Evidence map›Paper›PMID 40417978›Full record

ReviewEuropean journal of immunology2025

The Inactive X Chromosome: A Genetic Driver of Female-Biased Rheumatic Autoimmune Disorders?

Léa Ferrayé, Mélissa Nieucel, Magali Savignac, Julie Chaumeil, Jean-Charles Guéry

Abstract readReview
In one paragraph

Review in European journal of immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. The SLC15A4-TASL complex is essential for lupus development in mice.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
  4. 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

5 authors.

Léa FerrayéToulouse Institute for Infectious and Inflammatory Diseases (INFINITY), Université de Toulouse, INSERM, CNRS, Toulouse, France.
Mélissa NieucelToulouse Institute for Infectious and Inflammatory Diseases (INFINITY), Université de Toulouse, INSERM, CNRS, Toulouse, France.
Magali SavignacToulouse Institute for Infectious and Inflammatory Diseases (INFINITY), Université de Toulouse, INSERM, CNRS, Toulouse, France.
Julie ChaumeilInstitut Cochin, Université Paris Cité, CNRS, INSERM, Paris, France.
Jean-Charles GuéryToulouse Institute for Infectious and Inflammatory Diseases (INFINITY), Université de Toulouse, INSERM, CNRS, Toulouse, France.ORCID 0000-0003-4499-3270

Funding

Agence Nationale de la Recherche ANR-20-CE15-0014-01Agence Nationale de la Recherche ANR-23-CE15-0002-01Fondation pour la Recherche Médicale EQU202403018065FOREUM Foundation 2020-041Novartis DREAMER 2023Région Occitanie/Pyrénées-Méditerranée 1901175
6 · The paper itself

Abstract

Females have a better ability to resolve infections compared to males, but also a greater susceptibility to develop autoimmunity. Besides the initial interest in the contribution of sex-steroid hormone signaling, the role of genetic factors linked to the X chromosome has recently received much attention. In humans and mice, the number of X chromosomes, rather than sex-steroid hormones, is associated with a higher risk to develop autoimmunity, particularly rheumatic diseases, such as SLE, Sjögren's syndrome, or systemic sclerosis. In this review, we will summarize the recent advances in the various mechanisms and pathways involving the X chromosome in female sex-biased autoimmune diseases. We will particularly focus on the experimental evidence suggesting that expression of X-linked genes due to dysregulation in X chromosome inactivation maintenance could contribute to the female predisposition for autoautoimmunity.

Indexed as

Autoimmune DiseasesChromosomes, Human, XRheumatic DiseasesX Chromosome InactivationAnimalsAutoimmunityFemaleGenetic Predisposition to DiseaseHumansMaleMiceautoimmune diseasessex biassystemic lupus erythematosusX chromosome inactivation

Identifiers

PMID40417978
PMCPMC12105428

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.