Tarr Andrew J, Liu Xiaoyu, Reed Nathaniel S, Quan Ning
Division of Biosciences, The Ohio State University, 305 W. 12th Ave, Columbus, OH 43210, USA; Institute for Behavioral Medicine Research, The Ohio State University Wexner Medical Center, 460 Medical Center Dr., Columbus, OH 43210, USA.
Division of Biosciences, The Ohio State University, 305 W. 12th Ave, Columbus, OH 43210, USA; Institute for Behavioral Medicine Research, The Ohio State University Wexner Medical Center, 460 Medical Center Dr., Columbus, OH 43210, USA.
Brain Behav Immun. 2014 Nov;42:96-108. doi: 10.1016/j.bbi.2014.06.002. Epub 2014 Jun 12.
We found recently that controlled progressive challenge with subthreshold levels of E. coli can confer progressively stronger resistance to future reinfection-induced sickness behavior to the host. We have termed this type of inflammation "euflammation". In this study, we further characterized the kinetic changes in the behavior, immunological, and neuroendocrine aspects of euflammation. Results show euflammatory animals only display transient and subtle sickness behaviors of anorexia, adipsia, and anhedonia upon a later infectious challenge which would have caused much more severe and longer lasting sickness behavior if given without prior euflammatory challenges. Similarly, infectious challenge-induced corticosterone secretion was greatly ameliorated in euflammatory animals. At the site of E.coli priming injections, which we termed euflammation induction locus (EIL), innate immune cells displayed a partial endotoxin tolerant phenotype with reduced expression of innate activation markers and muted inflammatory cytokine expression upon ex vivo LPS stimulation, whereas innate immune cells outside EIL displayed largely opposite characteristics. Bacterial clearance function, however, was enhanced both inside and outside EIL. Finally, sickness induction by an infectious challenge placed outside the EIL was also abrogated. These results suggest euflammation could be used as an efficient method to "train" the innate immune system to resist the consequences of future infectious/inflammatory challenges.
我们最近发现,用亚阈值水平的大肠杆菌进行可控的渐进性刺激,可使宿主对未来再感染诱发的疾病行为产生逐渐增强的抵抗力。我们将这种炎症类型称为“良性炎症”。在本研究中,我们进一步对良性炎症在行为、免疫和神经内分泌方面的动力学变化进行了表征。结果显示,经历过良性炎症的动物在随后的感染性刺激时,仅表现出短暂且轻微的疾病行为,如厌食、拒饮和快感缺失,而如果没有先前的良性炎症刺激,同样的感染性刺激会导致更严重且持续时间更长的疾病行为。同样,感染性刺激诱导的促肾上腺皮质激素分泌在经历过良性炎症的动物中也得到了极大改善。在我们称为良性炎症诱导位点(EIL)的大肠杆菌初次注射部位,固有免疫细胞表现出部分内毒素耐受表型,在体外脂多糖刺激下,固有激活标志物的表达降低,炎症细胞因子表达减弱,而EIL以外的固有免疫细胞则表现出大致相反的特征。然而,EIL内外的细菌清除功能均得到增强。最后,在EIL以外部位进行的感染性刺激诱导疾病的情况也被消除。这些结果表明,良性炎症可作为一种有效的方法来“训练”固有免疫系统,以抵抗未来感染/炎症刺激的后果。