Evidence map›Paper›PMID 23303674›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Cutting edge: Type I IFN drives emergency myelopoiesis and peripheral myeloid expansion during chronic TLR7 signaling.

Matthew B Buechler, Thomas H Teal, Keith B Elkon, Jessica A Hamerman

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

57 citing papers in PubMed, 75 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Immune Mechanisms in Inflammatory Anemia.Annual review of immunology · 2023
    Review
  11. Review
  12. Article
  13. OralFrontiers in cellular and infection microbiology · 2022
    Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. B Cell αv Integrins Regulate TLR-Driven Autoimmunity.Journal of immunology (Baltimore, Md. : 1950) · 2020
    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

4 authors at 2 institutions in 1 country.

Matthew B BuechlerDepartment of Immunology, University of Washington, Seattle, WA 98195, USA.
Thomas H Teal
Keith B Elkon
Jessica A Hamerman
University of Washington · USBenaroya Research Institute

Funding

BASIC IMMUNOLOGYT32CA009537 · NCI · UNIVERSITY OF WASHINGTON · PI GOVERMAN, JOAN M · 1986 to 2012
$3.1M
Apoptotic Cells As Immunogens In SLER01AR048796 · NIAMS · UNIVERSITY OF WASHINGTON · PI ELKON, KEITH B. · 2001 to 2010
$2.7M
Regulation of Inflammatory Signaling during the Innate Immune ResponseR01AI073441 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI HAMERMAN, JESSICA A · 2007 to 2011
$2.4M
Regulation of dendritic cell inflammatory responsesR01AI081948 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI HAMERMAN, JESSICA A · 2010 to 2014
$2.2M
Regulation of TSLP-Mediated Skin InflammationR01AR055695 · NIAMS · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI CAMPBELL, DANIEL J, HAMERMAN, JESSICA A · 2009 to 2013
$2.0M
NCI NIH HHS T32 CA009537NCI NIH HHS T32CA009537NIAID NIH HHS R01 AI073441NIAID NIH HHS R01 AI081948NIAMS NIH HHS AR48796NIAMS NIH HHS R01 AR048796NIAMS NIH HHS R01 AR055695
6 · The paper itself

Abstract

Mice overexpressing TLR7 (TLR7.1 mice) are a model of systemic lupus erythematosus pathogenesis and exhibit peripheral myeloid expansion. We show that TLR7.1 mice have a dramatic expansion of splenic cells that derive from granulocyte/macrophage progenitors (GMP) compared with wild-type mice. In the bone marrow, TLR7.1 mice exhibited hallmarks of emergency myelopoiesis and contained a discrete population of Sca-1(+) GMP, termed emergency GMP, which are more proliferative and superior myeloid precursors than classical Sca-1(-) GMP. The emergency myelopoiesis and peripheral myeloid expansion in TLR7.1 mice was dependent on type I IFN signaling. TLR7 agonist administration to nontransgenic mice also drove type I IFN-dependent emergency myelopoiesis. TLR7.1 plasmacytoid dendritic cells were cell-intrinsically activated by TLR7 overexpression and constitutively produced type I IFN mRNA. This study shows that type I IFN can act upon myeloid progenitors to promote the development of emergency GMP, which leads to an expansion of their progeny in the periphery.

Indexed as

AnimalsAntigens, LyBone MarrowCell DivisionCell LineageDendritic CellsDisease Models, AnimalGene Expression RegulationGranulocytesInterferon Type ILupus Erythematosus, SystemicMacrophagesMembrane GlycoproteinsMembrane ProteinsMiceMice, TransgenicAntigens, LyIfnar1 protein, mouseInterferon Type ILy6a protein, mouseMembrane GlycoproteinsMembrane ProteinsReceptor, Interferon alpha-betaRNA, MessengerTlr7 protein, mouseToll-Like Receptor 7

Identifiers

PMID23303674
PMCPMC3552021
OpenAlexW2139527574

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.