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Published on: May 18, 2016
Cellular responses during liver fluke infection in sheep and its evasion by the parasite
E Meeusen1, C S Lee, M D Rickard
1Centre for Animal Biotechnology, University of Melbourne, Parkville, Victoria, Australia.
Insights
Sheep immune responses to liver fluke infections involve distinct cellular changes in the liver and lymph nodes. Secondary infections show a heightened immune cell infiltration and parasite evasion.
Area of Science:
- Immunology
- Parasitology
- Veterinary Medicine
Background:
- Liver fluke infections pose significant challenges in livestock.
- Understanding the host immune response is crucial for developing effective control strategies.
Purpose of the Study:
- To investigate the cellular immune response in sheep during primary and secondary liver fluke infections.
- To analyze immune cell populations in liver tissue and draining lymph nodes.
Main Methods:
- Immunohistology of liver tissue.
- Flow cytometry of lymphocytes from hepatic lymph nodes.
- Comparison of acute/chronic primary and acute secondary infections.
Main Results:
- Primary infection: CD4+, CD8+ T cells infiltrate portal tracts; young flukes present.
- Secondary infection: Increased eosinophils, B cells, CD4+ T cells; MHC class II+ cells; no young flukes.
- Chronic infection: Fibrosis, CD8+, gamma delta-TCR+ T cells, B cell follicles; egg-induced inflammation.
Conclusions:
- Sheep mount distinct cellular immune responses to different stages of liver fluke infection.
- Parasite evasion mechanisms are evident, particularly during secondary infections.
- Lymph node changes reflect the systemic immune response to infection.
Abstract:
The cellular immune response in sheep to an acute and chronic primary and an acute secondary liver fluke infection were examined by immunohistology of liver tissue and flowcytometry of lymphocytes from the draining hepatic lymph nodes. Ten days after primary infection, portal tract areas surrounding migratory tunnels were infiltrated with CD4+ and CD8+ lymphocytes with fewer B cells and T19+ T cells. Micro abscesses were distributed sporadically in the liver parenchyma and young flukes could be easily observed in the liver tissue free from inflammatory cells. More intensive infiltration of the portal tract areas was observed during a secondary liver fluke infection characterized by a pronounced increase in eosinophils, B cells and CD4+ T cells. In addition, there was an increase in MHC class II+ fibroblastic-like cells surrounding the migratory tracts. In contrast to the primary infection, no young flukes were observed in the same tissue areas during the secondary infection. Chronic primary infections were characterized by perilobular fibrosis and a predominance of CD8+ and gamma delta-TCR+T19- T cells distributed within fibrotic strands. Distinct B cell follicles were observed in the fibrotic strands and near major bile ducts and necrotic patches. Pronounced lymphocyte infiltration could occasionally be observed surrounding liver fluke eggs lodged in liver tissue. A progressive increase in lymph node weight, cell number and CD4/CD8 ratio was observed in the acute and chronic primary infections. The role of the infiltrating cell populations and possible mechanism of immune evasion by the parasite are discussed.
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