Evidence map›Paper›PMID 29281818›Full record

ArticleCell reports2017

Vaccine Induction of Heterologous Tier 2 HIV-1 Neutralizing Antibodies in Animal Models.

Kevin O Saunders, Laurent K Verkoczy, Chuancang Jiang, Jinsong Zhang, Robert Parks, Haiyan Chen, Max Housman, Hilary Bouton-Verville, Xiaoying Shen, Ashley M Trama and 24 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
8.1field-weighted citation impact, top 2% 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

82 citing papers in PubMed, 103 citations in OpenAlex.

  1. Trial
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  3. Priming of Multiple HIV Neutralizing B Cell Precursors in Humans.medRxiv : the preprint server for health sciences · 2026
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22 more citing papers are in PubMed but not listed here.

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

34 authors at 10 institutions in 2 countries.

Kevin O SaundersDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA; Department of Surgery, Duke School of Medicine, Durham, NC 27710, USA. Electronic address: kevin.saunders@duke.edu.
Laurent K VerkoczyDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA; Department of Pathology, Duke School of Medicine, Durham, NC 27710, USA. Electronic address: laurent.verkoczy@duke.edu.
Chuancang JiangDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA.
Jinsong ZhangDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA.
Robert ParksDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA.
Haiyan ChenDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA.
Max HousmanDepartment of Cell Biology, Duke University, Duke University Medical Center, Durham, NC 27710, USA.
Hilary Bouton-VervilleDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA.
Xiaoying ShenDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA.
Ashley M TramaDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA.
Richard ScearceDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA.
Laura SutherlandDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA.
Sampa SantraBeth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Amanda NewmanDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA.
Amanda EatonDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA; Department of Surgery, Duke School of Medicine, Durham, NC 27710, USA.
Kai XuVaccine Research Center, National Institute of Allergy and Infectious Disease, Bethesda, MD 20814, USA.
Ivelin S GeorgievVaccine Research Center, National Institute of Allergy and Infectious Disease, Bethesda, MD 20814, USA.
M Gordon JoyceVaccine Research Center, National Institute of Allergy and Infectious Disease, Bethesda, MD 20814, USA.
Georgia D TomarasDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA; Department of Surgery, Duke School of Medicine, Durham, NC 27710, USA.
Mattia BonsignoriDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA.
Steven G ReedInfectious Disease Research Institute, Seattle, WA 98102, USA.
Andres SalazarOncovir, Inc., Washington, DC 20008, USA.
John R MascolaVaccine Research Center, National Institute of Allergy and Infectious Disease, Bethesda, MD 20814, USA.
M Anthony MoodyDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA; Department of Pediatrics, Duke School of Medicine, Durham, NC 27710, USA.
Derek W CainDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA.
Mireille CentlivreVaccine Research Institute (VRI), Inserm U955, Université Paris Est, AP-HP, Hôpital H. Mondor - A. Chenevier, Créteil, 94000, France.
Sandra ZurawskiBaylor Institute for Immunology Research, Dallas, TX 75204, USA; Vaccine Research Institute (VRI), Inserm U955, Université Paris Est, AP-HP, Hôpital H. Mondor - A. Chenevier, Créteil, 94000, France.
Gerard ZurawskiBaylor Institute for Immunology Research, Dallas, TX 75204, USA; Vaccine Research Institute (VRI), Inserm U955, Université Paris Est, AP-HP, Hôpital H. Mondor - A. Chenevier, Créteil, 94000, France.
Harold P EricksonDepartment of Cell Biology, Duke University, Duke University Medical Center, Durham, NC 27710, USA.
Peter D KwongVaccine Research Center, National Institute of Allergy and Infectious Disease, Bethesda, MD 20814, USA.
S Munir AlamDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA; Department of Biomedical Engineering, Duke Pratt School of Engineering, Durham, NC 27710, USA.
Yves LevyVaccine Research Institute (VRI), Inserm U955, Université Paris Est, AP-HP, Hôpital H. Mondor - A. Chenevier, Créteil, 94000, France.
David C MontefioriDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA; Department of Surgery, Duke School of Medicine, Durham, NC 27710, USA.
Barton F HaynesDuke Human Vaccine Institute, Duke School of Medicine, Durham, NC 27710, USA; Department of Medicine and Immunology, Duke School of Medicine, Durham, NC 27710, USA. Electronic address: barton.haynes@dm.duke.edu.
Duke University · USNational Institute of Allergy and Infectious Diseases · USAssistance Publique – Hôpitaux de Paris · FRBaylor University · USBeth Israel Deaconess Medical Center · USDuke University Hospital · USHôpital Albert-Chenevier · FRInfectious Disease Research Institute · USOncovir (United States) · USPratt Institute · US

Funding

Virus biology scientific research support componentUM1AI100645 · NIAID · DUKE UNIVERSITY · PI MCMICHAEL, ANDREW JAMES · 2012 to 2018
$204.7M
Virus and Antibody Gene Sequencing CoreP01AI131251 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI Kevin Wiehe · 2017 to 2026
$40.7M
Design Of ImmunogensZIAAI005024 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI ZHOU, TONGQING · 2009 to 2025
$21.5M
HIV-1 vaccine-elicited antibodies target envelope glycansR01AI120801 · NIAID · DUKE UNIVERSITY · PI SAUNDERS, KEVIN O · 2015 to 2024
$7.5M
MPER broadly neutralizing antibody knockin mice to study anti-HIV Bcell responsesR01AI087202 · NIAID · SAN DIEGO BIOMEDICAL RESEARCH INSTITUTE · PI VERKOCZY, LAURENT KARL · 2010 to 2022
$5.5M
Dissection of polyreactivity and neutralization activity of HIV-1 AbsR01AI118571 · NIAID · DUKE UNIVERSITY · PI PERFECT, JOHN R., VERKOCZY, LAURENT KARL · 2016 to 2020
$3.2M
NIAID NIH HHS P01 AI131251NIAID NIH HHS R01 AI087202NIAID NIH HHS R01 AI118571NIAID NIH HHS R01 AI120801NIAID NIH HHS UM1 AI100645
6 · The paper itself

Abstract

The events required for the induction of broad neutralizing antibodies (bnAbs) following HIV-1 envelope (Env) vaccination are unknown, and their induction in animal models as proof of concept would be critical. Here, we describe the induction of plasma antibodies capable of neutralizing heterologous primary (tier 2) HIV-1 strains in one macaque and two rabbits. Env immunogens were designed to induce CD4 binding site (CD4bs) bnAbs, but surprisingly, the macaque developed V1V2-glycan bnAbs. Env immunization of CD4bs bnAb heavy chain rearrangement (V

Indexed as

AIDS VaccinesAmino Acid SequenceAnimalsAntibodies, NeutralizingDisease Models, Animalenv Gene Products, Human Immunodeficiency VirusEpitopesHIV-1HIV AntibodiesImmunizationMacaca mulattaMicePolysaccharidesProtein MultimerizationRabbitsAIDS VaccinesAntibodies, Neutralizingenv Gene Products, Human Immunodeficiency VirusEpitopesHIV AntibodiesPolysaccharidesbroadly neutralizing antibodiesCH103CH505HIV vaccineknockin mice

Identifiers

PMID29281818
PMCPMC5777169
OpenAlexW2777283909

What OpenQuestion holds

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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.