RORγt+ Treg to Th17 ratios correlate with susceptibility to Giardia infection

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作者
Ivet A. Yordanova
Alba Cortés
Christian Klotz
Anja A. Kühl
Markus M. Heimesaat
Cinzia Cantacessi
Susanne Hartmann
Sebastian Rausch
机构
[1] Freie Universität Berlin,Institute of Immunology, Centre for Infection Medicine
[2] University of Cambridge,Department of Veterinary Medicine
[3] Unit 16 Mycotic and Parasitic Agents and Mycobacteria,iPATH.Berlin, Core Unit for Immunopathology for Experimental Models
[4] Department of Infectious Diseases,Institute of Microbiology
[5] Robert Koch-Institute,undefined
[6] Charité - University Medicine Berlin,undefined
[7] corporate member of Freie Universität Berlin,undefined
[8] Humboldt-Universität zu Berlin,undefined
[9] and Berlin Institute of Health,undefined
[10] Infectious Diseases and Immunology Charité - University Medicine Berlin,undefined
[11] corporate member of Freie Universität Berlin,undefined
[12] Humboldt-Universität zu Berlin,undefined
[13] and Berlin Institute of Health,undefined
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摘要
Infections with Giardia are among the most common causes of food and water-borne diarrheal disease worldwide. Here, we investigated Th17, Treg and IgA responses, and alterations in gut microbiota in two mouse lines with varying susceptibility to Giardia muris infection. Infected BALB/c mice shed significantly more cysts compared with C57BL/6 mice. Impaired control of infection in BALB/c mice was associated with lower Th17 activity and lower IgA levels compared with C57BL/6 mice. The limited metabolic activity, proliferation and cytokine production of Th17 cells in BALB/c mice was associated with higher proportions of intestinal Foxp3+RORγt+ regulatory T cells and BALB/c mice developed increased RORγt+ Treg:Th17 ratios in response to G. muris infection. Furthermore, G. muris colonization led to a significantly reduced evenness in the gut microbial communities of BALB/c mice. Our data indicate that differential susceptibility to Giardia infections may be related to RORγt+ Treg controlling Th17 activity and that changes in the microbiota composition upon Giardia infection partially depend on the host background.
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