Innate Signaling Promotes Formation of Regulatory Nitric Oxide-Producing Dendritic Cells Limiting T-Cell Expansion in Experimental Autoimmune Myocarditis

Article

关键词: COXSACKIEVIRUS B3 MYOCARDITIS;    TRYPANOSOMA-CRUZI INFECTION;    BACTERIAL-INFECTION;    GAMMA;    HEART;    MICE;    SYNTHASE;    INDUCTION;    RECEPTOR;    DISEASE;   

DOI  :  10.1161/CIRCULATIONAHA.112.000434

来源: SCIE

【 摘 要 】

Background- Activation of innate pattern-recognition receptors promotes CD4(+) T-cell-mediated autoimmune myocarditis and subsequent inflammatory cardiomyopathy. Mechanisms that counterregulate exaggerated heart-specific autoimmunity are poorly understood. Methods and Results- Experimental autoimmune myocarditis was induced in BALB/c mice by immunization with alpha-myosin heavy chain peptide and complete Freund's adjuvant. Together with interferon-gamma, heat-killed Mycobacterium tuberculosis, an essential component of complete Freund's adjuvant, converted CD11b(hi)CD11c(-) monocytes into tumor necrosis factor-alpha- and nitric oxide synthase 2-producing dendritic cells (TipDCs). Heat-killed M. tuberculosis stimulated production of nitric oxide synthase 2 via Toll-like receptor 2-mediated nuclear factor-kappa B activation. TipDCs limited antigen-specific T-cell expansion through nitric oxide synthase 2-dependent nitric oxide production. Moreover, they promoted nitric oxide synthase 2 production in hematopoietic and stromal cells in a paracrine manner. Consequently, nitric oxide synthase 2 production by both radiosensitive hematopoietic and radioresistant stromal cells prevented exacerbation of autoimmune myocarditis in vivo. Conclusions- Innate Toll-like receptor 2 stimulation promotes formation of regulatory TipDCs, which confine autoreactive T-cell responses in experimental autoimmune myocarditis via nitric oxide. Therefore, activation of innate pattern-recognition receptors is critical not only for disease induction but also for counterregulatory mechanisms, protecting the heart from exaggerated autoimmunity.

【 授权许可】

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