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卡介苗接种豚鼠对不同分枝杆菌抗原反应的基因特征的时间变化。

Temporal changes in the gene signatures of BCG-vaccinated guinea pigs in response to different mycobacterial antigens.

机构信息

Health Protection Agency, Centre for Emergency Preparedness and Response, Porton Down, Salisbury, Wiltshire SP4 OJG, UK.

出版信息

Vaccine. 2010 Nov 23;28(50):7979-86. doi: 10.1016/j.vaccine.2010.09.061. Epub 2010 Oct 23.

Abstract

Mycobacterium bovis BCG-vaccination in the guinea pig model of tuberculosis (TB) is sufficiently protective that candidate TB vaccines are judged against this. Little is understood about how the BCG vaccine works and, in the absence of a definitive correlate of protection, it is difficult to interpret the significance of novel vaccine induced host responses. Here an extended custom-made microarray (86 guinea pig genes) was used to dissect temporal changes in BCG-vaccine induced gene signatures to different mycobacterial antigens. Initially at 4h, pro-inflammatory genes such as IL-1α, IL-1β, IL-8 and GRO were up-regulated (P<0.001) and these were then superseded by IFN-γ and GM-CSF (at 12 and 20h) post-stimulation, ex vivo with PPD. Similar genes were seen following stimulation with viable BCG but with the addition of IL-23 (P<0.01) after 8h. Our results suggest that temporal changes in the up- and down-regulation of a variety of genes are required to trigger a successful protective response to TB in guinea pigs. This provides base-line information against which new TB vaccines can be compared.

摘要

牛型分枝杆菌卡介苗(BCG)疫苗在结核病(TB)豚鼠模型中具有足够的保护作用,因此候选 TB 疫苗以此为评判标准。人们对 BCG 疫苗的作用机制知之甚少,而且在缺乏明确的保护相关因素的情况下,很难解释新型疫苗诱导的宿主反应的意义。在这里,我们使用了一个扩展的定制微阵列(86 个豚鼠基因)来剖析 BCG 疫苗诱导的基因特征在不同分枝杆菌抗原下的时间变化。最初在 4 小时时,促炎基因(如 IL-1α、IL-1β、IL-8 和 GRO)被上调(P<0.001),然后在刺激后 12 小时和 20 小时被 IFN-γ 和 GM-CSF 取代(PPD 体外)。在刺激活的 BCG 时也观察到了类似的基因,但在 8 小时后添加了 IL-23(P<0.01)。我们的研究结果表明,需要触发豚鼠对结核病的成功保护反应,从而导致各种基因的上调和下调的时间变化。这为新的结核病疫苗提供了基准信息。

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