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Intraperitoneal Echinococcus multilocularis infection in mice modulates peritoneal CD4+ and CD8+ regulatory T cell
Naceur Mejri1, Norbert Müller, Andrew Hemphill
1Institute of Parasitology, University of Bern, Bern, Switzerland.
Echinococcus multilocularis infection in mice promotes regulatory T cells (Treg), leading to an impaired immune response and increased parasite survival. This study identifies specific T cell populations and dendritic cell dysfunction contributing to immune evasion in chronic infection.
Area of Science:
- Immunology
- Parasitology
- Cell Biology
Background:
- Echinococcus multilocularis infection leads to impaired host immunity, favoring parasite survival.
- Chronic infection is characterized by an altered peritoneal immune cell profile.
Purpose of the Study:
- To investigate the immune response in the peritoneal cavity during chronic Echinococcus multilocularis infection.
- To characterize the role of T cells and dendritic cells in host immune evasion.
Main Methods:
- Flow cytometry to analyze CD4+ and CD8+ peritoneal T (pT) cells.
- Quantitative PCR to assess cytokine mRNA expression (IL-4, IFN-γ, TGF-β, IL-10, IL-12).
- Analysis of dendritic cell (DC) surface marker expression and co-culture experiments to evaluate T cell proliferation.
Main Results:
- Infected mice showed increased CD4+ and CD8+ pT cells with a Th2-biased response (high IL-4, low IFN-γ).
- Peritoneal dendritic cells (AE-pDCs) exhibited suppressed maturation markers and reduced ability to stimulate T cell proliferation.
- Regulatory T cells (Treg), including CD4+CD25+ and Foxp3+ subpopulations, were identified and shown to inhibit T cell proliferation.
Conclusions:
- Echinococcus multilocularis infection induces a Th2-skewed immune response and functional impairment of peritoneal dendritic cells.
- Regulatory T cells play a significant role in modulating the host immune response, contributing to parasite persistence.
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