Weidinger G, Henning G, ter Meulen V, Niewiesk S
Institute of Virology and Immunobiology, University of Wuerzburg, 97078 Wuerzburg, Germany.
J Virol. 2001 Apr;75(7):3059-65. doi: 10.1128/JVI.75.7.3059-3065.2001.
BALB/c mice are resistant to measles virus (MV)-induced encephalitis due to their strong MV-specific CD4(+) T-cell response. Resistance is broken by neutralization of gamma interferon with monoclonal antibodies, indicating an important role for this pleiotropic cytokine. Here, we demonstrate that mouse gamma interferon has no direct antiviral effect in vitro and in vivo. The breakdown of resistance is due neither to a switch in the T-helper response nor to an impaired migration of CD4(+) T cells. Neutralization of gamma interferon interferes with the major histocompatibility complex class II-dependent antigen presentation and subsequent proliferation of CD4(+) T cells in vitro and in vivo. In consequence, the reduction in numbers of CD4(+) T cells below a protective threshold leads to susceptibility to MV-induced encephalitis.
BALB/c小鼠对麻疹病毒(MV)诱导的脑炎具有抗性,这归因于其强大的MV特异性CD4(+) T细胞反应。用单克隆抗体中和γ干扰素会打破这种抗性,表明这种多效性细胞因子具有重要作用。在此,我们证明小鼠γ干扰素在体外和体内均无直接抗病毒作用。抗性的打破既不是由于辅助性T细胞反应的转变,也不是由于CD4(+) T细胞迁移受损。γ干扰素的中和会干扰体外和体内主要组织相容性复合体II类依赖性抗原呈递以及随后CD4(+) T细胞的增殖。因此,CD4(+) T细胞数量减少至低于保护阈值会导致对MV诱导的脑炎易感。