserm · FRDuke Medical Center · USBioScience Laboratories (United States) · USInstitute of Medical Microbiology and Hygiene · DEInstitut national de recherche en sciences et technologies du numérique · FRNational Institutes of Health · USArizona State University · USFred Hutch Cancer Center · USInfectious Disease Research Institute · USOncovir (United States) · USUniversity Hospital of Lausanne · CH

Funding

Non-Human Primate CoreZICAI005103 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI FOULDS, KATHRYN · 2009 to 2025
$22.7M
Functional And Phenotypic Characterization Of T Cells In ManZIAAI005021 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI ROEDERER, MARIO · 2009 to 2022
$14.4M
Development Of Flow Cytometric Technologies For Immune AssaysZIAAI005020 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI ROEDERER, MARIO · 2009 to 2019
$9.6M
6 · The paper itself

Abstract

Improved antigenicity against HIV-1 envelope (Env) protein is needed to elicit vaccine-induced protective immunity in humans. Here we describe the first tests in non-human primates (NHPs) of Env gp140 protein fused to a humanized anti-LOX-1 recombinant antibody for delivering Env directly to LOX-1-bearing antigen presenting cells, especially dendritic cells (DC). LOX-1, or 1ectin-like oxidized low-density lipoprotein (LDL) receptor-1, is expressed on various antigen presenting cells and endothelial cells, and is involved in promoting humoral immune responses. The anti-LOX-1 Env gp140 fusion protein was tested for priming immune responses and boosting responses in animals primed with replication competent NYVAC-KC Env gp140 vaccinia virus. Anti-LOX-1 Env gp140 vaccination elicited robust cellular and humoral responses when used for either priming or boosting immunity. Co-administration with Poly ICLC, a TLR3 agonist, was superior to GLA, a TLR4 agonist. Both CD4+ and CD8+ Env-specific T cell responses were elicited by anti-LOX-1 Env gp140, but in particular the CD4+ T cells were multifunctional and directed to multiple epitopes. Serum IgG and IgA antibody responses induced by anti-LOX-1 Env gp140 against various gp140 domains were cross-reactive across HIV-1 clades; however, the sera neutralized only HIV-1 bearing sequences most similar to the clade C 96ZM651 Env gp140 carried by the anti-LOX-1 vehicle. These data, as well as the safety of this protein vaccine, justify further exploration of this DC-targeting vaccine approach for protective immunity against HIV-1.

Indexed as

AIDS VaccinesAnimalsAntibodies, Monoclonal, HumanizedAntibodies, ViralAntibody Specificityenv Gene Products, Human Immunodeficiency VirusHIV-1HumansMacaca mulattaMaleMiceRecombinant Fusion ProteinsScavenger Receptors, Class ET-LymphocytesAIDS VaccinesAntibodies, Monoclonal, HumanizedAntibodies, Viralenv Gene Products, Human Immunodeficiency Virusgp140 envelope protein, Human immunodeficiency virus 1OLR1 protein, humanRecombinant Fusion ProteinsScavenger Receptors, Class E

Identifiers

PMID27077384
PMCPMC4831750
OpenAlexW2340622963

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.