Junior Group Mucosal Infections, Hannover Medical School, Hannover, Germany.
PLoS One. 2012;7(5):e35992. doi: 10.1371/journal.pone.0035992. Epub 2012 May 7.
The intestinal immune system mounts inflammatory responses to pathogens but tolerates harmless commensal microbiota. Various mechanisms for pathogen/non-pathogen discrimination have been proposed but their general relevance for inflammation control is unclear. Here, we compared intestinal responses to pathogenic Salmonella and non-pathogenic E. coli. Both microbes entered intestinal Peyer's patches and, surprisingly, induced qualitatively and quantitatively similar initial inflammatory responses revealing a striking discrimination failure. Diverging inflammatory responses only occurred when Salmonella subsequently proliferated and induced escalating neutrophil infiltration, while harmless E. coli was rapidly cleared from the tissue and inflammation resolved. Transient intestinal inflammation induced by harmless E. coli tolerized against subsequent exposure thereby preventing chronic inflammation during repeated exposure. These data revealed a striking failure of the intestinal immune system to discriminate pathogens from harmless microbes based on distinct molecular signatures. Instead, appropriate intestinal responses to gut microbiota might be ensured by immediate inflammatory responses to any rise in microbial tissue loads, and desensitization after bacterial clearance.
肠道免疫系统会对病原体产生炎症反应,但会对无害共生菌群保持耐受。人们提出了各种用于区分病原体和非病原体的机制,但这些机制对于炎症控制的普遍相关性尚不清楚。在这里,我们比较了肠道对致病性沙门氏菌和非致病性大肠杆菌的反应。这两种微生物都进入了肠道派尔集合淋巴结,令人惊讶的是,它们诱导了定性和定量上相似的初始炎症反应,表明出现了明显的区分失败。只有当沙门氏菌随后增殖并诱导不断增加的中性粒细胞浸润时,才会出现不同的炎症反应,而无害的大肠杆菌很快从组织中清除,炎症得到解决。无害大肠杆菌引起的短暂肠道炎症耐受了随后的暴露,从而防止了在重复暴露期间发生慢性炎症。这些数据揭示了肠道免疫系统在区分病原体和无害微生物方面存在明显的失败,而不是基于明显的分子特征。相反,适当的肠道对肠道微生物群的反应可能是通过对任何微生物组织负荷增加的即时炎症反应,以及在细菌清除后脱敏来确保的。