Coleman Fadie T, Blahna Matthew T, Kamata Hirofumi, Yamamoto Kazuko, Zabinski Mary C, Kramnik Igor, Wilson Andrew A, Kotton Darrell N, Quinton Lee J, Jones Matthew R, Pelton Stephen I, Mizgerd Joseph P
Pulmonary Center.
Department of Microbiology.
J Infect Dis. 2017 Aug 15;216(4):425-435. doi: 10.1093/infdis/jix159.
During pneumococcal pneumonia, antibacterial defense requires the orchestrated expression of innate immunity mediators, initiated by alveolar macrophages and dependent on transcription driven by nuclear factor κB (NF-κB). Such immune pressure may select for pneumococci, which avoid or subvert macrophage NF-κB activation. Analyzing pneumococci collected from children in Massachusetts, we found that the activation of macrophage NF-κB by Streptococcus pneumoniae is highly diverse, with a preponderance of low NF-κB activators that associate particularly with complicated pneumonia. Low NF-κB activators cause more severe lung infections in mice, and they drive macrophages toward an alternate and detrimental cell fate of necroptosis. Both outcomes can be reversed by activation of macrophages with pneumococci that are high NF-κB activators. These results suggest that low NF-κB activation is a virulence property of pneumococci and that the appropriate activation of macrophages, including NF-κB, may hold promise as an adjunct therapeutic avenue for pneumococcal pneumonia.
在肺炎球菌肺炎期间,抗菌防御需要肺泡巨噬细胞启动并依赖于核因子κB(NF-κB)驱动的转录来协调表达先天免疫介质。这种免疫压力可能会筛选出能够避免或破坏巨噬细胞NF-κB激活的肺炎球菌。通过分析从马萨诸塞州儿童身上收集的肺炎球菌,我们发现肺炎链球菌对巨噬细胞NF-κB的激活具有高度多样性,其中低NF-κB激活剂占优势,这些激活剂尤其与复杂性肺炎相关。低NF-κB激活剂在小鼠中会导致更严重的肺部感染,并且会促使巨噬细胞走向坏死性凋亡这一交替且有害的细胞命运。而高NF-κB激活剂的肺炎球菌激活巨噬细胞可逆转这两种结果。这些结果表明,低NF-κB激活是肺炎球菌的一种毒力特性,适当激活巨噬细胞(包括NF-κB)有望成为肺炎球菌肺炎的辅助治疗途径。