Evidence map›Paper›PMID 18362339›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2008

Amino acid copolymer-specific IL-10-secreting regulatory T cells that ameliorate autoimmune diseases in mice.

Joel N H Stern, Derin B Keskin, Hong Zhang, Huijuan Lv, Zenichiro Kato, Jack L Strominger

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Genetically modified hematopoietic stem/progenitor cells that produce IL-10-secreting regulatory T cells.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  5. Article
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  9. Cannabinoids decrease the th17 inflammatory autoimmune phenotype.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2013
    Article
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  13. Review
  14. Review
  15. Article
  16. Promoting tolerance to proteolipid protein-induced experimental autoimmune encephalomyelitis through targeting dendritic cells.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  17. CNS expression of anti-inflammatory cytokine interleukin-4 attenuates Alzheimer's disease-like pathogenesis in APP+PS1 bigenic mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2010
    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

6 authors at 1 institution in 1 country.

Joel N H SternDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA. jstern@fas.harvard.edu
Derin B Keskin
Hong Zhang
Huijuan Lv
Zenichiro Kato
Jack L Strominger
Harvard University · US

Funding

MHC proteins, copolymers and peptide 15mers in EAER01AI049524 · NIAID · HARVARD UNIVERSITY · PI STROMINGER, JACK L · 2001 to 2010
$5.7M
NIAID NIH HHS 5R01 AI049524NIAID NIH HHS R01 AI049524
6 · The paper itself

Abstract

IL-10-secreting regulatory T cell lines specific to glatiramer acetate [poly(Y,E,A,K)n] or poly(Y,F,A,K)n have been established from the enlarged spleen and lymph nodes that result from copolymer treatment of SJL mice in which experimental autoimmune encephalomyelitis was induced by PLP139-151. These CD4+CD25+T cell lines secrete high levels of IL-10 and IL-13 but only small amounts of IL-4 and virtually no TGF-beta, IL-17, IL-6, IFN-gamma, or TNF-alpha. Their phenotypes are particularly characterized by the absence of Foxp3 and the presence of two TNFR family members, CD30 and GITR. The lines proliferated specifically to the immunizing copolymers but were autoantigen-nonspecific, in that the same T cell line could suppress autoimmunity induced by three different autoantigens in SJL mice, i.e., PLP139-151(EAE), MBP85-99 (EAE), and bovine peripheral nerve myelin (experimental autoimmune neuritis), indicating they function by bystander suppression.

Indexed as

Adoptive TransferAmino AcidsAnimalsBystander EffectCattleCell LineCell ProliferationCell SeparationEncephalomyelitis, Autoimmune, ExperimentalForkhead Transcription FactorsInterleukin-10MicePeptidesPhenotypeReceptors, Antigen, T-CellT-Lymphocytes, RegulatoryAmino AcidsForkhead Transcription FactorsFoxp3 protein, mouseInterleukin-10PeptidesReceptors, Antigen, T-Cell

Identifiers

PMID18362339
PMCPMC2278190
OpenAlexW2057821000

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.