Evidence map›Paper›PMID 35003053›Full record

ArticleFrontiers in immunology2021

Polyclonal Broadly Neutralizing Antibody Activity Characterized by CD4 Binding Site and V3-Glycan Antibodies in a Subset of HIV-1 Virus Controllers.

Tinashe E Nyanhete, Robert J Edwards, Celia C LaBranche, Katayoun Mansouri, Amanda Eaton, S Moses Dennison, Kevin O Saunders, Derrick Goodman, Katarzyna Janowska, Rachel L Spreng and 9 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. 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
0.4field-weighted citation impact, top 41% 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, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Incompletely closed HIV-1Npj viruses · 2025
    Article
  4. HIV controllers: hope for a functional cure.Frontiers in immunology · 2025
    Review
  5. Article
  6. Article
  7. Article
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

19 authors at 3 institutions in 1 country.

Tinashe E NyanheteCenter for Human Systems Immunology, Duke University School of Medicine, Durham, NC, United States.
Robert J EdwardsDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Celia C LaBrancheDepartment of Surgery, Duke University School of Medicine, Durham, NC, United States.
Katayoun MansouriDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Amanda EatonDepartment of Surgery, Duke University School of Medicine, Durham, NC, United States.
S Moses DennisonCenter for Human Systems Immunology, Duke University School of Medicine, Durham, NC, United States.
Kevin O SaundersDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Derrick GoodmanCenter for Human Systems Immunology, Duke University School of Medicine, Durham, NC, United States.
Katarzyna JanowskaDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Rachel L SprengCenter for Human Systems Immunology, Duke University School of Medicine, Durham, NC, United States.
Lu ZhangCenter for Human Systems Immunology, Duke University School of Medicine, Durham, NC, United States.
Sarah V MudrakCenter for Human Systems Immunology, Duke University School of Medicine, Durham, NC, United States.
Thomas J HopeDepartment of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.
Bhavna HoraDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Todd BradleyDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Ivelin S GeorgievVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, United States.
David C MontefioriDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Priyamvada AcharyaDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Georgia D TomarasCenter for Human Systems Immunology, Duke University School of Medicine, Durham, NC, United States.
Duke University · USNorthwestern University · USVanderbilt University Medical Center · US

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
Physical Resources CoreP01AI120756 · NIAID · DUKE UNIVERSITY · PI TOMARAS, GEORGIA DORIS · 2016 to 2020
$17.1M
Targeting early metastable intermediates of the SARS-CoV-2 spike for vaccine and therapeutics developmentR01AI145687 · NIAID · DUKE UNIVERSITY · PI Priyamvada Acharya · 2019 to 2026
$6.9M
Neutralization Fingerprinting Analysis of Polyclonal Antibody Responses against HIV-1R01AI131722 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GEORGIEV, IVELIN · 2017 to 2021
$4.5M
HIV-1 Gene Suppression by CD8+ T CellsR56AI052779 · NIAID · DUKE UNIVERSITY · PI TOMARAS, GEORGIA DORIS · 2012 to 2012
$388k
NIAID NIH HHS P01 AI120756NIAID NIH HHS P30 AI064518NIAID NIH HHS R01 AI131722NIAID NIH HHS R01 AI145687NIAID NIH HHS R56 AI052779NIAID NIH HHS UM1 AI100645
6 · The paper itself

Abstract

Broadly neutralizing antibodies (bNAbs), known to mediate immune control of HIV-1 infection, only develop in a small subset of HIV-1 infected individuals. Despite being traditionally associated with patients with high viral loads, bNAbs have also been observed in therapy naïve HIV-1+ patients naturally controlling virus replication [Virus Controllers (VCs)]. Thus, dissecting the bNAb response in VCs will provide key information about what constitutes an effective humoral response to natural HIV-1 infection. In this study, we identified a polyclonal bNAb response to natural HIV-1 infection targeting CD4 binding site (CD4bs), V3-glycan, gp120-gp41 interface and membrane-proximal external region (MPER) epitopes on the HIV-1 envelope (Env). The polyclonal antiviral antibody (Ab) response also included antibody-dependent cellular phagocytosis of clade AE, B and C viruses, consistent with both the Fv and Fc domain contributing to function. Sequence analysis of

Indexed as

SurvivorsAntibody SpecificityBinding Sites, AntibodyBroadly Neutralizing AntibodiesCD4 AntigensCD4 Lymphocyte CountEpitope MappingEpitopesFemaleGenes, envHIV-1HIV AntibodiesHIV Envelope Protein gp120HIV InfectionsHLA-B AntigensHumansBroadly Neutralizing AntibodiesCD4 AntigensEpitopesHIV AntibodiesHIV Envelope Protein gp120HIV envelope protein gp120 (305-321)HLA-B57 antigenHLA-B AntigensImmunoglobulin Fc FragmentsImmunoglobulin Fragmentsimmunoglobulin FvPeptide FragmentsRecombinant Proteinsantibody-dependent cellular phagocytosis (ADCP)broadly neutralizing antibodiesCD4-binding site antibodiesHIV-1 Virus Controllersnegative-stain electron microscopyneutralization fingerprinting assay

Identifiers

PMID35003053
PMCPMC8733328
OpenAlexW4200342842

What OpenQuestion holds

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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.