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Trichuris muris Infection: A Model of Type 2 Immunity and Inflammation in the Gut
Published on: May 24, 2011
In vitro antigen presenting cell-derived IL-10 and IL-6 correlate with Trichuris muris isolate-specific survival
Parasite Immunology
|February 19, 2009
Summary
The whipworm (Trichuris muris) S isolate, unlike E and J isolates, persists in mice. This persistence may be due to unique antigens that promote IL-10 and IL-6 production by immune cells, hindering protective responses.
Area of Science:
- Immunology
- Parasitology
- Molecular Biology
Background:
- Trichuris muris is a model for human whipworm infections.
- The S isolate of T. muris persists in C57BL/6 mice, while E and J isolates are cleared.
- S isolate persistence is linked to unique excretory/secretory (E/S) antigens that may suppress T cell responses.
Purpose of the Study:
- To investigate differential immune responses of antigen-presenting cells (APCs) to E/S antigens from T. muris isolates.
- To determine if E/S antigens from the S isolate induce distinct cytokine profiles in macrophages and dendritic cells.
Main Methods:
- Bone marrow-derived macrophages (BMMPhi) and dendritic cells (BMDCs) were cultured in vitro.
- Cells were stimulated with isolate-specific E/S antigens.
- Flow cytometry (FACS) was used to analyze co-stimulation markers and MHC-II levels.
- Cytokine levels (IL-10, IL-6) in supernatants were quantified.
Main Results:
- S isolate E/S antigens induced significantly higher levels of IL-10 and IL-6 from both BMMPhi and BMDCs compared to E and J isolates.
- No significant differences were observed in co-stimulation markers or MHC-II levels across isolates.
Conclusions:
- In vitro data suggest that T. muris S isolate E/S antigens promote a regulatory cytokine environment via increased IL-10 and IL-6 production.
- This immune modulation by S isolate antigens may contribute to its in vivo persistence by suppressing effective anti-parasitic immune responses.

