Evidence map›Paper›PMID 28202751›Full record

ArticleJournal of virology2017

Superiority in Rhesus Macaques of Targeting HIV-1 Env gp140 to CD40 versus LOX-1 in Combination with Replication-Competent NYVAC-KC for Induction of Env-Specific Antibody and T Cell Responses.

Gerard Zurawski, Xiaoying Shen, Sandra Zurawski, Georgia D Tomaras, David C Montefiori, Mario Roederer, Guido Ferrari, Christine Lacabaratz, Peter Klucar, Zhiqing Wang and 18 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

26 citing papers in PubMed, 36 citations in OpenAlex.

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  14. Anti-CD40 Antibodies Fused to CD40 Ligand Have Superagonist Properties.Journal of immunology (Baltimore, Md. : 1950) · 2021
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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

28 authors at 10 institutions in 3 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, Créteil, France.
Xiaoying ShenDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
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, Créteil, France.
Georgia D TomarasDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
David C MontefioriDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, USA.
Mario RoedererVaccine Research Center, NIAID, NIH, Bethesda, Maryland, USA.
Guido FerrariDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, USA.
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, Créteil, 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, 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, Créteil, France.
Kathryn E FouldsVaccine Research Center, NIAID, NIH, Bethesda, Maryland, USA.
Shing-Fen KaoVaccine Research Center, NIAID, NIH, Bethesda, Maryland, USA.
Xuesong YuStatistical Center for HIV/AIDS Research and Prevention, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Alicia SatoStatistical Center for HIV/AIDS Research and Prevention, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Nicole L YatesDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Celia LaBrancheDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, USA.
Sherry Stanfield-OakleyDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, USA.
Karen KiblerSchool of Life Sciences, Center for Infectious Diseases and Vaccinology, Arizona State University, Tempe, Arizona, USA.
Bertram JacobsSchool of Life Sciences, Center for Infectious Diseases and Vaccinology, Arizona State University, Tempe, Arizona, USA.
Andres SalazarOncovir, Washington, DC, USA.
Steve SelfVaccine and Infectious Disease and Public Health Sciences Divisions, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
William FulpVaccine and Infectious Disease and Public Health Sciences Divisions, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Raphael GottardoVaccine and Infectious Disease and Public Health Sciences Divisions, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Lindsey GalminAdvanced BioScience Laboratories, Inc., Rockville, Maryland, USA.
Deborah WeissAdvanced BioScience Laboratories, Inc., Rockville, Maryland, USA.
Anthony CristilloAdvanced BioScience Laboratories, Inc., Rockville, Maryland, USA.
Giuseppe PantaleoCentre Hospitalier Universitaire Vaudois, 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, Créteil, France yves.levy@aphp.fr.
Duke Medical Center · USFred Hutch Cancer Center · USBioScience Laboratories (United States) · USArizona State University · USInserm · FRInstitut de Recherche Vaccinale · FRAssistance Publique – Hôpitaux de Paris · FRHôpital Albert-Chenevier · FROncovir (United States) · USUniversity Hospital of Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We compared the HIV-1-specific immune responses generated by targeting HIV-1 envelope protein (Env gp140) to either CD40 or LOX-1, two endocytic receptors on dendritic cells (DCs), in rhesus macaques primed with a poxvirus vector (NYVAC-KC) expressing Env gp140. The DC-targeting vaccines, humanized recombinant monoclonal antibodies fused to Env gp140, were administered as a boost with poly-ICLC adjuvant either alone or coadministered with the NYVAC-KC vector. All the DC-targeting vaccine administrations with poly-ICLC increased the low-level serum anti-Env IgG responses elicited by NYVAC-KC priming significantly more (up to a

Indexed as

AIDS VaccinesAnimalsAntibodies, NeutralizingCarboxymethylcellulose SodiumCD40 AntigensCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCHO CellsCricetulusDendritic Cellsenv Gene Products, Human Immunodeficiency VirusHIV-1HIV AntibodiesImmunoglobulin AImmunoglobulin GMacaca mulattaAIDS VaccinesAntibodies, NeutralizingCarboxymethylcellulose SodiumCD40 Antigensenv Gene Products, Human Immunodeficiency Virusgp140 envelope protein, Human immunodeficiency virus 1HIV AntibodiesImmunoglobulin AImmunoglobulin GNYVAC-C vaccineOLR1 protein, humanPoly I-Cpoly ICLCPolylysineScavenger Receptors, Class Edendritic cellsHIV-1vaccines

Identifiers

PMID28202751
PMCPMC5391468
OpenAlexW2588934593

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.