Evidence map›Paper›PMID 24416644›Full record

ReviewJAK-STAT2013

Diversification of dendritic cell subsets: Emerging roles for STAT proteins.

Haiyan S Li, Stephanie S Watowich

Open access · bronzeAbstract readReview
In one paragraph

Review in JAK-STAT, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Contribution of Dendritic Cell Subsets to T Cell-Dependent Responses in Mice.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. STAT3 signaling in immunity.Cytokine & growth factor reviews · 2016
    Review
  14. Article
  15. Immunological Consequences of JAK Inhibition: Friend or Foe?Current hematologic malignancy reports · 2015
    Review
  16. Article
  17. Article
  18. Review
  19. 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

2 authors at 1 institution in 1 country.

Haiyan S LiDepartment of Immunology; The University of Texas MD Anderson Cancer Center; Houston, TX USA.
Stephanie S WatowichDepartment of Immunology; The University of Texas MD Anderson Cancer Center; Houston, TX USA ; The University of Texas Graduate School of Biomedical Sciences; Houston, TX USA.
The University of Texas MD Anderson Cancer Center · US

Funding

Pathways regulating plasmacytoid dendritic cells in Peyers PatchesR21AI098099 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI WATOWICH, STEPHANIE S · 2012 to 2013
$435k
NIAID NIH HHS R21 AI098099
6 · The paper itself

Abstract

The term dendritic cell (DC) refers to a population of hematopoietic cells with critical roles in immunity, including immune activation in response to pathogen-elicited danger signals and immune tolerance. Aberrant DC activity is an important contributing factor in autoimmunity, while severe DC depletion accompanies certain immunodeficiency conditions. By contrast, DCs have become attractive candidates to manipulate in immune therapy. Recent studies show that STAT transcription factors have unique roles in DCs, a feature that might be exploited in future DC-based therapies. Here, we focus on the functions of STAT1, STAT3, and STAT5 in DC generation and DC-mediated immune responses.

Indexed as

cytokinesdendritic cellsimmune cell developmentSTAT proteins

Identifiers

PMID24416644
PMCPMC3876424
OpenAlexW2028911106

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.