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嗅球和下丘脑对流感病毒的急性期反应:免疫接种的影响。

Olfactory bulb and hypothalamic acute-phase responses to influenza virus: effects of immunization.

机构信息

Sleep and Performance Research Center and WWAMI Medical Education Program, Washington State University, Spokane, Wash., USA.

出版信息

Neuroimmunomodulation. 2013;20(6):323-33. doi: 10.1159/000351716. Epub 2013 Aug 16.

Abstract

BACKGROUND

Within hours of intranasal challenge, mouse-adapted H1N1 A/Puerto Rico/8/34 (PR8) influenza genomic RNA is found in the olfactory bulb (OB) and OB pro-inflammatory cytokines are up-regulated. Severing the olfactory tract delays the acute-phase response (APR) and the APR is attenuated by immunization.

OBJECTIVES

To determine if immunization affects OB localization of influenza or the molecular brain mechanisms regulating APR.

METHODS

Male mice were immunized with PR8 influenza, then OB viral RNA, APR, and influenza-related cytokine responses were determined after homologous viral challenge.

RESULTS

Immunization did not prevent influenza OB viral invasion within 24 h of viral challenge. However, it greatly attenuated OB viral RNA 6 days after viral challenge and the APR including hypothermia and body weight loss responses. Within the OB, 24 h after influenza challenge, prior immunization blocked virus-induced up-regulation of toll-like receptor 7 and interferon (IFN) γ mRNAs. At this time, hypothalamic (HT) growth hormone-releasing hormone receptor and tumor necrosis factor-α mRNAs were greatly enhanced in immunized but not in positive control mice. By 6 days after viral challenge, OB and HT mRNAs returned towards baseline values. In the lung, mRNA up-regulation was greater than that in the brain and maximized 6 days after challenge. Lung IFNγ mRNA decreased at 24 h but increased 6 days after challenge in the positive compared to negative controls. Immunization prevented the up-regulation of most of the flu-related mRNAs measured in lungs.

CONCLUSION

Collectively, these data suggest a role for OB and HT involvement in immunization protection against influenza infection.

摘要

背景

鼻内接种后数小时内,适应小鼠的 H1N1 A/波多黎各/8/34(PR8)流感基因组 RNA 可在嗅球(OB)中检测到,OB 促炎细胞因子上调。切断嗅神经可延迟急性相反应(APR),而免疫接种可减弱 APR。

目的

确定免疫接种是否影响流感在 OB 中的定位或调节 APR 的分子脑机制。

方法

雄性小鼠用 PR8 流感免疫,然后在同源病毒攻击后测定 OB 病毒 RNA、APR 和与流感相关的细胞因子反应。

结果

免疫接种并不能预防病毒攻击后 24 小时内 OB 中的流感病毒入侵。然而,它大大减弱了 OB 中病毒 RNA 6 天后的水平以及 APR,包括体温下降和体重减轻反应。在流感攻击后 24 小时内,先前的免疫接种阻止了病毒诱导的 TLR7 和 IFNγ mRNA 的上调。此时,免疫接种小鼠的下丘脑(HT)生长激素释放激素受体和肿瘤坏死因子-α mRNA 大大增强,但阳性对照小鼠则没有。6 天后,OB 和 HT mRNA 恢复到基线值。在肺部,mRNA 的上调程度大于大脑,且在攻击后 6 天达到最大值。与阴性对照相比,肺部 IFNγ mRNA 在 24 小时时下调,但在 6 天后增加。免疫接种可防止肺部测量的大多数与流感相关的 mRNA 上调。

结论

综上所述,这些数据表明 OB 和 HT 参与了免疫接种对流感感染的保护作用。

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