Evidence map›Paper›PMID 26925256›Full record

ArticleSignal transduction and targeted therapy

Intravenous immune globulin suppresses angiogenesis in mice and humans.

Reo Yasuma, Valeria Cicatiello, Takeshi Mizutani, Laura Tudisco, Younghee Kim, Valeria Tarallo, Sasha Bogdanovich, Yoshio Hirano, Nagaraj Kerur, Shengjian Li and 16 more

Open access · goldAbstract read
In one paragraph

Article in Signal transduction and targeted therapy. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.4field-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

17 citing papers in PubMed, 27 citations in OpenAlex.

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  13. New Therapies of Neovascular AMD-Beyond Anti-VEGFs.Vision (Basel, Switzerland) · 2018
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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

26 authors at 9 institutions in 6 countries.

Reo YasumaDepartment of Ophthalmology and Visual Sciences, University of Kentucky, Lexington, KY, USA; Department of Ophthalmology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Valeria CicatielloAngiogenesis Lab, Institute of Genetics and Biophysics-CNR, Naples, Italy; Bio-Ker, MultiMedica Group, Naples, Italy.
Takeshi MizutaniDepartment of Ophthalmology and Visual Sciences, University of Kentucky, Lexington, KY, USA.
Laura TudiscoAngiogenesis Lab, Institute of Genetics and Biophysics-CNR, Naples, Italy.
Younghee KimDepartment of Ophthalmology and Visual Sciences, University of Kentucky, Lexington, KY, USA.
Valeria TaralloDepartment of Ophthalmology and Visual Sciences, University of Kentucky, Lexington, KY, USA; Angiogenesis Lab, Institute of Genetics and Biophysics-CNR, Naples, Italy.
Sasha BogdanovichDepartment of Ophthalmology and Visual Sciences, University of Kentucky, Lexington, KY, USA.
Yoshio HiranoDepartment of Ophthalmology and Visual Sciences, University of Kentucky, Lexington, KY, USA.
Nagaraj KerurDepartment of Ophthalmology and Visual Sciences, University of Kentucky, Lexington, KY, USA.
Shengjian LiDepartment of Ophthalmology and Visual Sciences, University of Kentucky, Lexington, KY, USA.
Tetsuhiro YasumaDepartment of Ophthalmology and Visual Sciences, University of Kentucky, Lexington, KY, USA.
Benjamin J FowlerDepartment of Ophthalmology and Visual Sciences, University of Kentucky, Lexington, KY, USA; Department of Physiology, University of Kentucky, Lexington, KY, USA.
Charles B WrightDepartment of Ophthalmology and Visual Sciences, University of Kentucky, Lexington, KY, USA.
Ivana ApicellaAngiogenesis Lab, Institute of Genetics and Biophysics-CNR, Naples, Italy.
Adelaide GrecoDepartment of Advanced Biomedical Sciences, University of Naples 'Federico II', Naples, Italy; CEINGE-Biotecnologie Avanzate, s.c. ar.l., Naples, Italy.
Arturo BrunettiDepartment of Advanced Biomedical Sciences, University of Naples 'Federico II', Naples, Italy; CEINGE-Biotecnologie Avanzate, s.c. ar.l., Naples, Italy.
Balamurali K AmbatiDepartment of Ophthalmology and Visual Sciences, Moran Eye Center, University of Utah School of Medicine, Salt Lake City, UT, USA; Department of Ophthalmology, Veterans Affairs Salt Lake City Healthcare System, Salt Lake City, UT, USA.
Sevim Barbasso HelmersRheumatology Unit, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Ingrid E LundbergRheumatology Unit, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Ondrej ViklickyDepartment of Nephrology, Institute for Clinical and Experimental Medicine, Prague 4, Czech Republic.
Jeanette Hw LeusenImmunotherapy Laboratory, Laboratory for Translational Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
J Sjef VerbeekDepartment of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Bradley D GelfandDepartment of Ophthalmology and Visual Sciences, University of Kentucky, Lexington, KY, USA; Department of Biomedical Engineering, University of Kentucky, Lexington, KY, USA; Department of Microbiology, Immunology, and Molecular Genetics, University of Kentucky, Lexington, KY, USA.
Ana Bastos-CarvalhoDepartment of Ophthalmology and Visual Sciences, University of Kentucky, Lexington, KY, USA.
Sandro De FalcoAngiogenesis Lab, Institute of Genetics and Biophysics-CNR, Naples, Italy; IRCCS MultiMedica, Milano, Italy.
Jayakrishna AmbatiDepartment of Ophthalmology and Visual Sciences, University of Kentucky, Lexington, KY, USA; Department of Physiology, University of Kentucky, Lexington, KY, USA.
University of Kentucky · USInstitute of Genetics and Biophysics · ITCeinge Biotecnologie Avanzate (Italy) · ITKarolinska University Hospital · SEInstitute of Clinical and Experimental Medicine · CZLeiden University Medical Center · NLMultiMedica · ITUniversity Medical Center Utrecht · NLUniversity of Utah · US

Funding

The Role of Soluble Flt-1 and Raver2 in Ocular Vascular DemarcationsR01EY017950 · NEI · UNIVERSITY OF UTAH · PI AMBATI, BALAMURALI K · 2008 to 2021
$5.2M
Form and function of our Janus faced genomeDP1GM114862 · NIGMS · UNIVERSITY OF VIRGINIA · PI AMBATI, JAYAKRISHNA · 2014 to 2018
$4.0M
Intraceptor Interference of VEGF PathwaysR01EY017182 · NEI · UNIVERSITY OF UTAH · PI AMBATI, BALAMURALI K · 2007 to 2017
$3.6M
KENTUCKY CENTER FOR CLINICAL AND TRANSLATIONAL SCIENCEUL1RR033173 · NCRR · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2011 to 2011
$3.5M
Functional studies of DICER1 and Alu RNA in geographic atrophyR01EY022238 · NEI · UNIVERSITY OF VIRGINIA · PI AMBATI, JAYAKRISHNA · 2012 to 2016
$3.3M
Inflammasome Activation in Geographic AtrophyR01EY024068 · NEI · UNIVERSITY OF VIRGINIA · PI AMBATI, JAYAKRISHNA · 2014 to 2017
$2.6M
Clinical Scholars In Cardiovascular ScienceT32HL091812 · NHLBI · UNIVERSITY OF KENTUCKY · PI SMYTH, SUSAN S. · 2008 to 2018
$2.3M
Pro-and anti-angiogenic effects of vascular endothelial growth factor-AR01EY018350 · NEI · UNIVERSITY OF KENTUCKY · PI AMBATI, JAYAKRISHNA · 2007 to 2011
$1.9M
Intrinsic anti-angiogenic activity of siRNAR01EY018836 · NEI · UNIVERSITY OF KENTUCKY · PI AMBATI, JAYAKRISHNA · 2008 to 2011
$1.9M
Endogenous Specific Inhibitor of Corneal LymphangiogenesisR01EY020672 · NEI · UNIVERSITY OF KENTUCKY · PI AMBATI, JAYAKRISHNA · 2010 to 2013
$1.5M
Non-canonical NLRP3 Inflammasome Activation in Geographic AtrophyR00EY024336 · NEI · UNIVERSITY OF VIRGINIA · PI KERUR, NAGARAJ · 2016 to 2018
$747k
Non-canonical NLRP3 Inflammasome Activation in Geographic AtrophyK99EY024336 · NEI · UNIVERSITY OF KENTUCKY · PI KERUR, NAGARAJ · 2014 to 2015
$175k
NCRR NIH HHS UL1 RR033173NEI NIH HHS K99 EY024336NEI NIH HHS R00 EY024336NEI NIH HHS R01 EY017182NEI NIH HHS R01 EY017950NEI NIH HHS R01 EY018350NEI NIH HHS R01 EY018836NEI NIH HHS R01 EY020672NEI NIH HHS R01 EY022238NEI NIH HHS R01 EY024068NHLBI NIH HHS T32 HL091812NIGMS NIH HHS DP1 GM114862
6 · The paper itself

Abstract

Human intravenous immune globulin (IVIg), a purified IgG fraction composed of ~ 60% IgG1 and obtained from the pooled plasma of thousands of donors, is clinically used for a wide range of diseases. The biological actions of IVIg are incompletely understood and have been attributed both to the polyclonal antibodies therein and also to their IgG (IgG) Fc regions. Recently, we demonstrated that multiple therapeutic human IgG1 antibodies suppress angiogenesis in a target-independent manner via FcγRI, a high-affinity receptor for IgG1. Here we show that IVIg possesses similar anti-angiogenic activity and inhibited blood vessel growth in five different mouse models of prevalent human diseases, namely, neovascular age-related macular degeneration, corneal neovascularization, colorectal cancer, fibrosarcoma and peripheral arterial ischemic disease. Angioinhibition was mediated by the Fc region of IVIg, required FcγRI and had similar potency in transgenic mice expressing human FcγRs. Finally, IVIg therapy administered to humans for the treatment of inflammatory or autoimmune diseases reduced kidney and muscle blood vessel densities. These data place IVIg, an agent approved by the US Food and Drug Administration, as a novel angioinhibitory drug in doses that are currently administered in the clinical setting. In addition, they raise the possibility of an unintended effect of IVIg on blood vessels.

Identifiers

PMID26925256
PMCPMC4768485
OpenAlexW2266260677

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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.