Evidence map›Paper›PMID 21282039›Full record

ArticleJournal of autoimmunity2011

IL-2: a two-faced master regulator of autoimmunity.

Rahul Sharma, Shu Man Fu, Shyr-Te Ju

Abstract read
In one paragraph

Article in Journal of autoimmunity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Regulatory T cells in acute and chronic kidney diseases.American journal of physiology. Renal physiology · 2018
    Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Cytokines in the Germinal Center Niche.Antibodies (Basel, Switzerland) · 2016
    Review
  15. Article
  16. Article
  17. Article
  18. The autoimmune side of heart and lung diseases.Clinical reviews in allergy & immunology · 2013
    Review
  19. Review
  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

3 authors at 2 institutions in 1 country.

Rahul SharmaCenter for Immunity, Inflammation and Regenerative Medicine, Department of Medicine, University of Virginia, VA, USA.
Shu Man Fu
Shyr-Te Ju
Center for Neuroscience and Regenerative Medicine · USUniversity of Virginia · US

Funding

Cellular and Genetic Basis of Systemic LupusR01AR047988 · NIAMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI FU, SHU MAN · 2001 to 2020
$8.4M
HLA-D Region Systemic Lupus Erythematosus PathogenesisR01AR049449 · NIAMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI FU, SHU MAN · 2005 to 2015
$4.2M
Regulatory T Cell-Deficient Mouse Model Rapidly Develops Sjogren's SyndromeR01DE017570 · NIDCR · UNIVERSITY OF VIRGINIA · PI JU, SHYR-TE · 2006 to 2010
$1.7M
End Organ Failure Controlled by IL-2 and FasR01AR051203 · NIAMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI JU, SHYR-TE · 2005 to 2009
$1.6M
NIAMS NIH HHS AR-047988NIAMS NIH HHS AR-049449NIAMS NIH HHS AR-051203NIAMS NIH HHS R01 AR047988NIAMS NIH HHS R01 AR049449NIAMS NIH HHS R01 AR051203NIDCR NIH HHS DE-01759NIDCR NIH HHS R01 DE017570
6 · The paper itself

Abstract

CD4(+) T-cell (Th) cytokines provide important regulatory and effector functions of T-cells. Among them, IL-2 plays a unique role. IL-2 is required for the generation and maintenance of regulatory T-cells (Treg) to provide lifelong protection from autoimmune disease. Whether IL-2 is also required for autoimmune disease development is less clear as Il2(-/)(-) mice themselves spontaneously develop multi-organ inflammation (MOI). In this communication, we discuss evidence that support the thesis that IL-2 is required for the development of autoimmune response, although some aspects of autoimmune response are not regulated by IL-2. Potential IL-2-dependent mechanisms operating at specific stages of the inflammation process are presented. The interplays among Treg, IL-2, autoimmune response and adaptive immunity are discussed. Overall, available information indicates that IL-2 is a two-faced master regulator of autoimmunity: one to prevent autoimmunity while the other promotes autoimmune response. The latter is an unfortunate consequence of IL-2 function that is used to promote the adaptive immune response against foreign antigens and pathogens.

Indexed as

AnimalsAntigen-Presenting CellsAntigensAutoimmunityHumansInflammationInterleukin-2MiceMice, KnockoutModels, ImmunologicalT-LymphocytesT-Lymphocytes, RegulatoryAntigensInterleukin-2

Identifiers

PMID21282039
PMCPMC3046218
OpenAlexW2056745378

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.