Evidence map›Paper›PMID 24117194›Full record

ArticleAutoimmunity2014

DNA methylation modulates HRES1/p28 expression in B cells from patients with Lupus.

Tinhinane Fali, Christelle Le Dantec, Yosra Thabet, Sandrine Jousse, Catherine Hanrotel, Pierre Youinou, Wesley H Brooks, Andras Perl, Yves Renaudineau

Open access · greenAbstract read
In one paragraph

Article in Autoimmunity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 91 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Towards precision medicine for systemic lupus erythematosus and neuropsychiatric manifestations.Expert review of precision medicine and drug development · 2025
    Article
  5. Human Endogenous Retroviruses Expression in Autoimmunity.The Yale journal of biology and medicine · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. Lupus, DNA Methylation, and Air Pollution: A Malicious Triad.International journal of environmental research and public health · 2022
    Review
  10. Review
  11. Editorial: Epigenetic aspects of autoimmune diseases.Frontiers in cell and developmental biology · 2022
    Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. 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

9 authors at 4 institutions in 3 countries.

Tinhinane FaliEA2216 "Immunology, Pathology and Immunotherapy", University of Brittany, SFR ScinBios and Labex Igo "Immunotherapy Graft, Oncology" , Brest , France .
Christelle Le Dantec
Yosra Thabet
Sandrine Jousse
Catherine Hanrotel
Pierre Youinou
Wesley H Brooks
Andras Perl
Yves Renaudineau
Centre Hospitalier Régional Universitaire de Brest · FRBipar · FRSyracuse University · USUniversité de Bretagne Occidentale · FR

Funding

Metabolic Control of T-cell Lineage Specification in SLER01AI072648 · NIAID · UPSTATE MEDICAL UNIVERSITY · PI PERL, ANDRAS · 2008 to 2024
$6.1M
IMPACT OF HRES-1 ENDOGENOUS RETROVIRUS IN SLER01AI048079 · NIAID · UPSTATE MEDICAL UNIVERSITY · PI PERL, ANDRAS · 2000 to 2013
$2.7M
Genetic and Immunological Impact of the HRES-1/Rab4 Locus in SLER56AI048079 · NIAID · UPSTATE MEDICAL UNIVERSITY · PI PERL, ANDRAS · 2008 to 2008
$275k
NIAID NIH HHS AI048079NIAID NIH HHS AI072648NIAID NIH HHS R01 AI048079NIAID NIH HHS R01 AI072648NIAID NIH HHS R56 AI048079
6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) disease is an autoimmune disease of unknown aetiology that affects predominantly women of child bearing age. Since previous studies, including ours, have demonstrated that CD4+ T cells and B cells from SLE patients are defective in their ability to methylate their DNA upon antigen stimulation, the aim of this study was to investigate whether DNA demethylation affects the transcription of HRES-1 in B cells. HRES-1 is the prototype of Human Endogenous Retrovirus (HERV) overexpressed in SLE. We have observed that SLE B cells were characterized by their incapacity to methylate the HRES-1 promoter, both in unstimulated and in anti-IgM stimulated B cells. In turn, HRES-1/p28 expression was increased in SLE B cells after B cell receptor engagement, but not in controls. In SLE B cells the Erk/DNMT1 pathway was defective. In addition, blocking the autocrine-loop of IL-6 in SLE B cells with an anti-IL-6 receptor monoclonal antibody restores DNA methylation and control of HRES-1/p28 expression became effective. As a consequence, a better understanding of HERV dysregulation in SLE reinforces our comprehension of the disease and opens new therapeutic perspectives.

Indexed as

AdultAntigens, NuclearAutoantigensB-LymphocytesDNA MethylationGene Expression RegulationHumansInterleukin-6Lupus Erythematosus, SystemicMiddle AgedReceptors, Interleukin-6Retroviridae ProteinsAntigens, NuclearAutoantigensHRES-1 p28 protein, human retroviral elementInterleukin-6Receptors, Interleukin-6Retroviridae ProteinsB cellsDNA methylationErkHRES-1IL-6systemic lupus erythematosus

Identifiers

PMID24117194
PMCPMC4034120
OpenAlexW1989970595

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.