Evidence map›Paper›PMID 35709309›Full record

ArticlePLoS pathogens2022

Broad coverage of neutralization-resistant SIV strains by second-generation SIV-specific antibodies targeting the region involved in binding CD4.

Hugh C Welles, Hannah A D King, Leonard Nettey, Nicole Cavett, Jason Gorman, Tongqing Zhou, Yaroslav Tsybovsky, Renguang Du, Kaimei Song, Richard Nguyen and 13 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 15 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

23 authors at 6 institutions in 1 country.

Hugh C WellesVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
Hannah A D KingVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
Leonard NetteyVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
Nicole CavettVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
Jason GormanVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
Tongqing ZhouVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
Yaroslav TsybovskyVaccine Research Center Electron Microscopy Unit, Cancer Research Technology Program, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, Maryland, United States of America.
Renguang DuVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
Kaimei SongVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
Richard NguyenVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
David AmbrozakVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
Amy RansierVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
Chaim A SchrammVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
Nicole A Doria-RoseVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
Adrienne E SwanstromAIDS and Cancer Virus Program, Frederick National Laboratory for Cancer Research, Frederick, Maryland, United States of America.
James A HoxieDepartment of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Celia LaBrancheDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, United States of America.
David C MontefioriDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, United States of America.
Daniel C DouekVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
Peter D KwongVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
John R MascolaVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
Mario RoedererVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.
Rosemarie D MasonVaccine Research Center, National Institutes of Health, Bethesda, Maryland, United States of America.ORCID 0000-0001-7123-4902
National Institutes of Health · USDuke Medical Center · USFrederick National Laboratory for Cancer Research · USHenry M. Jackson Foundation · USLeidos (United States) · USUniversity of Pennsylvania · US

Funding

Neutralization Mechanisms Of Anti-HIV-1 Monoclonal AntibodiesZIAAI005022 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI ZHOU, TONGQING · 2009 to 2025
$24.6M
Isolation of Monoclonal Antiobodies Against HIVZIAAI005095 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI DORIA-ROSE, NICOLE · 2009 to 2025
$14.5M
Monoclonal antibody isolation and characterizationZIAAI005126 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MASON, ROSEMARIE · 2015 to 2025
$10.1M
Non-CD4 tropic SIV: Enhancing CD4 T-cell help in antiviral immune responsesR01AI112456 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI HOXIE, JAMES A · 2014 to 2017
$3.3M
CCR NIH HHS HHSN261200800001CNCI NIH HHS HHSN261200800001ENIAID NIH HHS HHSN272201800004CNIAID NIH HHS R01 AI112456
6 · The paper itself

Abstract

Both SIV and SHIV are powerful tools for evaluating antibody-mediated prevention and treatment of HIV-1. However, owing to a lack of rhesus-derived SIV broadly neutralizing antibodies (bnAbs), testing of bnAbs for HIV-1 prevention or treatment has thus far been performed exclusively in the SHIV NHP model using bnAbs from HIV-1-infected individuals. Here we describe the isolation and characterization of multiple rhesus-derived SIV bnAbs capable of neutralizing most isolates of SIV. Eight antibodies belonging to two clonal families, ITS102 and ITS103, which target unique epitopes in the CD4 binding site (CD4bs) region, were found to be broadly neutralizing and together neutralized all SIV strains tested. A rare feature of these bnAbs and two additional antibody families, ITS92 and ITS101, which mediate strain-specific neutralizing activity against SIV from sooty mangabeys (SIVsm), was their ability to achieve near complete (i.e. 100%) neutralization of moderately and highly neutralization-resistant SIV. Overall, these newly identified SIV bnAbs highlight the potential for evaluating HIV-1 prophylactic and therapeutic interventions using fully simian, rhesus-derived bnAbs in the SIV NHP model, thereby circumventing issues related to rapid antibody clearance of human-derived antibodies, Fc mismatch and limited genetic diversity of SHIV compared to SIV.

Indexed as

HIV-1HIV InfectionsSimian Immunodeficiency VirusAnimalsAntibodies, NeutralizingBroadly Neutralizing AntibodiesHIV AntibodiesMacaca mulattaAntibodies, NeutralizingBroadly Neutralizing AntibodiesHIV Antibodies

Identifiers

PMID35709309
PMCPMC9242510
OpenAlexW4283015296

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.