Sato Fumitaka, Omura Seiichi, Kawai Eiichiro, Martinez Nicholas E, Acharya Madan M, Reddy Pratap C, Chaitanya Ganta V, Alexander J Steven, Tsunoda Ikuo
Cell Immunol. 2014 Nov-Dec;292(1-2):85-93. doi: 10.1016/j.cellimm.2014.10.004.
We established a novel model of myocarditis induced with Theiler’s murine encephalomyelitis virus (TMEV), which has been used as a viral model for multiple sclerosis and seizure/epilepsy. Following TMEV infection, C3H mice developed severe myocarditis with T cell infiltration, while C57BL/6 mice had mild lesions and SJL/J mice had no inflammation in the heart. In C3H mice, myocarditis was divided into three phases: acute viral, subacute immune, and chronic fibrotic phases. Using toll-like receptor (TLR) 4-deficient C3H mice, we found that interleukin (IL)-6, IL-17, TLR4, and anti-viral immune responses were associated with myocarditis susceptibility.
我们建立了一种由泰勒氏鼠脑脊髓炎病毒(TMEV)诱导的心肌炎新模型,该病毒已被用作多发性硬化症和癫痫的病毒模型。TMEV感染后,C3H小鼠发生严重心肌炎并伴有T细胞浸润,而C57BL/6小鼠病变较轻,SJL/J小鼠心脏无炎症。在C3H小鼠中,心肌炎分为三个阶段:急性病毒期、亚急性免疫期和慢性纤维化期。使用 toll 样受体(TLR)4缺陷的C3H小鼠,我们发现白细胞介素(IL)-6、IL-17、TLR4和抗病毒免疫反应与心肌炎易感性有关。