Escriou N, Leclerc C, Gerbard S, Giraud M, van der Werf S
Unité de Virologie Moléculaire, URA CNRS#1966, Institut Pasteur, Paris, France.
J Gen Virol. 1995 Aug;76 ( Pt 8):1999-2007. doi: 10.1099/0022-1317-76-8-1999.
The Mengo virus specific cytotoxic T lymphocyte (CTL) response was investigated after intraperitoneal infection of mice with the attenuated Mengo virus strain vMC24. A high level of CTL activity was detected in spleen cell cultures obtained from infected C3H/HeJ (H-2k) or C57BL/6 (H-2b) mice after a secondary in vitro stimulation with Mengo virus-infected cells. The CTL activity, which was MHC class I-restricted, was shown to be mediated by CD8+ T cells. Recombinant vaccinia viruses that expressed capsid proteins VP0, VP1 or VP3 were produced and used to identify the protein(s) recognized by the Mengo virus-specific CTLs. In both C3H/HeJ and C57BL/6 mice, analysis of CTL activity against target cells expressing each capsid protein showed that VP0 was the only capsid protein recognized by the CD8+ CTLs. The CTL epitope(s) could be further located in the C-terminal half of VP0, i.e. in capsid protein VP2. Moreover, using unlabelled target cells expressing VP0 as cold competitors, we were able to almost completely inhibit recognition and lysis of Mengo virus-infected cells by specific CD8+ CTLs. Thus, the CTL response directed against VP2 was immunodominant in both C3H/HeJ- and C57BL/6-infected mice.
用减毒的Mengo病毒株vMC24腹腔感染小鼠后,研究了Mengo病毒特异性细胞毒性T淋巴细胞(CTL)反应。在用Mengo病毒感染的细胞进行二次体外刺激后,在从感染的C3H/HeJ(H-2k)或C57BL/6(H-2b)小鼠获得的脾细胞培养物中检测到高水平的CTL活性。CTL活性受MHC I类限制,显示由CD8 + T细胞介导。生产了表达衣壳蛋白VP0、VP1或VP3的重组痘苗病毒,并用于鉴定Mengo病毒特异性CTL识别的蛋白。在C3H/HeJ和C57BL/6小鼠中,针对表达每种衣壳蛋白的靶细胞的CTL活性分析表明,VP0是CD8 + CTL识别的唯一衣壳蛋白。CTL表位可进一步定位于VP0的C末端一半,即衣壳蛋白VP2中。此外,使用表达VP0的未标记靶细胞作为冷竞争者,我们能够几乎完全抑制特异性CD8 + CTL对Mengo病毒感染细胞的识别和裂解。因此,针对VP2的CTL反应在C3H/HeJ和C57BL/6感染的小鼠中均占主导地位。