| Literature DB >> 27729270 |
Thiago Almeida Pereira1, Wing-Kin Syn2, Fausto E L Pereira3, José Roberto Lambertucci4, William Evan Secor5, Anna Mae Diehl6.
Abstract
Schistosomiasis is a major cause of fibrosis and portal hypertension. The reason 4-10% of infected subjects develops hepatosplenic schistosomiasis remains unclear. Chronically infected male CBA/J mice reproduce the dichotomic forms of human schistosomiasis. Most mice (80%) develop moderate splenomegaly syndrome (similar to hepatointestinal disease in humans) and 20% present severe hypersplenomegaly syndrome (analogous to human hepatosplenic disease). We demonstrated that the profibrogenic molecule osteopontin discriminates between mice with severe and mild disease and could be a novel morbidity biomarker in murine and human schistosomiasis. Failure to downregulate osteopontin during the chronic phase may explain why hepatosplenic subjects develop severe fibrosis. Copyright ÂEntities:
Keywords: Biomarker; Liver fibrosis; Osteopontin; Portal hypertension; Schistosomiasis mansoni
Mesh:
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Year: 2016 PMID: 27729270 PMCID: PMC5584370 DOI: 10.1016/j.ijpara.2016.08.004
Source DB: PubMed Journal: Int J Parasitol ISSN: 0020-7519 Impact factor: 3.981