Evidence map›Paper›PMID 25504724›Full record

ArticleScience (New York, N.Y.)2014

HIV antibodies. Antigen modification regulates competition of broad and narrow neutralizing HIV antibodies.

Andrew T McGuire, Anita M Dreyer, Sara Carbonetti, Adriana Lippy, Jolene Glenn, Johannes F Scheid, Hugo Mouquet, Leonidas Stamatatos

Abstract read
In one paragraph

Article in Science (New York, N.Y.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed
8.8field-weighted citation impact, top 1% 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

100 citing papers in PubMed, 127 citations in OpenAlex.

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  13. Retrospective SARS-CoV-2 human antibody development trajectories are largely sparse and permissive.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  20. Signatures of VNature communications · 2023
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40 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Andrew T McGuire *Seattle Biomedical Research Institute, Seattle, WA 98109, USA.
Anita M Dreyer *Seattle Biomedical Research Institute, Seattle, WA 98109, USA.
Sara CarbonettiSeattle Biomedical Research Institute, Seattle, WA 98109, USA.
Adriana LippySeattle Biomedical Research Institute, Seattle, WA 98109, USA.
Jolene GlennSeattle Biomedical Research Institute, Seattle, WA 98109, USA.
Johannes F ScheidLaboratory of Molecular Immunology, The Rockefeller University, New York, NY 10065, USA.
Hugo MouquetLaboratory of Humoral Response to Pathogens, Department of Immunology, Institut Pasteur and CNRS-URA 1961, 75015 Paris, France.
Leonidas StamatatosSeattle Biomedical Research Institute, Seattle, WA 98109, USA.
Center for Infectious Disease Research · USRockefeller University · USUniversity of Washington · US

Funding

Preclinical Evaluation of Envelope Immunogens Optimized to Elicit VRCOI-class AnU19AI109632 · NIAID · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI STAMATATOS, LEONIDAS · 2014 to 2020
$25.1M
Structure/function studies of immunogen recognition by anti-HIV antibody b12P01AI094419 · NIAID · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI STAMATATOS, LEONIDAS · 2011 to 2015
$10.6M
Canadian Institutes of Health ResearchNIAID NIH HHS P01 AI094419NIAID NIH HHS P01 AI094419-01NIAID NIH HHS U19 19AI109632-01NIAID NIH HHS U19 AI109632
6 · The paper itself

Abstract

Some HIV-infected individuals develop broadly neutralizing antibodies (bNAbs), whereas most develop antibodies that neutralize only a narrow range of viruses (nNAbs). bNAbs, but not nNAbs, protect animals from experimental infection and are likely a key component of an effective vaccine. nNAbs and bNAbs target the same regions of the viral envelope glycoprotein (Env), but for reasons that remain unclear only nNAbs are elicited by Env immunization. We show that in contrast to germline-reverted (gl) bNAbs, glnNAbs recognized diverse recombinant Envs. Moreover, owing to binding affinity differences, nNAb B cell progenitors had an advantage in becoming activated and internalizing Env compared with bNAb B cell progenitors. We then identified an Env modification strategy that minimized the activation of nNAb B cells targeting epitopes that overlap those of bNAbs.

Indexed as

AIDS VaccinesAntibodies, NeutralizingAntibody AffinityBinding, CompetitiveB-Lymphocytesenv Gene Products, Human Immunodeficiency VirusEpitopesHIV-1HIV AntibodiesHumansLymphocyte ActivationModels, MolecularReceptors, Antigen, B-CellRecombinant ProteinsAIDS VaccinesAntibodies, Neutralizingenv Gene Products, Human Immunodeficiency VirusEpitopesHIV AntibodiesReceptors, Antigen, B-CellRecombinant Proteins

Identifiers

PMID25504724
PMCPMC4290850
OpenAlexW1968375364

What OpenQuestion holds

Textmetadata
LicenceTDM
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.