Evidence map›Paper›PMID 21084088›Full record

ArticleAtherosclerosis2011

The inhibitory FcγRIIb modulates the inflammatory response and influences atherosclerosis in male apoE(-/-) mice.

Yanice V Mendez-Fernandez, Bonnie G Stevenson, Cody J Diehl, Nicole A Braun, Nekeithia S Wade, Roman Covarrubias, Sander van Leuven, Joseph L Witztum, Amy S Major

Abstract read
In one paragraph

Article in Atherosclerosis, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Atherosclerosis antigens as targets for immunotherapy.Nature cardiovascular research · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. FcγRIIb on CD11cAtherosclerosis · 2019
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Update on cardiovascular disease in lupus.Current opinion in rheumatology · 2016
    Review
  16. Fcγ Receptors in Solid Organ Transplantation.Current transplantation reports · 2016
    Review
  17. Article
  18. Review
  19. Article
  20. Article
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

9 authors at 3 institutions in 2 countries.

Yanice V Mendez-FernandezDepartment of Medicine, Vanderbilt University Medical Center, Nashville, USA. yanice.mendez@vanderbilt.edu
Bonnie G Stevenson
Cody J Diehl
Nicole A Braun
Nekeithia S Wade
Roman Covarrubias
Sander van Leuven
Joseph L Witztum
Amy S Major
Vanderbilt University Medical Center · USUniversity of California, San Diego · USAcademic Medical Center · NL

Funding

Transcriptional GenomicsP01HL088093 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WITZTUM, JOSEPH L. · 2008 to 2018
$26.4M
TRAINING GRANT IN MECHANISMS OF VASCULAR DISEASET32HL007751 · NHLBI · VANDERBILT UNIVERSITY · PI BOCK, PAUL E · 1994 to 2014
$6.6M
Role of iNKT Cells in Autoimmunity and AtherosclerosisR01HL089310 · NHLBI · VANDERBILT UNIVERSITY · PI MAJOR, AMY S · 2007 to 2011
$2.2M
Development of a Vaccine Approach to Inhibit AtherosclerosisR01HL086559 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WITZTUM, JOSEPH L. · 2007 to 2011
$2.0M
Accelerated Atherosclerosis and system lupus erythematosusR01HL088364 · NHLBI · VANDERBILT UNIVERSITY · PI MAJOR, AMY S · 2008 to 2011
$1.6M
NHLBI NIH HHS 5T32HL07751NHLBI NIH HHS HL088093NHLBI NIH HHS P01 HL088093NHLBI NIH HHS R01 HL086559NHLBI NIH HHS R01 HL088364NHLBI NIH HHS R01HL088364NHLBI NIH HHS R01 HL089310NHLBI NIH HHS R01HL089310NHLBI NIH HHS T32 HL007751
6 · The paper itself

Abstract

backgroundAtherosclerosis is widely accepted as an inflammatory disease involving both innate and adaptive immunity. B cells and/or antibodies have previously been shown to play a protective role against atherosclerosis. Aside from their ability to bind to antigens, antibodies can influence inflammatory responses by interacting with various Fcγ receptors on the surface of antigen presenting cells. Although studies in mice have determined that stimulatory Fcγ receptors contribute to atherosclerosis, the role of the inhibitory Fcγ receptor IIb (FcγRIIb) has only recently been investigated. METHODS AND

resultsTo determine the importance of FcγRIIb in modulating the adaptive immune response to hyperlipidemia, we generated FcγRIIb-deficient mice on the apoE-deficient background (apoE/FcγRIIb(-/-)). We report that male apoE/FcγRIIb(-/-) mice develop exacerbated atherosclerosis that is independent of lipid levels, and is characterized by increased antibody titers to modified LDL and pro-inflammatory cytokines in the aorta.

conclusionsThese findings suggest that antibodies against atherosclerosis-associated antigens partially protect against atherosclerosis in male apoE(-/-) mice by conveying inhibitory signals through the FcγRIIb that downregulate pro-inflammatory signaling via other immune receptors. These data are the first to describe a significant in vivo effect for FcγRIIb in modulating the cytokine response in the aorta in male apoE(-/-) mice.

Indexed as

AnimalsAntigen-Presenting CellsAntigensAortaApolipoproteins EAtherosclerosisB-LymphocytesCytokinesEnzyme-Linked Immunosorbent AssayInflammationLipoproteins, LDLMaleMiceMice, TransgenicReceptors, IgGAntigensApolipoproteins ECytokinesFcgr2b protein, mouseLipoproteins, LDLReceptors, IgG

Identifiers

PMID21084088
PMCPMC3052995
OpenAlexW2054943022

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.