Evidence map›Paper›PMID 19031437›Full record

ArticleGlia2009

Treatment with selective estrogen receptor modulators regulates myelin specific T-cells and suppresses experimental autoimmune encephalomyelitis.

Bruce F Bebo, Babak Dehghani, Scott Foster, Astrid Kurniawan, Francisco J Lopez, Larry S Sherman

Registry-linked trialAbstract read
In one paragraph

Article in Glia, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02710214 (Effect of a Tissue Selective Estrogen Complex on Menopausal Symptoms in Women With MS), which is not on this map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.2field-weighted citation impact, top 12% 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.

NCT02710214 phase2completednot on this mapstarted 2016, after this paper: background citation

Effect of a Tissue Selective Estrogen Complex on Menopausal Symptoms in Women With MS: A Pilot Trial.

TypeinterventionalSponsorUniversity of California, San FranciscoRan2016 to 2019Enrolled24ConditionsMenopause, Multiple SclerosisArmsTissue Selective Estrogen Complex, Placebo
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Effects of the Menstrual Cycle on Neurological Disorders.Current neurology and neuroscience reports · 2021
    Review
  15. The immunomodulatory effects of endocrine therapy in breast cancer.Journal of experimental & clinical cancer research : CR · 2021
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Observational
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 3 institutions in 1 country.

Bruce F BeboNeurological Sciences Institute, Oregon Health & Science University, Beaverton, Oregon, USA.
Babak Dehghani
Scott Foster
Astrid Kurniawan
Francisco J Lopez
Larry S Sherman
Oregon Health & Science University · USLigand Pharmaceuticals (United States) · USOregon National Primate Research Center · US

Funding

Effects of hyaluronan on neural stem cell homing and differentiationR01NS056234 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI SHERMAN, LARRY S. · 2006 to 2008
$960k
Phytoestrogens as an alternative treatment for MSR01AT001517 · NCCIH · OREGON HEALTH & SCIENCE UNIVERSITY · PI SHERMAN, LARRY S. · 2003 to 2006
$793k
Suppression of EAE by placentally derived glycoproteinR21NS047418 · NINDS · OREGON HEALTH AND SCIENCE UNIVERSITY · PI SHERMAN, LARRY S. · 2004 to 2005
$384k
NCCIH NIH HHS R01 AT001517NINDS NIH HHS R01 NS056234NINDS NIH HHS R21 NS047418
6 · The paper itself

Abstract

Steroidal estrogens can regulate inflammatory immune responses and may be involved in the suppression of multiple sclerosis (MS) during pregnancy. However, the risks and side effects associated with steroidal estrogens may limit their usefulness for long-term MS therapy. Selective estrogen receptor modulators (SERMs) could provide an alternative therapeutic strategy, because they behave as estrogen agonists in some tissues, but are either inert or behave like estrogen antagonists in other tissues. In this study, we investigated the ability of two commercially available SERMs (tamoxifen and raloxifene) to regulate myelin specific immunity and experimental autoimmune encephalomyelitis (EAE) in mice. Both tamoxifen and raloxifene suppressed myelin antigen specific T-cell proliferation. However, tamoxifen was more effective in this regard. Tamoxifen treatment reduced the induction of major histocompatibility complex II by lipopolysaccharide stimulated dendritic cells and decreased their ability to activate myelin specific T-cells. At lower doses, tamoxifen was found to increase the levels of Th2 transcription factors and induce a Th2 bias in cultures of myelin-specific splenocytes. EAE symptoms and the degree of demyelination were less severe in mice treated with tamoxifen than in control mice. These findings support the notion that tamoxifen or related SERMs are potential agents that could be used in the treatment of inflammatory autoimmune disorders that affect the central nervous system.

Indexed as

AnimalsCell ProliferationCells, CulturedDemyelinating DiseasesDendritic CellsEncephalomyelitis, Autoimmune, ExperimentalEstrogen Receptor alphaFemaleGenes, MHC Class IIImmunity, CellularLipopolysaccharidesMiceMice, KnockoutMice, TransgenicMyelin ProteinsMyelin SheathEstrogen Receptor alphaLipopolysaccharidesMyelin ProteinsRaloxifene HydrochlorideSelective Estrogen Receptor ModulatorsTamoxifen

Identifiers

PMID19031437
PMCPMC2667209
OpenAlexW2048944834

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.