Matera Giovanni, Liberto Maria Carla, Joosten Leo A B, Vinci Maria, Quirino Angela, Pulicari Maria Concetta, Kullberg Bart Jan, Van der Meer Jos W M, Netea Mihai G, Focà Alfredo
Institute of Microbiology, Department of Medical Sciences, University Magna Graecia, Via T. Campanella 115, 88100 Catanzaro, Italy.
Eur Cytokine Netw. 2008 Sep;19(3):113-8. doi: 10.1684/ecn.2008.0128. Epub 2008 Sep 8.
Bartonella quintana (B. quintana) is a facultative, intracellular bacterium, which causes trench fever, chronic bacteraemia and bacillary angiomatosis. Little is known about the recognition of B. quintana by the innate immune system. In this review, we address the impact of Toll-like receptors (TLRs) on the recognition of B. quintana and the activation of the host defense. When experimental models using human mononuclear cells, transfected CHO cells, or TLR2-/- and TLR4-/- mice were used, differential effects of TLR2 and TLR4 have been observed. B. quintana micro-organisms stimulated cytokine production through TLR2-mediated signals, whereas no role for TLR4 in the recognition of this pathogen was observed. When single, water-phenol extraction was performed, B. quintana LPS, stimulated cytokine production in a TLR2-dependent manner. However, when double extraction was performed in order to generate highly purified LPS, B. quintana LPS entirely lost its capacity to stimulate cytokines, demonstrating that non-LPS components of B. quintana are responsible for the recognition through TLR2. Moreover, B. quintana LPS was shown to be a potent antagonist of Toll-like receptor 4 (TLR4). In conclusion, B. quintana is an inducer of cytokines through TLR2-, but not TLR4-, dependent mechanisms. This stimulation is induced by bacterial components other than lipopolysaccharide. B. quintana LPS is a naturally occurring antagonist of Toll-like receptor 4 (TLR4). In view of the role played by TLR4 in inflammation, B. quintana LPS may be useful as an anti-TLR4 agent with therapeutic potential in both infections and autoimmune inflammation.
五日热巴尔通体(B. quintana)是一种兼性细胞内细菌,可引起战壕热、慢性菌血症和杆菌性血管瘤病。关于固有免疫系统对五日热巴尔通体的识别了解甚少。在本综述中,我们探讨了 Toll 样受体(TLR)对五日热巴尔通体识别及宿主防御激活的影响。当使用人单核细胞、转染的 CHO 细胞或 TLR2 - / - 和 TLR4 - / - 小鼠的实验模型时,观察到了 TLR2 和 TLR4 的不同作用。五日热巴尔通体微生物通过 TLR2 介导的信号刺激细胞因子产生,而未观察到 TLR4 在识别该病原体中发挥作用。当进行单步水 - 酚提取时,五日热巴尔通体脂多糖(LPS)以 TLR2 依赖的方式刺激细胞因子产生。然而,当进行双步提取以生成高度纯化的 LPS 时,五日热巴尔通体 LPS 完全丧失了刺激细胞因子的能力,这表明五日热巴尔通体的非 LPS 成分负责通过 TLR2 进行识别。此外,五日热巴尔通体 LPS 被证明是 Toll 样受体 4(TLR4)的有效拮抗剂。总之,五日热巴尔通体是通过 TLR2 而非 TLR4 依赖的机制诱导细胞因子产生的。这种刺激是由脂多糖以外的细菌成分诱导的。五日热巴尔通体 LPS 是 Toll 样受体 4(TLR4)的天然拮抗剂。鉴于 TLR4 在炎症中所起的作用,五日热巴尔通体 LPS 可能作为一种抗 TLR4 药物,在感染和自身免疫性炎症中具有治疗潜力。