Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840, USA.
J Immunol. 2012 Sep 1;189(5):2521-9. doi: 10.4049/jimmunol.1201125. Epub 2012 Jul 20.
The immune system is tasked with defending against a myriad of microbial infections, and its response to a given infectious microbe may be strongly influenced by coinfection with another microbe. It was shown that infection of mice with lactate dehydrogenase-elevating virus (LDV) impairs early adaptive immune responses to Friend virus (FV) coinfection. To investigate the mechanism of this impairment, we examined LDV-induced innate immune responses and found LDV-specific induction of IFN-α and IFN-γ. LDV-induced IFN-α had little effect on FV infection or immune responses, but unexpectedly, LDV-induced IFN-γ production dampened Th1 adaptive immune responses and enhanced FV infection. Two distinct effects were identified. First, LDV-induced IFN-γ signaling indirectly modulated FV-specific CD8+ T cell responses. Second, intrinsic IFN-γ signaling in B cells promoted polyclonal B cell activation and enhanced early FV infection, despite promotion of germinal center formation and neutralizing Ab production. Results from this model reveal that IFN-γ production can have detrimental effects on early adaptive immune responses and virus control.
免疫系统的任务是抵御各种微生物感染,而其对特定感染微生物的反应可能会受到另一种微生物的合并感染的强烈影响。已经表明,感染乳酸脱氢酶升高病毒 (LDV) 会损害对 Friend 病毒 (FV) 合并感染的早期适应性免疫反应。为了研究这种损害的机制,我们检查了 LDV 诱导的先天免疫反应,并发现 LDV 特异性诱导了 IFN-α 和 IFN-γ。LDV 诱导的 IFN-α 对 FV 感染或免疫反应几乎没有影响,但出乎意料的是,LDV 诱导的 IFN-γ 产生抑制了 Th1 适应性免疫反应并增强了 FV 感染。确定了两个不同的影响。首先,LDV 诱导的 IFN-γ 信号间接调节了 FV 特异性 CD8+T 细胞反应。其次,B 细胞中的固有 IFN-γ 信号促进了多克隆 B 细胞激活,并增强了早期 FV 感染,尽管促进了生发中心形成和中和 Ab 产生。该模型的结果表明,IFN-γ 的产生可能对早期适应性免疫反应和病毒控制产生不利影响。