Evidence map›Paper›PMID 23103874›Full record

ArticleNature2012

HIV therapy by a combination of broadly neutralizing antibodies in humanized mice.

Florian Klein, Ariel Halper-Stromberg, Joshua A Horwitz, Henning Gruell, Johannes F Scheid, Stylianos Bournazos, Hugo Mouquet, Linda A Spatz, Ron Diskin, Alexander Abadir and 14 more

Abstract read
In one paragraph

Article in Nature, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 361 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
361citing papers in PubMed, 1 pooled it
23.5field-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

361 citing papers in PubMed, 1 synthesis or guideline pooled it, 501 citations in OpenAlex.

  1. Pooled it
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  15. Antibody feedback establishes an affinity brake in the germinal center.bioRxiv : the preprint server for biology · 2025
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301 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

24 authors at 5 institutions in 2 countries.

Florian KleinLaboratory of Molecular Immunology, The Rockefeller University; New York, New York 10065; United States.
Ariel Halper-Stromberg *Laboratory of Molecular Immunology, The Rockefeller University; New York, New York 10065; United States.
Joshua A Horwitz *Laboratory of Molecular Immunology, The Rockefeller University; New York, New York 10065; United States.
Henning GruellLaboratory of Molecular Immunology, The Rockefeller University; New York, New York 10065; United States.
Johannes F ScheidLaboratory of Molecular Immunology, The Rockefeller University; New York, New York 10065; United States.
Stylianos BournazosLaboratory of Molecular Genetics and Immunology, The Rockefeller University; New York, New York 10065; United States.
Hugo MouquetLaboratory of Molecular Immunology, The Rockefeller University; New York, New York 10065; United States.
Linda A SpatzLaboratory of Molecular Immunology, The Rockefeller University; New York, New York 10065; United States.
Ron DiskinDivision of Biology, California Institute of Technology; Pasadena, CA 91125; United States.
Alexander AbadirLaboratory of Molecular Immunology, The Rockefeller University; New York, New York 10065; United States.
Trinity ZangAaron Diamond AIDS Research Center, Laboratory of Retrovirology, The Rockefeller University; New York, New York 10065; United States.
Marcus DornerLaboratory of Virology and Infectious Diseases, The Rockefeller University; New York, New York 10065; United States.
Eva BillerbeckLaboratory of Virology and Infectious Diseases, The Rockefeller University; New York, New York 10065; United States.
Rachael N LabittLaboratory of Virology and Infectious Diseases, The Rockefeller University; New York, New York 10065; United States.
Christian GaeblerLaboratory of Molecular Immunology, The Rockefeller University; New York, New York 10065; United States.
Paola MarcovecchioDivision of Biology, California Institute of Technology; Pasadena, CA 91125; United States.
Reha-Baris IncesuLaboratory of Molecular Immunology, The Rockefeller University; New York, New York 10065; United States.
Thomas R EisenreichLaboratory of Molecular Immunology, The Rockefeller University; New York, New York 10065; United States.
Paul D BieniaszAaron Diamond AIDS Research Center, Laboratory of Retrovirology, The Rockefeller University; New York, New York 10065; United States.
Michael S SeamanBeth Israel Deaconess Med. Ctr.; Boston, MA 02215; United States.
Pamela J BjorkmanDivision of Biology, California Institute of Technology; Pasadena, CA 91125; United States.
Jeffrey V RavetchLaboratory of Molecular Genetics and Immunology, The Rockefeller University; New York, New York 10065; United States.
Alexander PlossLaboratory of Virology and Infectious Diseases, The Rockefeller University; New York, New York 10065; United States.
Michel C NussenzweigLaboratory of Molecular Immunology, The Rockefeller University; New York, New York 10065; United States.
Rockefeller University · USHoward Hughes Medical Institute · USCalifornia Institute of Technology · USBeth Israel Deaconess Medical Center · USUniversity Hospital Carl Gustav Carus · DE

Funding

Support Component D/Vaccine Discovery, Concept to ClinicUM1AI100663 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI BAROUCH, DAN H. · 2012 to 2018
$131.5M
Weill Cornell/Rockefeller/Sloan-Kettering MST ProgramT32GM007739 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI HSU, KATHARINE C · 1985 to 2023
$51.1M
Protein Expression CoreP01AI081677 · NIAID · ROCKEFELLER UNIVERSITY · PI STEINMAN, RALPH MARVIN · 2009 to 2013
$10.6M
Howard Hughes Medical InstituteNIAID NIH HHS 1UM1AI100663NIAID NIH HHS AI081677NIAID NIH HHS P01 AI081677NIGMS NIH HHS T32 GM007739
6 · The paper itself

Abstract

Human antibodies to human immunodeficiency virus-1 (HIV-1) can neutralize a broad range of viral isolates in vitro and protect non-human primates against infection. Previous work showed that antibodies exert selective pressure on the virus but escape variants emerge within a short period of time. However, these experiments were performed before the recent discovery of more potent anti-HIV-1 antibodies and their improvement by structure-based design. Here we re-examine passive antibody transfer as a therapeutic modality in HIV-1-infected humanized mice. Although HIV-1 can escape from antibody monotherapy, combinations of broadly neutralizing antibodies can effectively control HIV-1 infection and suppress viral load to levels below detection. Moreover, in contrast to antiretroviral therapy, the longer half-life of antibodies led to control of viraemia for an average of 60 days after cessation of therapy. Thus, combinations of potent monoclonal antibodies can effectively control HIV-1 replication in humanized mice, and should be re-examined as a therapeutic modality in HIV-1-infected individuals.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, NeutralizingAntibody SpecificityDisease Models, AnimalHalf-LifeHIV-1HIV AntibodiesHIV InfectionsHumansImmunization, PassiveMiceMice, Inbred NODTime FactorsViral LoadAntibodies, MonoclonalAntibodies, NeutralizingHIV Antibodies

Identifiers

PMID23103874
PMCPMC3809838
OpenAlexW2081313987

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.