Evidence map›Paper›PMID 20969586›Full record

ReviewImmunological reviews2010

Mechanisms regulating dendritic cell specification and development.

Stephanie S Watowich, Yong-Jun Liu

Abstract readReview
In one paragraph

Review in Immunological reviews, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed, 1 pooled it
–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

82 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Blocking IL-1β reverses the immunosuppression in mouse breast cancer and synergizes with anti-PD-1 for tumor abrogation.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Trial
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Dendritic Cells andMicroorganisms · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Cell death pathways and viruses: Role of microRNAs.Molecular therapy. Nucleic acids · 2021
    Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

22 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

2 authors.

Stephanie S WatowichDepartment of Immunology and Center for Cancer Immunology Research, The University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA. swatowic@mdanderson.org
Yong-Jun Liu

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Transcriptome and epigenome analysis of helper T cell specification and plasticitRC2AR059010 · NIAMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DONG, CHEN · 2009 to 2010
$2.8M
IPC Developmental Pathways and RegulationR01AI059718 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LIU, YONG-JUN · 2005 to 2009
$1.8M
Cytokine Regulation of Dendritic Cell DevelopmentR21AI073587 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI WATOWICH, STEPHANIE S · 2007 to 2008
$409k
NCI NIH HHS P30 CA016672NCI NIH HHS P30CA16672NIAID NIH HHS AI059718NIAID NIH HHS AI073587NIAID NIH HHS R01 AI059718NIAID NIH HHS R21 AI073587NIAMS NIH HHS AR059010NIAMS NIH HHS RC2 AR059010
6 · The paper itself

Abstract

Understanding the diversification of dendritic cell (DC) lineages is one of the last frontiers in mapping the developmental hierarchy of the hematopoietic system. DCs are a vital link between the innate and adaptive immune responses; thus, elucidating their developmental pathways is crucial for insight into the generation of natural immunity and for learning how to regulate DCs in clinical settings. DCs arise from hematopoietic stem cells through specialized progenitor subsets under the direction of FMS-like tyrosine kinase 3 ligand (Flt3L) and Flt3L receptor (Flt3) signaling. Recent studies have revealed important contributions from granulocyte-macrophage colony-stimulating factor (GM-CSF) and type I interferons (IFNs) in vivo. Furthermore, DC development is guided by lineage-restricted transcription factors such as IRF8, E2-2, and Batf3. A critical question centers on how cytokines and lineage-restricted transcription factors operate molecularly to direct DC diversification. Here, we review recent findings that provide new insight into the DC developmental process.

Indexed as

AnimalsCell DifferentiationCell LineageDendritic CellsGene Expression Regulation, DevelopmentalGranulocyte-Macrophage Colony-Stimulating FactorHematopoietic Stem CellsHumansImmune SystemInterferon Type IMembrane ProteinsSignal Transductionflt3 ligand proteinGranulocyte-Macrophage Colony-Stimulating FactorInterferon Type IMembrane Proteins

Identifiers

PMID20969586
PMCPMC3039024

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.