Evidence map›Paper›PMID 24282294›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Deletion of microRNA-155 reduces autoantibody responses and alleviates lupus-like disease in the Fas(lpr) mouse.

To-Ha Thai, Heide Christine Patterson, Duc-Hung Pham, Katalin Kis-Toth, Denise A Kaminski, George C Tsokos

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
9.8field-weighted citation impact, top 1% 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

61 citing papers in PubMed, 90 citations in OpenAlex.

  1. Review
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  4. Article
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  6. Article
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  8. Review
  9. Article
  10. MicroRNA-regulated B cells in obesity.Immunometabolism (Cobham, Surrey) · 2022
    Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. An update on epigenetic regulation in autoimmune diseases.Journal of translational autoimmunity · 2022
    Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Review

1 more citing papers are in PubMed but not listed here.

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

6 authors at 4 institutions in 3 countries.

To-Ha ThaiDepartment of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115.
Heide Christine Patterson
Duc-Hung Pham
Katalin Kis-Toth
Denise A Kaminski
George C Tsokos
Beth Israel Deaconess Medical Center · USHarvard University · USKlinikum rechts der Isar · DEUniversity of Rochester · US

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Ramnik J Xavier · 1991 to 2026
$35.3M
LYMPHOCYTE SIGNALING DEFECTS IN PATIENTS WITH LUPUSR01AI042269 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI TSOKOS, GEORGE C · 1998 to 2017
$6.8M
Syk in Mitochondrial Stress Signaling and Insulin ResistanceK08GM102718 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI PATTERSON, HEIDE CHRISTINE · 2012 to 2015
$800k
Regulation of chromatin modifications by miRNAs to control cytokine expressionR56AI099012 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI THAI, TO-HA · 2012 to 2012
$435k
NIAID NIH HHS AI099012NIAID NIH HHS AI42269NIAID NIH HHS R01 AI042269NIAID NIH HHS R56 AI099012NIDDK NIH HHS P30 DK043351NIGMS NIH HHS K08 GM102718
6 · The paper itself

Abstract

MicroRNA-155 (miR-155) regulates antibody responses and subsequent B-cell effector functions to exogenous antigens. However, the role of miR-155 in systemic autoimmunity is not known. Using the death receptor deficient (Fas(lpr)) lupus-prone mouse, we show here that ablation of miR-155 reduced autoantibody responses accompanied by a decrease in serum IgG but not IgM anti-dsDNA antibodies and a reduction of kidney inflammation. MiR-155 deletion in Fas(lpr) B cells restored the reduced SH2 domain-containing inositol 5'-phosphatase 1 to normal levels. In addition, coaggregation of the Fc γ receptor IIB with the B-cell receptor in miR-155(-/-)-Fas(lpr) B cells resulted in decreased ERK activation, proliferation, and production of switched antibodies compared with miR-155 sufficient Fas(lpr) B cells. Thus, by controlling the levels of SH2 domain-containing inositol 5'-phosphatase 1, miR-155 in part maintains an activation threshold that allows B cells to respond to antigens.

Indexed as

AnimalsAutoantibodiesBlotting, NorthernBlotting, WesternEnzyme-Linked Immunosorbent AssayFluorescent Antibody TechniqueGene DeletionHistological TechniquesImmunohistochemistryLupus Erythematosus, SystemicMiceMice, KnockoutMicroRNAsUrinalysisAutoantibodiesMicroRNAsMIRN155 microRNA, humanERK pathwaysSHIP-1

Identifiers

PMID24282294
PMCPMC3864325
OpenAlexW1986925279

What OpenQuestion holds

Textmetadata
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.