Evidence map›Paper›PMID 29850618›Full record

ArticleJournal of immunology research2018

Conventional DCs from Male and Female Lupus-Prone B6.NZM Sle1/Sle2/Sle3 Mice Express an IFN Signature and Have a Higher Immunometabolism That Are Enhanced by Estrogen.

Michael H Lee, Marita Chakhtoura, Uma Sriram, Roberto Caricchio, Stefania Gallucci

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Immunometabolism in systemic lupus erythematosus.Nature reviews. Rheumatology · 2025
    Review
  2. Role of Sex Hormones in Prevalent Kidney Diseases.International journal of molecular sciences · 2023
    Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. FcγRIIb on CD11cAtherosclerosis · 2019
    Article
  8. 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 1 institution in 1 country.

Michael H LeeDepartment of Microbiology and Immunology, Lab of Dendritic Cell Biology, Lewis Katz School of Medicine, Temple University, Philadelphia, PA 19140, USA.
Marita ChakhtouraDepartment of Microbiology and Immunology, Lab of Dendritic Cell Biology, Lewis Katz School of Medicine, Temple University, Philadelphia, PA 19140, USA.
Uma SriramDepartment of Microbiology and Immunology, Lab of Dendritic Cell Biology, Lewis Katz School of Medicine, Temple University, Philadelphia, PA 19140, USA.
Roberto CaricchioDepartment of Medicine, Division of Rheumatology, Lewis Katz School of Medicine, Temple University, Philadelphia, PA 19140, USA.
Stefania GallucciDepartment of Microbiology and Immunology, Lab of Dendritic Cell Biology, Lewis Katz School of Medicine, Temple University, Philadelphia, PA 19140, USA.ORCID 0000-0003-4737-8003
Temple University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type I interferons (IFN) are pathogenic in systemic lupus erythematosus (SLE) and were proposed to control the immunometabolism of dendritic cells (DCs). We previously reported that DCs from female lupus-prone mice constitutively overexpress IFN-responsive genes resembling the IFN signature found in SLE patients. As SLE has higher incidence in women than men, more so in women of reproductive age, estrogens are suggested to affect lupus pathogenesis. We investigated the effects of sex and estrogens on the IFN signature in conventional GM-CSF-bone marrow-derived DCs (cDCs), from male and female Triple Congenic B6.NZM.

Indexed as

AnimalsAutoantibodiesBone Marrow CellsDendritic CellsDisease Models, AnimalEstradiolFemaleGranulocyte-Macrophage Colony-Stimulating FactorHumansInterferon Type ILupus Erythematosus, SystemicLupus NephritisLymphocyte ActivationMaleMiceMice, Inbred C57BLAutoantibodiesEstradiolGranulocyte-Macrophage Colony-Stimulating FactorInterferon Type I

Identifiers

PMID29850618
PMCPMC5925037
OpenAlexW2800039673

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.