Evidence map›Paper›PMID 29437967›Full record

ArticleJournal of virology2018

Immunogenicity of NYVAC Prime-Protein Boost Human Immunodeficiency Virus Type 1 Envelope Vaccination and Simian-Human Immunodeficiency Virus Challenge of Nonhuman Primates.

Kevin O Saunders, Sampa Santra, Robert Parks, Nicole L Yates, Laura L Sutherland, Richard M Scearce, Harikrishnan Balachandran, Todd Bradley, Derrick Goodman, Amanda Eaton and 16 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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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

26 authors at 8 institutions in 3 countries.

Kevin O SaundersDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA kevin.saunders@dm.duke.edu barton.haynes@duke.edu.
Sampa SantraBeth Israel Deaconess Medical Center, Harvard University School of Medicine, Boston, Massachusetts, USA.
Robert ParksDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Nicole L YatesDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Laura L SutherlandDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Richard M ScearceDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Harikrishnan BalachandranBeth Israel Deaconess Medical Center, Harvard University School of Medicine, Boston, Massachusetts, USA.
Todd BradleyDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Derrick GoodmanDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Amanda EatonDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Sherry A Stanfield-OakleyDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, USA.
James TartagliaDepartment of Research and Development, Sanofi Pasteur, Swiftwater, Pennsylvania, USA.
Sanjay PhogatDepartment of Research and Development, Sanofi Pasteur, Swiftwater, Pennsylvania, USA.
Giuseppe PantaleoDivision of Immunology, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.
Mariano EstebanDepartment of Molecular and Cellular Biology, Centro Nacional de Biotecnologia, CSIC, Madrid, Spain.
Carmen E GomezDepartment of Molecular and Cellular Biology, Centro Nacional de Biotecnologia, CSIC, Madrid, Spain.
Beatriz PerdigueroDepartment of Molecular and Cellular Biology, Centro Nacional de Biotecnologia, CSIC, Madrid, Spain.
Bertram JacobsBiodesign Institute, School of Life Sciences, Arizona State University, Tempe, Arizona, USA.
Karen KiblerBiodesign Institute, School of Life Sciences, Arizona State University, Tempe, Arizona, USA.
Bette KorberLos Alamos National Laboratory and New Mexico Consortium, Los Alamos, New Mexico, USA.
David C MontefioriDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, USA.
Guido FerrariDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, USA.
Nathan VandergriftDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Hua-Xin LiaoDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Georgia D TomarasDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0001-8076-1931
Barton F HaynesDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA kevin.saunders@dm.duke.edu barton.haynes@duke.edu.
Duke Medical Center · USCentro Nacional de Biotecnología · ESArizona State University · USBeth Israel Deaconess Medical Center · USSanofi (United States) · USDuke University · USLos Alamos National Laboratory · USSwiss Vaccine Research Institute · CH

Funding

Virus biology scientific research support componentUM1AI100645 · NIAID · DUKE UNIVERSITY · PI HAHN, BEATRICE H · 2012 to 2018
$204.7M
Social and Behavioral Sciences CoreP30AI064518 · NIAID · DUKE UNIVERSITY · PI GEORGIA Doris TOMARAS · 2005 to 2026
$50.5M
Virus and Antibody Gene Sequencing CoreP01AI131251 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI Kevin Wiehe · 2017 to 2026
$40.7M
Viral and Host Determinants of HIV-1 TransmissionU01AI067854 · NIAID · DUKE UNIVERSITY · PI HAYNES, BARTON F · 2005 to 2005
$14.9M
HIV-1 vaccine-elicited antibodies target envelope glycansR01AI120801 · NIAID · DUKE UNIVERSITY · PI SAUNDERS, KEVIN O · 2015 to 2024
$7.5M
NIAID NIH HHS P01 AI131251NIAID NIH HHS P30 AI064518NIAID NIH HHS R01 AI120801NIAID NIH HHS U01 AI067854NIAID NIH HHS UM1 AI100645
6 · The paper itself

Abstract

A preventive human immunodeficiency virus type 1 (HIV-1) vaccine is an essential part of the strategy to eradicate AIDS. A critical question is whether antibodies that do not neutralize primary isolate (tier 2) HIV-1 strains can protect from infection. In this study, we investigated the ability of an attenuated poxvirus vector (NYVAC) prime-envelope gp120 boost to elicit potentially protective antibody responses in a rhesus macaque model of mucosal simian-human immunodeficiency virus (SHIV) infection. NYVAC vector delivery of a group M consensus envelope, trivalent mosaic envelopes, or a natural clade B isolate B.1059 envelope elicited antibodies that mediated neutralization of tier 1 viruses, cellular cytotoxicity, and phagocytosis. None of the macaques made neutralizing antibodies against the tier 2 SHIV SF162P3 used for mucosal challenge. Significant protection from infection was not observed for the three groups of vaccinated macaques compared to unvaccinated macaques, although binding antibody to HIV-1 Env correlated with decreased viremia after challenge. Thus, NYVAC Env prime-gp120 boost vaccination elicited polyfunctional, nonneutralizing antibody responses with minimal protective activity against tier 2 SHIV mucosal challenge.

Indexed as

Immunization, SecondaryImmunogenicity, VaccineAIDS VaccinesAnimalsenv Gene Products, Human Immunodeficiency VirusHIV-1HumansMacaca mulattaSimian Immunodeficiency VirusAIDS Vaccinesenv Gene Products, Human Immunodeficiency VirusHIVHIV vaccineneutralizing antibodiessimian-human immunodeficiency virus

Identifiers

PMID29437967
PMCPMC5874432
OpenAlexW2786796514

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.