Evidence map›Paper›PMID 23159786›Full record

ArticleClinical immunology (Orlando, Fla.)2013

The role of microparticles in the generation of immune complexes in murine lupus.

Anirudh J Ullal, David S Pisetsky

Abstract read
In one paragraph

Article in Clinical immunology (Orlando, Fla.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Article
  2. The binding of SLE autoantibodies to mitochondria.Clinical immunology (Orlando, Fla.) · 2020
    Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
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

2 authors.

Anirudh J UllalDuke University Medical Center, Department of Medicine, Durham, NC 27705, USA. anirudh.ullal@duke.edu
David S Pisetsky

Funding

Supplement - Inflammatory Triggers in B Cell AutoimmunityU19AI056363 · NIAID · DUKE UNIVERSITY · PI ST. CLAIR, EUGENE WILLIAM · 2003 to 2017
$35.3M
NIAID NIH HHS 5U19-AI-056363NIAID NIH HHS U19 AI056363
6 · The paper itself

Abstract

Systemic lupus erythematosus is a systemic inflammatory disease characterized by antibodies to nuclear molecules in association with immune complex deposition. As shown previously, microparticles (MPs), which are small membrane-bound vesicles released from dying and activated cells, contain nucleic acids and can form immune complexes found in patient blood. To assess the role of MPs in murine lupus, we used flow cytometry to measure the presence of MPs with bound IgG in the blood of MRL-lpr/lpr and NZB/W mice. These studies showed much higher numbers of MPs with bound IgG in the blood of MRL lpr/lpr compared to NZB/W mice. Furthermore, these studies showed that antibodies from MRL-lpr/lpr mice bound better to MPs from apoptotic cells than those from NZB/W mice. Together, these studies indicate important differences in the serological features of the two strains as reflected by the capacity of antibodies to bind to MPs.

Indexed as

AnimalsAntibodies, AntinuclearAntigen-Antibody ComplexApoptosisCell-Derived MicroparticlesCell LineEnzyme-Linked Immunosorbent AssayFlow CytometryHL-60 CellsHumansImmunoglobulin GJurkat CellsLupus Erythematosus, SystemicMiceMice, Inbred BALB CMice, Inbred MRL lprAntibodies, AntinuclearAntigen-Antibody ComplexImmunoglobulin G

Identifiers

PMID23159786
PMCPMC3551532

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Registered trials

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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.