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Negative Impact of IFN-γ on Early Host Immune Responses to Retroviral Infection

机译:IFN-γ对逆转录病毒感染的早期宿主免疫反应的负面影响

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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.
机译:免疫系统的任务是防御各种微生物感染,并且与其他微生物的共感染可能强烈影响其对特定传染性微生物的反应。结果表明,小鼠乳酸脱氢酶升高病毒(LDV)感染损害了对Friend病毒(FV)共感染的早期适应性免疫反应。为了研究这种损伤的机制,我们检查了LDV诱导的先天免疫应答,并发现了LDV特异性诱导的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,但是出乎意料的是,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。确定了两种不同的作用。首先,LDV诱导的IFN-γ信号间接调节FV特异性CD8 + T细胞反应。其次,尽管生发中心的形成和中和抗体的产生得到了促进,但B细胞中固有的IFN-γ信号仍促进了多克隆B细胞的活化并增强了早期FV感染。该模型的结果表明,IFN-γ的产生可能会对早期的适应性免疫反应和病毒控制产生不利影响。

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