Evidence map›Paper›PMID 24172896›Full record

ArticleNature2013

Antibody-mediated immunotherapy of macaques chronically infected with SHIV suppresses viraemia.

Masashi Shingai, Yoshiaki Nishimura, Florian Klein, Hugo Mouquet, Olivia K Donau, Ronald Plishka, Alicia Buckler-White, Michael Seaman, Michael Piatak, Jeffrey D Lifson and 3 more

2 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in Nature, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 310 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
310citing papers in PubMed, 1 pooled it
24.1field-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.

NCT02471326 phase1completednot on this mapstarted 2015, after this paper: background citation

An Exploratory, Open-Label Study of VRC-HIVMAB060-00-AB (VRC01) in Subjects With Chronic HIV Infection Undergoing Analytical Treatment Interruption

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2015 to 2017Enrolled10ConditionsHIVArmsVRC-HIVMAB060-00-AB (VRC01)
NCT03468582 early_phase1completednot on this mapstarted 2018, after this paper: background citation

Pilot Study Using 123I Radiolabeled 3BNC117 SPECT/CT to Image HIV Reservoir in Chronically Infected HIV Patients

TypeinterventionalSponsorUniversity of Lausanne HospitalsRan2018 to 2020Enrolled6ConditionsHuman Immunodeficiency VirusArms123I radiolabeled 3BNC117
3 · Its place in the literature

Who cites it

310 citing papers in PubMed, 1 synthesis or guideline pooled it, 452 citations in OpenAlex.

  1. Pooled it
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  18. Searching for a HIV-1 Cure.Theranostics · 2026
    Review
  19. Article
  20. Article

250 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 7 institutions in 2 countries.

Masashi Shingai1] Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA [2].
Yoshiaki Nishimura
Florian Klein
Hugo Mouquet
Olivia K Donau
Ronald Plishka
Alicia Buckler-White
Michael Seaman
Michael Piatak
Jeffrey D Lifson
Dimiter S Dimitrov
Michel C Nussenzweig
Malcolm A Martin
National Institute of Allergy and Infectious Diseases · USFrederick National Laboratory for Cancer Research · USNational Institutes of Health · USBeth Israel Deaconess Medical Center · USHoward Hughes Medical Institute · USInstitut Pasteur · FRRockefeller University · US

Funding

Stuctural basis of bNab activityP01AI100148 · NIAID · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI Pamela J Bjorkman · 2013 to 2026
$43.3M
Primate Lentivirus PathogenesisZIAAI000998 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MARTIN, MALCOLM · 2009 to 2015
$11.3M
Molecular Biology Of Retroviruses Associated With AIDSZIAAI000415 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MARTIN, MALCOLM · 2009 to 2015
$11.3M
Antibody-based therapeutics and vaccines against AIDSZIABC011155 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DIMITROV, DIMITER S · 2009 to 2017
$2.6M
CCR NIH HHS HHSN261200800001CHoward Hughes Medical InstituteIntramural NIH HHS ZIA AI000415NCI NIH HHS HHSN261200800001ENIAID NIH HHS P01 AI100148
6 · The paper itself

Abstract

Neutralizing antibodies can confer immunity to primate lentiviruses by blocking infection in macaque models of AIDS. However, earlier studies of anti-human immunodeficiency virus type 1 (HIV-1) neutralizing antibodies administered to infected individuals or humanized mice reported poor control of virus replication and the rapid emergence of resistant variants. A new generation of anti-HIV-1 monoclonal antibodies, possessing extraordinary potency and breadth of neutralizing activity, has recently been isolated from infected individuals. These neutralizing antibodies target different regions of the HIV-1 envelope glycoprotein including the CD4-binding site, glycans located in the V1/V2, V3 and V4 regions, and the membrane proximal external region of gp41 (refs 9-14). Here we have examined two of the new antibodies, directed to the CD4-binding site and the V3 region (3BNC117 and 10-1074, respectively), for their ability to block infection and suppress viraemia in macaques infected with the R5 tropic simian-human immunodeficiency virus (SHIV)-AD8, which emulates many of the pathogenic and immunogenic properties of HIV-1 during infections of rhesus macaques. Either antibody alone can potently block virus acquisition. When administered individually to recently infected macaques, the 10-1074 antibody caused a rapid decline in virus load to undetectable levels for 4-7 days, followed by virus rebound during which neutralization-resistant variants became detectable. When administered together, a single treatment rapidly suppressed plasma viraemia for 3-5 weeks in some long-term chronically SHIV-infected animals with low CD4(+) T-cell levels. A second cycle of anti-HIV-1 monoclonal antibody therapy, administered to two previously treated animals, successfully controlled virus rebound. These results indicate that immunotherapy or a combination of immunotherapy plus conventional antiretroviral drugs might be useful as a treatment for chronically HIV-1-infected individuals experiencing immune dysfunction.

Indexed as

ImmunotherapyAnimalsAntibodies, NeutralizingBinding SitesCD4 AntigensHIV-1HIV AntibodiesHIV Envelope Protein gp120MacacaMolecular Sequence DataPeptide FragmentsSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusTime FactorsViral LoadViremiaAntibodies, NeutralizingCD4 AntigensHIV AntibodiesHIV Envelope Protein gp120HIV envelope protein gp120 (305-321)Peptide Fragments

Identifiers

PMID24172896
PMCPMC4133787
OpenAlexW1989174077

What OpenQuestion holds

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Registered trials

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.