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Early hepatic cytokine mRNA expression in experimental rat fasciolosis
O Tliba1, P Sibille, C Boulard
1Laboratoire d'Immunopathologie des Maladies Parasitaires, Centre de Tours, Institut National de la Recherche Agronomique (INRA), Station de Pathologie Aviaire et de Parasitologie 37380 Nouzilly, France. tliba@tours.inra.fr
Abstract:
We studied the development of the cellular response, particularly with respect to Th1 and Th2 cytokine mRNA levels, in rat liver during the first 14 days of experimental infection with Fasciola hepatica. We analysed the panel of cytokines involved in initiation of the inflammatory and immune response. The levels of various mRNAs, particularly those primarily associated with the acute inflammatory response, and those commonly associated with T-cell proliferation and differentiation, were assessed by reverse transcription-polymerase chain reaction (RT-PCR) in liver samples. We also investigated the immune and inflammatory mediators balance in the liver, draining lymph node and spleen, by RT-competitive PCR quantification of mRNA levels for IL-4, IL-10 and IFN-gamma. Our data provide the first evidence that, in the early phase of infection, the inflammatory response in the liver of infected animals is transiently depressed or delayed. A Th0 profile was initially observed in the liver and hepatic lymph node, which developed into a Th2 profile 2 weeks after infection in the liver only. In the spleen, cytokine down-regulation was initiated and maintained during this period, suggesting that the parasite acts differently locally and in the periphery.
Insights
This study reveals that Fasciola hepatica infection initially delays the liver
Area of Science:
- Immunology
- Parasitology
- Molecular Biology
Background:
- Fasciola hepatica infection elicits complex immune responses.
- Understanding early cellular responses is crucial for host-parasite interactions.
Purpose of the Study:
- To investigate the early development of cellular immune responses in rat liver following Fasciola hepatica infection.
- To analyze cytokine mRNA profiles (Th1/Th2) and inflammatory mediators during the initial 14 days of infection.
Main Methods:
- Reverse transcription-polymerase chain reaction (RT-PCR) was used to quantify cytokine mRNA levels.
- Analysis included liver, draining lymph node, and spleen samples.
- Specific cytokines measured: IL-4, IL-10, and IFN-gamma.
Main Results:
- Early inflammatory response in the liver was transiently depressed or delayed.
- A Th0 cytokine profile was observed initially in the liver and hepatic lymph node.
- A Th2 profile developed in the liver by week 2, while the spleen showed sustained cytokine down-regulation.
Conclusions:
- Fasciola hepatica infection initially suppresses the hepatic inflammatory response.
- The parasite induces distinct local (liver) and peripheral (spleen) immune modulations.
- A shift towards a Th2-biased response occurs in the liver during early infection.