Evidence map›Paper›PMID 19850149›Full record

ReviewThe international journal of biochemistry & cell biology2010

Forkhead transcription factors in chronic inflammation.

Stanford L Peng

Abstract readReview
In one paragraph

Review in The international journal of biochemistry & cell biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

27 citing papers in PubMed, 49 citations in OpenAlex.

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  14. Frontiers in pharmacology · 2021
    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

1 author at 1 institution in 1 country.

Stanford L PengVirginia Mason Medical Center and Benaroya Research Institute, 1100 Ninth Ave., X6-RHE, Seattle, WA 98101, USA. stanford.peng@vmmc.org <stanford.peng@vmmc.org>
Benaroya Research Institute

Funding

Forkhead transcription factors in T lymphocytesR01AI061478 · NIAID · WASHINGTON UNIVERSITY · PI HSIEH, CHYI S · 2004 to 2008
$1.7M
Molecular mechanisms of autoreactive B cell activationR01AI057471 · NIAID · WASHINGTON UNIVERSITY · PI DAL PORTO, JOSEPH · 2004 to 2008
$1.4M
NIAID NIH HHS R01 AI057471NIAID NIH HHS R01 AI061478
6 · The paper itself

Abstract

Forkhead (Fox) transcription factors have been increasingly recognized to play key roles in immune homeostasis, especially Foxp3 for its role in the development and function of regulatory T cells, and Foxo family members for their regulatory role in T and B lymphocytes as well as other leukocytes. Although these transcription factors positively regulate the expression of multiple target genes, a unique functional attribute of these genes is the maintenance of leukocyte homeostasis, such as the preservation of the naïve or quiescent T cell state and prevention of autoimmunity. As a result, many chronic inflammatory processes appear to reflect a relative loss of activity of one of these transcription factors, raising the possibility that therapeutic approaches which confer gain-of-function Fox activity may be beneficial. On the other hand, however, some of the Fox family members also appear to promote and/or maintain chronic inflammation by preserving inflammatory leukocyte survival and/or otherwise promoting the expression of inflammatory target genes, at least in some cell types such as neutrophils. Therefore, although the role of Fox in inflammatory disorders remains complex and incompletely understood, the continued study of these factors provides new insight into the initiation, maintenance, and propagation of inflammation.

Indexed as

AutoimmunityInflammationAnimalsChronic DiseaseForkhead Transcription FactorsHumansLymphocytesNeutrophilsForkhead Transcription Factors

Identifiers

PMID19850149
PMCPMC2835811
OpenAlexW2054624549

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.