Evidence map›Paper›PMID 19660813›Full record

ArticleMolecular immunology2009

Augmenting DAF levels in vivo ameliorates experimental autoimmune encephalomyelitis.

Qing Li, Danping Huang, Kristine Nacion, Hong Bu, Feng Lin

Abstract read
In one paragraph

Article in Molecular 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 41% 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, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Overexpression of Decay Accelerating Factor Mitigates Fibrotic Responses to Lung Injury.American journal of respiratory cell and molecular biology · 2022
    Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. CD318 is a ligand for CD6.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  9. CD6 as a potential target for treating multiple sclerosis.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  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

5 authors at 2 institutions in 2 countries.

Qing LiInstitute of Pathology, Case Western Reserve University, Cleveland, OH, USA.
Danping Huang
Kristine Nacion
Hong Bu
Feng Lin
Case Western Reserve University · USWest China Hospital of Sichuan University · CN

Funding

TISSUE CULTURE AND HYBRIDOMA MODULEP30EY011373 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI Irina A Pikuleva · 1997 to 2026
$17.7M
Synergy between T cells and Complement in EAER01NS052471 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI LIN, FENG C · 2005 to 2010
$1.3M
NEI NIH HHS EY11373NEI NIH HHS P30 EY011373NINDS NIH HHS NS052471NINDS NIH HHS R01 NS052471
6 · The paper itself

Abstract

Recent studies in experimental autoimmune encephalomyelitis (EAE) have found that CNS injury in Daf1(-/-) mice is much greater than in wild types (WTs), suggesting that upregulating DAF levels in vivo might ameliorate disease. To test this, we generated a Daf1 transgenic (Tg) mouse which had elevated DAF levels on its cell surfaces. In by-stand C3b uptake assays, Daf1 Tg mouse erythrocytes took up less C3b on their surfaces than WT erythrocytes. When co-cultured with OT-II CD4(+) T cells together with OVA(323-339) peptide, Daf1 Tg mouse bone marrow derived dendritic cells (BM-DCs) produced less C5a and C3a than WT BM-DCs and stimulated a lesser T cell response. In MOG(35-55) immunization induced EAE model, Daf1 Tg mice exhibited delayed disease onset and decreased clinical scores compared to WTs. Histological analyses showed that there were less inflammation and demyelination in spinal cords in Daf1 Tg mice than those in WTs. In accordance with these results, Daf1 Tg mice had decreased MOG(35-55) specific Th1 and Th17 responses. These data provide further evidence that DAF suppresses autoreactive T cell responses in EAE, and indicate that augmenting its expression levels could be effective therapeutically in treating multiple sclerosis as well as other T cell mediated diseases.

Indexed as

AnimalsCD55 AntigensComplement C3aComplement C5aDendritic CellsDisease Models, AnimalEncephalomyelitis, Autoimmune, ExperimentalErythrocytesGlycoproteinsInterferon-gammaInterleukin-17Lymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicCD55 AntigensComplement C3aComplement C5adecay-accelerating factor 1, mouseGlycoproteinsInterferon-gammaInterleukin-17Myelin-Oligodendrocyte Glycoproteinmyelin oligodendrocyte glycoprotein (35-55)OVA 323-339OvalbuminPeptide Fragments

Identifiers

PMID19660813
PMCPMC2753188
OpenAlexW2131283448

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.