Evidence map›Paper›PMID 41760363›Full record

ArticleACR open rheumatology2026

Anti-CD146 Autoantibodies: The First Biologic Markers Associated With Occupational Exposure in Systemic Sclerosis.

Julien Bermudez, Xavier Heim, Elise Kaspi, Charlotte Reytier, Abdelouahab Beziane, Robin Arcani, Audrey Benyamine, Brigitte Granel, Antoine Villa, Marcel Blot-Chabaud and 5 more

Abstract read
In one paragraph

Article in ACR open rheumatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Julien BermudezAix Marseille Univ, APHM, INSERM, INRAE, C2VN, Hôpital Nord, Department of Respiratory Medicine, Marseille, France.ORCID https://orcid.org/0000-0001-8823-0959
Xavier HeimAix Marseille Univ, APHM, INSERM, INRAE, C2VN, Hôpital de la Timone, Biogénopôle, Laboratoire d'immunologie, Marseille, France.
Elise KaspiCell Biology Department, Aix Marseille University, APHM, INSERM, Marseille Medical Genetics, Timone Hospital, Marseille, France.
Charlotte ReytierAix Marseille Univ, APHM, INSERM, INRAE, C2VN, Hôpital de la Timone, Biogénopôle, Laboratoire d'immunologie, Marseille, France.
Abdelouahab BezianeAPHM, Hôpital de la Timone, Biogénopôle, Laboratoire d'immunologie, Marseille, France.
Robin ArcaniInternal Medicine and Therapeutics Department, Centre Hospitalier Universitaire (CHU) de la Timone, APHM, Marseille, France.ORCID https://orcid.org/0000-0002-5567-354X
Audrey BenyamineAix Marseille Univ, APHM, INSERM, INRAE, C2VN, Hôpital Nord, Department of Internal Medicine, Marseille, France.ORCID https://orcid.org/0000-0003-4187-3425
Brigitte GranelAix Marseille Univ, APHM, INSERM, INRAE, C2VN, Hôpital Nord, Department of Internal Medicine, Marseille, France.
Antoine VillaAix Marseille Univ, APHM, CEReSS, Timone Hospital, Department of Occupational Diseases, Marseille, France.
Marcel Blot-ChabaudAix Marseille University, APHM, INSERM, INRAE, C2VN, Marseille, France.ORCID https://orcid.org/0000-0003-0152-3893
Erwan DumontetCHU de Rennes, Pôle Biologie, Rennes, France.
Christophe ParisUniversity of Rennes, CHU Rennes, INSERM, École des Hautes études en Santé Publique (EHESP), Institut de recherche en santé, environnement et travail (Irset), UMR_S 1085, Rennes, France.
Alain LescoatUniversity of Rennes, CHU Rennes, INSERM, École des Hautes études en Santé Publique (EHESP), Institut de recherche en santé, environnement et travail (Irset), UMR_S 1085, Rennes, France.
Valérie LecureurUniversity of Rennes, CHU Rennes, INSERM, École des Hautes études en Santé Publique (EHESP), Institut de recherche en santé, environnement et travail (Irset), UMR_S 1085, Rennes, France.
Nathalie BardinAix Marseille Univ, APHM, INSERM, INRAE, C2VN, Hôpital de la Timone, Biogénopôle, Laboratoire d'immunologie, Marseille, France.

Funding

Agence Nationale de Sécurité Sanitaire de l'Alimentation, de l'Environnement et du TravailGroupe Francophone de Recherche sur la Sclérodermie
6 · The paper itself

Abstract

objectiveSystemic sclerosis (SSc) is a severe autoimmune disease, with occupational exposure being a significant risk factor. Because CD146 was recently identified as a driver of fibrosis in SSc through regulation of the Wnt/reactive oxygen species interplay, we hypothesized that it is a major autoimmune target in this disease.

methodsWe developed an in-house ELISA test to detect anti-CD146 autoantibodies (AACD146), which was confirmed by immunoprecipitation and Western blotting. AACD146 positivity was assessed in the sera of patients with SSc compared with healthy controls. A validation cohort of workers exposed to asbestos or silica was evaluated and compared to patients with pulmonary cancer and healthy controls without any occupational exposure.

resultsDetection of AACD146 was assessed by ELISA and confirmed with Western blot and an absorption test. In the first cohort, the prevalence of positive AACD146 was significantly higher in patients with SSc (n = 14 of 93; 15%) than in controls (n = 2 of 40; 5%). Interestingly, among patients with SSc, positive AACD146 were associated with male sex (P = 0.04) and occupational exposure to silica (P = 0.009), with a sensitivity of 57% and specificity of 88% for occupational exposure. Results were confirmed in a validation cohort, in which positive AACD146 were found in 57% (n = 13 of 23) of patients with professional exposure. The frequency of AACD146 was significantly higher compared to controls (P = 0.03) and to patients with a history of cancer (P = 0.02).

conclusionWe demonstrated that AACD146 are detectable in patients with SSc and are linked to male workers with occupational dust exposure. AACD146 are the first biomarkers associated with occupational exposure in SSc, with potential implications for preventive medicine.

Identifiers

PMID41760363
PMCPMC12948552

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