Publications by authors named "Laura Hehr"

Article Synopsis
  • Schistosomiasis, a parasitic infection affecting over 200 million people, primarily causes liver-related morbidity through its eggs rather than adult worms.
  • Research methods involved advanced imaging and biochemical techniques on hamster models and human cell lines, validating findings with human biopsies.
  • The study found that the infection leads to lipid and glycogen depletion in the liver, with parasites reprogramming host metabolism, resulting in oxidative stress and DNA damage, indicating a severe impact on liver cells regardless of the immune response.
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Protein kinases have been discussed as promising druggable targets in various parasitic helminths. New drugs are also needed for control of fascioliasis, a food-borne trematode infection and worldwide spread zoonosis, caused by the liver fluke and related species. In this study, we intended to move protein kinases more into the spotlight of drug research and characterized the fasciolicidal activity of two small-molecule inhibitors from human cancer research: the Abelson tyrosine kinase (ABL-TK) inhibitor imatinib and the polo-like 1 (PLK1) inhibitor BI2536.

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Schistosomiasis (bilharzia) is a neglected tropical disease caused by parasitic flatworms of the genus Schistosoma, with considerable morbidity in parts of the Middle East, South America, Southeast Asia, in sub-Saharan Africa, and particularly also in Europe. The WHO describes an increasing global health burden with more than 290 million people threatened by the disease and a potential to spread into regions with temperate climates like Corsica, France. The aim of our study was to investigate the influence of S.

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Clinical studies demonstrated that nonalcoholic steatohepatitis is associated with liver-related outcomes in chronic hepatitis B. Furthermore, primary biliary fibrosis and biliary atresia occurred in patients with HBV infection. Interestingly, hepatitis B virus surface protein (HBs) transgenic mice spontaneously develop hepatic steatosis.

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