Department of Microbiology and Immunology and Interdepartmental Immunobiology Center, Northwestern University Feinberg School of Medicine, 303, E. Chicago Ave., Chicago, IL 60611, USA.
Virology. 2010 Jun 20;402(1):102-11. doi: 10.1016/j.virol.2010.02.031. Epub 2010 Apr 8.
Theiler's murine encephalomyelitis virus (TMEV)-induced demyelinating disease (TMEV-IDD) is a relevant mouse model of multiple sclerosis. Infection of susceptible SJL/J mice leads to life-long CNS virus persistence and development of a chronic T cell-mediated autoimmune demyelinating disease triggered via epitope spreading to endogenous myelin epitopes. Potent CNS-infiltrating CD8(+) T cell responses to TMEV epitopes have previously been shown to be induced in both disease-susceptible SJL/J and resistant C57BL/6 mice, in which the virus is rapidly cleared. Specific tolerization of SJL CD8(+) T cells specific for the immunodominant TMEV VP3(159)(-)(166) epitope has no effect on viral load or development of clinical TMEV-IDD, but adoptive transfer of activated CD8(+) VP3(159)(-)(166)-specific T cell blasts shortly after TMEV infection to boost the early anti-viral response leads to clearance of CNS virus and protection from subsequent TMEV-IDD. These studies have important implications for vaccine strategies and treatment of chronic infections in humans.
Theiler 氏鼠脑脊髓炎病毒(TMEV)诱导的脱髓鞘疾病(TMEV-IDD)是多发性硬化症的一种相关的小鼠模型。易感 SJL/J 小鼠感染后会导致中枢神经系统病毒持续存在,并发展为慢性 T 细胞介导的自身免疫性脱髓鞘疾病,这是通过抗原表位扩展到内源性髓鞘抗原引发的。先前已经表明,在易感的 SJL/J 和抗性 C57BL/6 小鼠中均可诱导针对 TMEV 表位的强效中枢神经系统浸润 CD8(+) T 细胞反应,而在这些小鼠中,病毒会迅速清除。特异性耐受 SJL CD8(+) T 细胞针对免疫优势 TMEV VP3(159)(-)(166)表位的反应对病毒载量或临床 TMEV-IDD 的发展没有影响,但在 TMEV 感染后不久过继转移激活的 CD8(+) VP3(159)(-)(166)-特异性 T 细胞母细胞以增强早期抗病毒反应可导致中枢神经系统病毒清除,并防止随后发生 TMEV-IDD。这些研究对人类慢性感染的疫苗策略和治疗具有重要意义。