Evidence map›Paper›PMID 18832727›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

Stat4 isoforms differentially regulate inflammation and demyelination in experimental allergic encephalomyelitis.

Caiqing Mo, Wanida Chearwae, John T O'Malley, Suzanne M Adams, Saravanan Kanakasabai, Crystal C Walline, Gretta L Stritesky, Seth R Good, Narayanan B Perumal, Mark H Kaplan and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 44 citations in OpenAlex.

  1. Trial
  2. An IL-23-STAT4 pathway is required for the proinflammatory function of classical dendritic cells during CNS inflammation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. The Exposure to Lead (Pb) Exacerbates Immunological Abnormalities in BTBR TInternational journal of molecular sciences · 2023
    Article
  4. Article
  5. Review
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  10. Review
  11. Th17 cells demonstrate stable cytokine production in a proallergic environment.Journal of immunology (Baltimore, Md. : 1950) · 2014
    Article
  12. Article
  13. Article
  14. Opposing roles of STAT4 and Dnmt3a in Th1 gene regulation.Journal of immunology (Baltimore, Md. : 1950) · 2013
    Article
  15. Article
  16. Article
  17. Review
  18. Article
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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

11 authors at 3 institutions in 1 country.

Caiqing MoNeuroscience Research Laboratory, Methodist Research Institute, Indianapolis, IN 46202, USA.
Wanida Chearwae
John T O'Malley
Suzanne M Adams
Saravanan Kanakasabai
Crystal C Walline
Gretta L Stritesky
Seth R Good
Narayanan B Perumal
Mark H Kaplan
John J Bright
IST Research · USIndiana University School of MedicineUniversity of Indianapolis · US

Funding

STAT4 IMMUNOLOGYR01AI045515 · NIAID · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI KAPLAN, MARK H · 1999 to 2014
$4.3M
PPAR-gamma regulation of IL-12 in CNS demyelinationR01NS042257 · NINDS · VANDERBILT UNIVERSITY · PI BRIGHT, JOHN J · 2003 to 2005
$675k
Stat4 ImmunobiologyR56AI045515 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI KAPLAN, MARK H · 2009 to 2009
$385k
NIAID NIH HHS AI045515NIAID NIH HHS R01 AI045515NIAID NIH HHS R56 AI045515NINDS NIH HHS R01 NS042257NINDS NIH HHS R01 NS42257
6 · The paper itself

Abstract

Experimental allergic encephalomyelitis (EAE) is a T cell-mediated autoimmune disease model of multiple sclerosis. Signal transducer and activator of transcription 4 (Stat4) is a transcription factor activated by IL-12 and IL-23, two cytokines known to play important roles in the pathogenesis of EAE by inducing T cells to secrete IFN-gamma and IL-17, respectively. We and others have previously shown that therapeutic intervention or targeted disruption of Stat4 was effective in ameliorating EAE. Recently, a splice variant of Stat4 termed Stat4beta has been characterized that lacks 44 amino acids at the C terminus of the full-length Stat4alpha. In this study we examined whether T cells expressing either isoform could affect the pathogenesis of EAE. We found that transgenic mice expressing Stat4beta on a Stat4-deficient background develop an exacerbated EAE compared with wild-type mice following immunization with myelin oligodendrocyte glycoprotein peptide 35-55, while Stat4alpha transgenic mice have greatly attenuated disease. The differential development of EAE in transgenic mice correlates with increased IFN-gamma and IL-17 in Stat4beta-expressing cells in situ, contrasting increased IL-10 production by Stat4alpha-expressing cells. This study demonstrates that Stat4 isoforms differentially regulate inflammatory cytokines in association with distinct effects on the onset and severity of EAE.

Indexed as

Amino Acid SequenceAnimalsEncephalomyelitis, Autoimmune, ExperimentalGene Expression RegulationGlycoproteinsInflammationInterferon-gammaInterleukin-10Interleukin-12Interleukin-17Interleukin-23MiceMice, KnockoutMultiple SclerosisMyelin-Oligodendrocyte GlycoproteinPeptide FragmentsGlycoproteinsInterferon-gammaInterleukin-10Interleukin-12Interleukin-17Interleukin-23Myelin-Oligodendrocyte Glycoproteinmyelin oligodendrocyte glycoprotein (35-55)Peptide FragmentsProtein IsoformsStat4 protein, mouseSTAT4 Transcription Factor

Identifiers

PMID18832727
PMCPMC2581484
OpenAlexW2137766212

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.