Evidence map›Paper›PMID 20368576›Full record

ArticleThe Journal of experimental medicine2010

Anti-phospholipid human monoclonal antibodies inhibit CCR5-tropic HIV-1 and induce beta-chemokines.

M Anthony Moody, Hua-Xin Liao, S Munir Alam, Richard M Scearce, M Kelly Plonk, Daniel M Kozink, Mark S Drinker, Ruijun Zhang, Shi-Mao Xia, Laura L Sutherland and 18 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

35 citing papers in PubMed, 55 citations in OpenAlex.

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  12. Efferocytosis of Pathogen-Infected Cells.Frontiers in immunology · 2017
    Review
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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

28 authors at 9 institutions in 3 countries.

M Anthony MoodyDuke Human Vaccine Institute, Duke University Medical Center, Durham, NC 27710, USA. moody007@mc.duke.edu
Hua-Xin Liao
S Munir Alam
Richard M Scearce
M Kelly Plonk
Daniel M Kozink
Mark S Drinker
Ruijun Zhang
Shi-Mao Xia
Laura L Sutherland
Georgia D Tomaras
Ian P Giles
John C Kappes
Christina Ochsenbauer-Jambor
Tara G Edmonds
Melina Soares
Gustavo Barbero
Donald N Forthal
Gary Landucci
Connie Chang
Steven W King
Anita Kavlie
Thomas N Denny
Kwan-Ki Hwang
Pojen P Chen
Philip E Thorpe
David C Montefiori
Barton F Haynes
International Vaccine Institute · KRPediatrics and Genetics · USThe University of Texas Southwestern Medical Center · USUniversity of Alabama at Birmingham · USAvid Bioservices (United States) · USUniversity of California, Irvine · USDuke Medical Center · USUniversity College London · GBUniversity of California, Los Angeles · US

Funding

Viral Sequencing CoreU19AI067854 · NIAID · DUKE UNIVERSITY · PI HARRISON, STEPHEN COPLAN · 2006 to 2011
$290.5M
Virology CoreP30AI027767 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI OLAF KUTSCH · 1988 to 2026
$84.1M
Regional Biocontainment Laboratory (RBL)UC6AI058607 · NIAID · DUKE UNIVERSITY · PI WILLIAMS, R SANDERS · 2003 to 2005
$16.3M
Duke University Center for Translational ResearchP30AI051445 · NIAID · DUKE UNIVERSITY · PI FROTHINGHAM, RICHARD · 2002 to 2006
$8.1M
Mucosal HIV and Immunobiology CenterR24DK064400 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SMITH, PHILLIP D · 2003 to 2012
$4.8M
NIAID NIH HHS P30 AI027767NIAID NIH HHS P30 AI051445NIAID NIH HHS P30-AI-27767NIAID NIH HHS P30 AI51445NIAID NIH HHS U19 AI067854NIAID NIH HHS UC6 AI058607NIAID NIH HHS UC6 AI58607NIDDK NIH HHS R24 DK064400NIDDK NIH HHS R24DK64400
6 · The paper itself

Abstract

Traditional antibody-mediated neutralization of HIV-1 infection is thought to result from the binding of antibodies to virions, thus preventing virus entry. However, antibodies that broadly neutralize HIV-1 are rare and are not induced by current vaccines. We report that four human anti-phospholipid monoclonal antibodies (mAbs) (PGN632, P1, IS4, and CL1) inhibit HIV-1 CCR5-tropic (R5) primary isolate infection of peripheral blood mononuclear cells (PBMCs) with 80% inhibitory concentrations of <0.02 to approximately 10 microg/ml. Anti-phospholipid mAbs inhibited PBMC HIV-1 infection in vitro by mechanisms involving binding to monocytes and triggering the release of MIP-1alpha and MIP-1beta. The release of these beta-chemokines explains both the specificity for R5 HIV-1 and the activity of these mAbs in PBMC cultures containing both primary lymphocytes and monocytes.

Indexed as

Antibodies, AntiphospholipidAntibodies, Monoclonalbeta 2-Glycoprotein ICardiolipinsCD4-Positive T-LymphocytesCell FusionChemokine CCL3Chemokine CCL4ChemokinesChemokines, CCComplementarity Determining RegionsCulture Media, ConditionedEndotoxinsenv Gene Products, Human Immunodeficiency VirusEpithelial CellsGiant Cells1,2-dioleoyl-glycero-3-phosphatidyl ethanolamineAntibodies, AntiphospholipidAntibodies, Monoclonalbeta 2-Glycoprotein ICardiolipinsCCL3 protein, humanCCL4 protein, humanChemokine CCL3Chemokine CCL4ChemokinesChemokines, CCComplementarity Determining RegionsCulture Media, ConditionedEndotoxinsenv Gene Products, Human Immunodeficiency VirusImmunoglobulin Fab FragmentsImmunoglobulin Fc FragmentsPhosphatidylethanolaminesPhosphatidylserinesReceptors, CCR5

Identifiers

PMID20368576
PMCPMC2856026
OpenAlexW2159824428

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.