Z Gastroenterol 2025; 63(08): e554
DOI: 10.1055/s-0045-1810982
Abstracts | DGVS/DGAV
Kurzvorträge
Prognoseparameter und Therapiekonzepte bei HCC Freitag, 19. September 2025, 09:51 – 11:11, Seminarraum 14 + 15

Schistosoma mansoni egg-derived antigens stimulate IGF1-receptor signaling in the liver and colon

Authors

  • S Wald

    1   Department of Gastroenterology, Justus Liebig University Giessen, 35392 Giessen, Germany, Gießen, Deutschland
  • V von Bülow

    1   Department of Gastroenterology, Justus Liebig University Giessen, 35392 Giessen, Germany, Gießen, Deutschland
  • F Stettler

    1   Department of Gastroenterology, Justus Liebig University Giessen, 35392 Giessen, Germany, Gießen, Deutschland
  • G Schramm

    2   Early Life Origin of Chronic Lung Diseases, Priority Research Area Chronic Lung Diseases, Research Center Borstel, Borstel, Deutschland
  • C G Grevelding

    3   Institute of Parasitology, BFS, Justus Liebig University, Gießen, Deutschland
  • M Roderfeld

    1   Department of Gastroenterology, Justus Liebig University Giessen, 35392 Giessen, Germany, Gießen, Deutschland
  • E Roeb

    1   Department of Gastroenterology, Justus Liebig University Giessen, 35392 Giessen, Germany, Gießen, Deutschland
 

Background: Schistosomiasis is a parasitic disease that affects more than 250 million individuals worldwide. Compelling evidence suggests that schistosome eggs, rather than adult worms, are responsible for significant tissue damage. S. mansoni eggs induce metabolic exhaustion and redox imbalance, which are critical for the integrity of hepatocellular DNA. However, the precise mechanism by which egg antigens transmit signals into host cells remains unclear. In this study, we investigated whether S. mansoni egg antigens regulate the metabolic pathways of hepatocytes and enterocytes through the insulin/insulin-like-growth-factor-receptor-1(IGF-1) receptor.

Methods: We employed RT-PCR array, western blotting, and immunohistochemistry to analyze markers of insulin/IGF-1 receptor signaling in liver and colon tissue of mice infected with S. mansoni. Additionally, we conducted functional experiments using colon epithelial cell lines, which involved western blotting and assessment of AP-1 promoter activity.

Results: S. mansoni infection in mice led to an upregulation of the following gene expression: Igf2, Dok, Aebp1, Leptin, and Akt3, with Serpine1 being the most strongly induced. Conversely, infection caused a decrease in the expression of Sos1, Irs1, and Gck, with G6pc being the most strongly downregulated gene. Additionally, the activation of the insulin/IGF-1 receptor was pronounced in the perigranulomatous hepatocytes. Mechanistic experiments utilizing the insulin/IGF-1 receptor inhibitor BMS 536924 revealed that S. mansoni egg antigens induced the activation of the insulin/IGF-1 receptor signaling cascade, including the activation of the proto-oncogene c-Jun.

Conclusions: Our findings demonstrate that S. mansoni soluble egg antigens modulate the insulin/IGF-1 receptor signaling pathway in both, murine and human hepatocytes and enterocytes, leading to an inhibition of gluconeogenesis. This suggests that the parasite's soluble egg antigens may enhance insulin sensitivity in the host. In a European cohort study serum IGF-1 correlates with the overall survival of patients with HCC. Thus IGF-1 might serve as a useful additional parameter for patient risk stratification. However, it remains unclear whether increased insulin signaling influences the prognosis during S. mansoni infection.



Publikationsverlauf

Artikel online veröffentlicht:
04. September 2025

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