Evidence map›Paper›PMID 19604301›Full record

ArticleImmunology2009

Inverse relationship between dendritic cell CCR9 expression and maturation state.

Maureen L Drakes, Patrick J Stiff, Thomas G Blanchard

Open access · greenAbstract read
In one paragraph

Article in Immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.2field-weighted citation impact, top 42% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. CCL25 Signaling in the Tumor Microenvironment.Advances in experimental medicine and biology · 2021
    Article
  4. Article
  5. The Regulatory Function of CCR9Frontiers in immunology · 2020
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. 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.

Maureen L DrakesDepartment of Medicine, Oncology Institute, Loyola University Chicago, Maywood, IL 60153, USA.
Patrick J Stiff
Thomas G Blanchard
Loyola University Chicago · USUniversity of Maryland, Baltimore · US

Funding

TUMOR METABOLISM PROGRAMP30CA043703 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MARK R CHANCE · 1987 to 2026
$142.3M
H. PYLORI-SPECIFIC REGULATORY T CELLS THAT LIMIT HOST RESPONSER01AI055710 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI BLANCHARD, THOMAS G · 2004 to 2008
$1.1M
Probiotic Modulation/Dendritic Cells in Experimental IBDR03DK065859 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI DRAKES, MAUREEN · 2005 to 2006
$298k
Helicobacter Pylori-Specific Regulatory T Cells that Limit the Host ResponseR56AI055710 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI BLANCHARD, THOMAS G · 2010 to 2010
$263k
NCI NIH HHS P30 CA043703NCI NIH HHS P30 CA43703NIAID NIH HHS AI-055710NIAID NIH HHS R01 AI055710NIAID NIH HHS R56 AI055710NIDDK NIH HHS DK-95859NIDDK NIH HHS R03 DK065859
6 · The paper itself

Abstract

CCR9 has been identified on T cells as a chemokine receptor that directs these cells to migrate to the intestine. CCR9 has also been reported on different cell types in the intestine, thymus, liver and peripheral blood. Little is reported concerning the presence of or functional implications of this chemokine receptor on myeloid dendritic cells (DC). In the host, DC encounter a multiplicity of antigenic stimuli to which they mount immune responses. In addition to intracellular and functional changes on sensing antigen, maturation of DC is typically reflected in the up-regulation of costimulatory molecules on DC. However, alterations in other surface markers may also be an indicator of DC activation. Using bone marrow-propagated DC these studies investigated cellular maturation in the presence of microbial stimuli and analyzed the relationship of CCR9 expression with DC maturation. Fractionation of DC into CCR9(high) and CCR9(low)subsets revealed a distinct ability of each subset to induce division in naïve CD4(+) T cells. Our results suggest that DC expressing high levels of CCR9 are less activated/mature than DC expressing low levels of CCR9.

Indexed as

AnimalsBacteriaBone Marrow CellsCell DifferentiationCell DivisionCells, CulturedColonCytokinesDendritic CellsFemaleInterleukin-2Lymphocyte ActivationMiceMice, Inbred BALB CReceptors, CCRCC chemokine receptor 9CytokinesInterleukin-2Receptors, CCR

Identifiers

PMID19604301
PMCPMC2729524
OpenAlexW2041483393

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.