Evidence map›Paper›PMID 28130494›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

Oxidized Low-Density Lipoprotein Immune Complex Priming of the Nlrp3 Inflammasome Involves TLR and FcγR Cooperation and Is Dependent on CARD9.

Jillian P Rhoads, John R Lukens, Ashley J Wilhelm, Jared L Moore, Yanice Mendez-Fernandez, Thirumala-Devi Kanneganti, Amy S Major

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

60 citing papers in PubMed, 104 citations in OpenAlex.

  1. Review
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  3. IL-1 family cytokines in inflammation and immunity.Cellular & molecular immunology · 2025
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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

7 authors at 6 institutions in 1 country.

Jillian P RhoadsTennessee Valley Healthcare System, U.S. Department of Veterans Affairs, Nashville, TN 37212.
John R LukensCenter for Brain Immunology and Glia, Department of Neuroscience, University of Virginia, Charlottesville, VA 22908.
Ashley J WilhelmDivision of Rheumatology, Department of Medicine, Vanderbilt Medical Center, Nashville, TN 37232.
Jared L MooreTennessee Valley Healthcare System, U.S. Department of Veterans Affairs, Nashville, TN 37212.
Yanice Mendez-FernandezDepartment of Biology, Trevecca Nazarene University, Nashville, TN 37210; and.
Thirumala-Devi KannegantiDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105.
Amy S MajorTennessee Valley Healthcare System, U.S. Department of Veterans Affairs, Nashville, TN 37212; amy.major@vanderbilt.edu.
Vanderbilt University Medical Center · USSt. Jude Children's Research Hospital · USTrevecca Nazarene University · USUnited States Department of Veterans Affairs · USUniversity of Virginia · USVA Tennessee Valley Healthcare System · US

Funding

Interdisciplinary Training in Rheumatic DiseasesT32AR059039 · NIAMS · VANDERBILT UNIVERSITY · PI Tracy Minan Frech, AMY S MAJOR · 2010 to 2026
$4.3M
HDL-mediated transfer of mircroRNA regulates autoimmunityR21AR066971 · NIAMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MAJOR, AMY S, VICKERS, KASEY C · 2014 to 2015
$380k
Oxidized Low Density Lipoprotein Immune Complexes in AtherosclerosisF31HL128040 · NHLBI · VANDERBILT UNIVERSITY · PI RHOADS, JILLIAN PATRICIA · 2015 to 2016
$56k
oxLDL immune complex-mediated modulation of atherosclerosisI01BX002968 · VA · VETERANS HEALTH ADMINISTRATION · PI MAJOR, AMY S · 2016 to 2019
–
BLRD VA I01 BX002968NHLBI NIH HHS F31 HL128040NIAMS NIH HHS R21 AR066971NIAMS NIH HHS T32 AR059039
6 · The paper itself

Abstract

Oxidized low-density lipoprotein (oxLDL) is known to activate inflammatory responses in a variety of cells, especially macrophages and dendritic cells. Interestingly, much of the oxLDL in circulation is complexed to Abs, and these resulting immune complexes (ICs) are a prominent feature of chronic inflammatory disease, such as atherosclerosis, type-2 diabetes, systemic lupus erythematosus, and rheumatoid arthritis. Levels of oxLDL ICs often correlate with disease severity, and studies demonstrated that oxLDL ICs elicit potent inflammatory responses in macrophages. In this article, we show that bone marrow-derived dendritic cells (BMDCs) incubated with oxLDL ICs for 24 h secrete significantly more IL-1β compared with BMDCs treated with free oxLDL, whereas there was no difference in levels of TNF-α or IL-6. Treatment of BMDCs with oxLDL ICs increased expression of inflammasome-related genes

Indexed as

AnimalsAntibodiesAntigen-Antibody ComplexCARD Signaling Adaptor ProteinsCells, CulturedCytokinesDendritic CellsInflammasomesInflammation MediatorsLipoproteins, LDLMacrophagesMiceMice, Inbred C57BLNLR Family, Pyrin Domain-Containing 3 ProteinReceptor Cross-TalkReceptors, IgGAntibodiesAntigen-Antibody ComplexCard9 protein, mouseCARD Signaling Adaptor ProteinsCytokinesInflammasomesInflammation MediatorsLipoproteins, LDLNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseReceptors, IgGToll-Like Receptors

Identifiers

PMID28130494
PMCPMC5318843
OpenAlexW2581608204

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.