Regulatory T Cells Promote Myositis and Muscle Damage in Toxoplasma gondii Infection

被引:35
作者
Jin, Richard M. [1 ]
Blair, Sarah J. [1 ]
Warunek, Jordan [1 ]
Heffner, Reid R. [2 ]
Blader, Ira J. [1 ]
Wohlfert, Elizabeth A. [1 ]
机构
[1] SUNY Buffalo, Univ Buffalo, Jacobs Sch Med & Biomed Sci, Dept Microbiol & Immunol, Buffalo, NY 14214 USA
[2] SUNY Buffalo, Univ Buffalo, Jacobs Sch Med & Biomed Sci, Dept Pathol & Anat Sci, Buffalo, NY 14214 USA
基金
美国国家卫生研究院;
关键词
IFN-GAMMA PRODUCTION; SKELETAL-MUSCLE; MACROPHAGE PHENOTYPE; MONOCYTES; DIFFERENTIATION; INFLAMMATION; MICE; REGENERATION; IMMUNITY; DERMATOMYOSITIS;
D O I
10.4049/jimmunol.1600914
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:352 / 362
页数:11
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