Evidence map›Paper›PMID 21828128›Full record

ArticleBlood2011

Cell-intrinsic role for IFN-α-STAT1 signals in regulating murine Peyer patch plasmacytoid dendritic cells and conditioning an inflammatory response.

Haiyan S Li, Alexander Gelbard, Gustavo J Martinez, Eiji Esashi, Huiyuan Zhang, Hoainam Nguyen-Jackson, Yong-Jun Liu, Willem W Overwijk, Stephanie S Watowich

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

39 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Review
  3. Immunomodulatory activity of heat-killedFood science & nutrition · 2024
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  5. Review
  6. Article
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  9. Article
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  14. Article
  15. IL-4 and IL-13 Guide Early Thymic Progenitors To Mature toward Dendritic Cells.Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  16. Article
  17. Review
  18. Review
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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

9 authors at 2 institutions in 2 countries.

Haiyan S LiDepartment of Immunology and Center for Inflammation and Cancer, University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Alexander Gelbard
Gustavo J Martinez
Eiji Esashi
Huiyuan Zhang
Hoainam Nguyen-Jackson
Yong-Jun Liu
Willem W Overwijk
Stephanie S Watowich
Melanoma Institute Australia · AUThe University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Molecular Mechanisms of pDC InteractionsP01CA128913 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HWU, PATRICK · 2008 to 2012
$9.3M
Training Program in Cancer ImmunobiologyT32CA009598 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ALLISON, JAMES P · 1988 to 2014
$4.9M
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
Research Training in Otolaryngology Head &Neck SurgeryT32DC007367 · NIDCD · BAYLOR COLLEGE OF MEDICINE · PI BROWNELL, WILLIAM E · 2005 to 2009
$382k
NCI NIH HHS CA128913NCI NIH HHS P01 CA128913NCI NIH HHS P30 CA016672NCI NIH HHS P30CA16672NCI NIH HHS T32 CA009598NCI NIH HHS T32-CA-09598-16NIAID NIH HHS AI059718NIAID NIH HHS AI073587NIAID NIH HHS R01 AI059718NIAID NIH HHS R21 AI073587NIAMS NIH HHS AR059010NIAMS NIH HHS RC2 AR059010NIDCD NIH HHS T32 DC007367NIDCD NIH HHS T32DC007367
6 · The paper itself

Abstract

Plasmacytoid dendritic cells (pDCs) reside in bone marrrow and lymphoid organs in homeostatic conditions and typically secrete abundant quantities of type I interferons (IFNs) on Toll-like receptor triggering. Recently, a pDC population was identified within Peyer patches (PPs) of the gut that is distinguished by its lack of IFN production; however, the relationship of PP pDCs to pDCs in other organs has been unclear. We report that PP pDCs are derived from common DC progenitors and accumulate in response to Fms-like tyrosine kinase 3 ligand, yet appear divergent in transcription factor profile and surface marker phenotype, including reduced E2-2 and CCR9 expression. Type I IFN signaling via STAT1 has a cell-autonomous role in accrual of PP pDCs in vivo. Moreover, IFN-α enhances pDC generation from DC progenitors by a STAT1-dependent mechanism. pDCs that have been developed in the presence of IFN-α resemble PP pDCs, produce inflammatory cytokines, stimulate Th17 cell generation, and fail to secrete IFN-α on Toll-like receptor engagement. These results indicate that IFN-α influences the development and function of pDCs by inducing emergence of an inflammatory (Th17-inducing) antigen-presenting subset, and simultaneously regulating accumulation of pDCs in the intestinal microenvironment.

Indexed as

AnimalsCell DifferentiationDendritic Cellsfms-Like Tyrosine Kinase 3Interferon-alphaMiceMice, Inbred C57BLPeyer's PatchesSTAT1 Transcription FactorStem CellsTh17 Cellsfms-Like Tyrosine Kinase 3Interferon-alphaStat1 protein, mouseSTAT1 Transcription Factor

Identifiers

PMID21828128
PMCPMC3193265
OpenAlexW2063341315

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.