High Levels of Anti-GM-CSF Antibodies in Deep Infiltrating Endometriosis.


Journal

Reproductive sciences (Thousand Oaks, Calif.)
ISSN: 1933-7205
Titre abrégé: Reprod Sci
Pays: United States
ID NLM: 101291249

Informations de publication

Date de publication:
01 2020
Historique:
received: 04 02 2019
accepted: 25 03 2019
pubmed: 13 2 2020
medline: 15 12 2020
entrez: 13 2 2020
Statut: ppublish

Résumé

Endometriosis is a chronic hormono-dependent inflammatory gynecological disease. Endometriosis can be subdivided into three forms: superficial peritoneal implants, endometrioma, and deep infiltrating endometriosis (DIE). Inflammation is a typical feature of endometriosis with overproduction of prostaglandins, chemokines, and cytokines, like granulocyte-macrophage colony-stimulating factor (GM-CSF). GM-CSF is a hematopoietic growth factor and immune modulator which belongs to the group of cytokines that actively participate in inflammatory reactions. GM-CSF autoantibodies (Ab) are described in inflammatory diseases such as Crohn disease and ulcerative colitis where high concentrations of anti-GM-CSF Ab are correlated with severity, complications, and relapses. We have evaluated the presence of anti-GM-CSF Ab in the serum of 106 patients with endometriosis and 92 controls using a home-made enzyme-linked immunosorbent assay (ELISA) and correlated the results with the form and severity of the disease. We found that anti-GM-CSF Ab level is significantly increased in the sera of patients with endometriosis compared to controls and is associated with the severity of the disease especially in patients with deep endometriosis (p < 0.0001) with the highest number of lesions (p = 0.0034), including digestive involvement (p = 0.0041). We also found a correlation between these levels of anti-GM-CSF Ab and the number of lesions in DIE patients (r = 0.913). In this way, searching anti-GM-CSF Ab in endometriosis patient sera could be of value for patient follow-up and put further insight into the role of inflammation and of GM-CSF in endometriosis pathogenesis.

Identifiants

pubmed: 32046390
doi: 10.1007/s43032-019-00021-8
pii: 10.1007/s43032-019-00021-8
doi:

Substances chimiques

Autoantibodies 0
Granulocyte-Macrophage Colony-Stimulating Factor 83869-56-1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

211-217

Auteurs

Laurie Toullec (L)

Department of Immunology, Cochin University Hospital, APHP, Paris, France.
Department of Immuno-hematology, Henri Mondor University Hospital, APHP, Créteil, France.

Frédéric Batteux (F)

Department of Immunology, Cochin University Hospital, APHP, Paris, France. frederic.batteux@aphp.fr.
INSERM U1016, Institut Cochin, Paris, France. frederic.batteux@aphp.fr.

Pietro Santulli (P)

Department of Gynecology Obstetrics II and Reproductive Medicine, Cochin University Hospital, Paris, France.
INSERM U1016, Institut Cochin, Paris, France.

Sandrine Chouzenoux (S)

INSERM U1016, Institut Cochin, Paris, France.

Mohamed Jeljeli (M)

Department of Immunology, Cochin University Hospital, APHP, Paris, France.
INSERM U1016, Institut Cochin, Paris, France.

Thibaut Belmondo (T)

Department of Immuno-hematology, Henri Mondor University Hospital, APHP, Créteil, France.

Sophie Hue (S)

Department of Immuno-hematology, Henri Mondor University Hospital, APHP, Créteil, France. sophie.hue@aphp.fr.

Charles Chapron (C)

Department of Gynecology Obstetrics II and Reproductive Medicine, Cochin University Hospital, Paris, France. charles.chapron@aphp.fr.
INSERM U1016, Institut Cochin, Paris, France. charles.chapron@aphp.fr.

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