Popa Calin, Abdollahi-Roodsaz Shahla, Joosten Leo A B, Takahashi Nozomi, Sprong Tom, Matera Giovanni, Liberto Maria Carla, Foca Alfredo, van Deuren Marcel, Kullberg Bart Jan, van den Berg Wim B, van der Meer Jos W M, Netea Mihai G
Department of General Internal Medicine, Radboud University Nijmegen Medical Centre, The Netherlands.
Infect Immun. 2007 Oct;75(10):4831-7. doi: 10.1128/IAI.00237-07. Epub 2007 Jul 2.
Bartonella quintana is a gram-negative microorganism that causes trench fever and chronic bacteremia. B. quintana lipopolysaccharide (LPS) was unable to induce the production of proinflammatory cytokines in human monocytes. Interestingly, B. quintana LPS is a potent antagonist of Toll-like receptor 4 (TLR4), as it inhibited both mRNA transcription and the release of tumor necrosis factor alpha, interleukin 1beta (IL-1beta), and IL-6 by Escherichia coli LPS in human monocytes, at ratios ranging from 1,000:1 to 10:1 (B. quintana LPS to E. coli LPS). Likewise, B. quintana LPS blocked the interaction of E. coli LPS with TLR4 in transfected cell lines. The extent of the inhibitory effect of B. quintana LPS was demonstrated in microarray studies, which showed downregulation of practically all genes induced by LPS in monocytes. Because of the role of TLR4 in inflammation, B. quintana LPS may prove useful as a potent anti-TLR4 agent with therapeutic potential in both infections and autoimmune inflammation.
五日热巴尔通体是一种革兰氏阴性微生物,可引起战壕热和慢性菌血症。五日热巴尔通体脂多糖(LPS)无法诱导人单核细胞产生促炎细胞因子。有趣的是,五日热巴尔通体LPS是Toll样受体4(TLR4)的强效拮抗剂,因为它能抑制人单核细胞中大肠杆菌LPS诱导的mRNA转录以及肿瘤坏死因子α、白细胞介素1β(IL-1β)和IL-6的释放,比例范围为1000:1至10:1(五日热巴尔通体LPS与大肠杆菌LPS)。同样,五日热巴尔通体LPS在转染细胞系中阻断了大肠杆菌LPS与TLR4的相互作用。微阵列研究证明了五日热巴尔通体LPS的抑制作用程度,该研究显示单核细胞中几乎所有由LPS诱导的基因均下调。由于TLR4在炎症中的作用,五日热巴尔通体LPS可能被证明是一种具有治疗潜力的强效抗TLR4药物,可用于治疗感染和自身免疫性炎症。