Evidence map›Paper›PMID 29574654›Full record

ArticleInflammation2018

SERMs Promote Anti-Inflammatory Signaling and Phenotype of CD14+ Cells.

Lauri Polari, Anu Wiklund, Sofia Sousa, Lauri Kangas, Tero Linnanen, Pirkko Härkönen, Jorma Määttä

Open access · hybridAbstract read
In one paragraph

Article in Inflammation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
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.

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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. From Bone Health to Lifespan: Pleiotropic Effects of Antiresorptive Agents.Endocrinology and metabolism (Seoul, Korea) · 2025
    Review
  7. Review
  8. Inhibition of neuroinflammation and neuronal damage by the selective non-steroidal ERβ agonist AC-186.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. The Roles of Sex Hormones in the Course of Atopic Dermatitis.International journal of molecular sciences · 2019
    Review
  18. Novel Selective Estrogen Receptor Modulator Ameliorates Murine Colitis.International journal of molecular sciences · 2019
    Article
  19. Review
  20. Review
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

7 authors at 2 institutions in 2 countries.

Lauri PolariInstitute of Biomedicine, University of Turku, Turku, Finland. lauri.polari@utu.fi.ORCID http://orcid.org/0000-0002-0052-6489
Anu WiklundInstitute of Biomedicine, University of Turku, Turku, Finland.
Sofia SousaInstitute of Biomedicine, University of Turku, Turku, Finland.
Lauri KangasForendo Pharma Ltd., Turku, Finland.
Tero LinnanenForendo Pharma Ltd., Turku, Finland.
Pirkko HärkönenInstitute of Biomedicine, University of Turku, Turku, Finland.
Jorma MäättäInstitute of Biomedicine, University of Turku, Turku, Finland.
University of Turku · FIUniversité Claude Bernard Lyon 1 · FR

Funding

Tekes decision diary # 473/31/2015
6 · The paper itself

Abstract

Signaling via estrogen receptors (ER) is recognized as an essential part of the immune regulation, and ER-mediated signaling is involved in autoimmune reactions. Especially ERα activation in immune cells has been suggested to skew cytokine production toward Th2/M2-type mediators, which can have protective effect on inflammatory diseases and reduce Th1 and Th17 responses. These effects are caused by increased alternative activation of macrophages and changes in the activation of different T cell populations. In humans, hormonal status has been shown to have a major impact on several inflammatory diseases. Selective estrogen receptor modulators (SERMs) are ER ligands that regulate ER actions in a tissue-specific manner mostly lacking the adverse effects of steroid hormones. The impact of SERMs on the immune system is less studied, but it is suggested that certain SERMs may also produce immunoprotective effects. Here, we show that two novel SERMs and raloxifene affect immune cells by promoting M2 macrophage phenotype, alleviating NFκB activity, inhibiting T cell proliferation, and stimulating the production of anti-inflammatory compounds such as IL10 and IL1 receptor antagonist. Thus, these compounds have high potency as drug candidates against autoimmune diseases.

Indexed as

AdultCell LineCell Line, TumorCells, CulturedHumansInflammationLipopolysaccharide ReceptorsMacrophagesMiddle AgedNF-kappa BRaloxifene HydrochlorideSelective Estrogen Receptor ModulatorsSignal TransductionTh2 CellsYoung AdultLipopolysaccharide ReceptorsNF-kappa BRaloxifene HydrochlorideSelective Estrogen Receptor Modulatorsestradiolestrogen receptorinflammationmacrophagesraloxifeneSERM

Identifiers

PMID29574654
PMCPMC6061028
OpenAlexW2794044183

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.