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Regulatory T Cells Promote Myositis and Muscle Damage in Toxoplasma gondii Infection
- Source :
- The Journal of Immunology. 198:352-362
- Publication Year :
- 2017
- Publisher :
- The American Association of Immunologists, 2017.
-
Abstract
- The coordination of macrophage polarization is essential for the robust regenerative potential of skeletal muscle. Repair begins with a phase mediated by inflammatory monocytes (IM) and proinflammatory macrophages (M1), followed by polarization to a proregenerative macrophage (M2) phenotype. Recently, regulatory T cells (Tregs) were described as necessary for this M1 to M2 transition. We report that chronic infection with the protozoan parasite Toxoplasma gondii causes a nonresolving Th1 myositis with prolonged tissue damage associated with persistent M1 accumulation. Surprisingly, Treg ablation during chronic infection rescues macrophage homeostasis and skeletal muscle fiber regeneration, showing that Tregs can directly contribute to muscle damage. This study provides evidence that the tissue environment established by the parasite could lead to a paradoxical pathogenic role for Tregs. As such, these findings should be considered when tailoring therapies directed at Tregs in inflammatory settings.
- Subjects :
- 0301 basic medicine
Immunology
Macrophage polarization
Biology
Lymphocyte Activation
Real-Time Polymerase Chain Reaction
T-Lymphocytes, Regulatory
Article
Proinflammatory cytokine
Mice
03 medical and health sciences
0302 clinical medicine
medicine
Animals
Immunology and Allergy
Macrophage
Muscle, Skeletal
Macrophage homeostasis
Myositis
Macrophages
Toxoplasma gondii
Skeletal muscle
Cell Differentiation
Macrophage Activation
Flow Cytometry
medicine.disease
biology.organism_classification
Adoptive Transfer
Mice, Inbred C57BL
Chronic infection
030104 developmental biology
medicine.anatomical_structure
Female
Toxoplasmosis
030215 immunology
Subjects
Details
- ISSN :
- 15506606 and 00221767
- Volume :
- 198
- Database :
- OpenAIRE
- Journal :
- The Journal of Immunology
- Accession number :
- edsair.doi.dedup.....1eb4977d4f10782af219166a35a8ea52