Elevated interleukin-33, CD1c+ dendritic cells, and interleukin-17A in peritoneal fluid of patients with endometriosis: a case-control study

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This case-control study found that peritoneal fluid from endometriosis patients exhibits elevated interleukin-33, interleukin-17A, and activated CD1c+ dendritic cells, suggesting these factors drive disease pathogenesis through IL-33-induced DC maturation.

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Abstract

BACKGROUND: Endometriosis (EMS) is a chronic inflammatory disorder involving ectopic endometrial tissue growth. This study investigated IL-33, CD1c+ dendritic cells (DCs) and their co-stimulatory molecules (CD40, CD80, CD86), and IL-17 A in the peritoneal fluid (PF) of EMS patients, and explored their interrelationships. METHODS AND RESULTS: PF samples were obtained from 42 women with EMS as experimental subjects and 31 women without EMS as controls. Enzyme-linked immunosorbent assay (ELISA) showed that PF IL-33 (P < 0.001) and IL-17 A (P < 0.01) levels were significantly elevated in EMS patients vs. controls. Moreover, IL-33 levels were significantly higher in stages III-IV than I-II (P  0.05). However, the proportions of CD1c+CD40+ (P < 0.001), CD1c+CD80+ (P < 0.05), and CD1c+CD86+ (P < 0.01) DCs were significantly elevated in EMS, with CD1c+CD40 + higher in stages III-IV vs. I-II (P < 0.05). For in vitro experiments, control PF mononuclear cells (PFMCs) were incubated with recombinant IL-33 (100 ng/mL) for 24 h. IL-33 treatment increased IL-17 A production and CD1c+CD40 + and CD1c+CD80 + DC frequences in control PFMCs compared to unstimulated PFMCs (all P < 0.05). CONCLUSION: Elevated IL-33 and IL-17 A levels, along with enhanced CD1c + DC maturation and activation in PF, may contribute to EMS pathogenesis and progression. IL-33 may promote disease development by inducing CD1c + DC maturation/activation, thus increasing IL-17 A production.

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MeSH descriptors

Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1 Antigens, CD1

Citation neighborhood

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. [ expand to 2 hops ] — adds papers reached through this work's immediate citers/citees. Heavier; up to 60 extra dots.

References (50)

SciLite annotations

organisms 3
noordeloos 2009062 noordeloos 2009062 talaromyces euchlorocarpius

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