Natural autoantibodies to the gonadotropin-releasing hormone receptor in polycystic ovarian syndrome

PLoS One. 2021 Apr 2;16(4):e0249639. doi: 10.1371/journal.pone.0249639. eCollection 2021.

Abstract

Context: Polycystic ovarian syndrome (PCOS) is a complex disease with different subtypes and unclear etiology. Among the frequent comorbidities are autoimmune diseases, suggesting that autoantibodies (aAb) may be involved in PCOS pathogenesis.

Objective: As the gonadal axis often is dysregulated, we tested the hypothesis that aAb to the gonadotropin-releasing hormone receptor (GnRH-R) are of diagnostic value in PCOS.

Design: An in vitro assay for quantifying aAb to the GnRH-R (GnRH-R-aAb) was established by using a recombinant fusion protein of full-length human GnRH-R and firefly luciferase. A commercial rabbit antiserum to human GnRH-R was used for standardization. Serum samples of control subjects and different cohorts of European PCOS patients (n = 1051) were analyzed.

Results: The novel GnRH-R-aAb assay was sensitive, and signals were linear on dilution when tested with the commercial GnRH-R antiserum. Natural GnRH-R-aAb were detected in one control (0.25%) and two PCOS samples (0.31%), and 12 samples were slightly above the threshold of positivity. The identification of samples with positive GnRH-R-aAb was reproducible and the signals showed no matrix interferences.

Conclusion: Natural GnRH-R-aAb are present in a very small fraction of adult control and PCOS subjects of European decent. Our results do not support the hypothesis that the GnRH-R constitutes a relevant autoantigen in PCOS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Autoantibodies / blood*
  • Autoantibodies / immunology
  • Biomarkers / blood*
  • Case-Control Studies
  • Female
  • Humans
  • Polycystic Ovary Syndrome / blood
  • Polycystic Ovary Syndrome / diagnosis*
  • Polycystic Ovary Syndrome / immunology
  • Receptors, LHRH / immunology*
  • Young Adult

Substances

  • Autoantibodies
  • Biomarkers
  • GNRHR protein, human
  • Receptors, LHRH

Grants and funding

The research has been funded by the Deutsche Forschungsgemeinschaft (DFG), Research Unit FOR- 2558 “TraceAge” (Scho 849/6-1), by the Austrian Research Promotion Agency FFG (FFG844609), the Center for Biomarker Research in Medicine (CBmed) in Graz, and we acknowledge financial support by the Open Access Publication Fund of Charité – Universitätsmedizin Berlin.