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Treponema pallidum (syphilis) antigen TpF1 induces angiogenesis through the activation of the IL-8 pathway

机译:梅毒螺旋体(梅毒)抗原TpF1通过激活IL-8途径诱导血管生成

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摘要

Over 10 million people every year become infected by Treponema pallidum and develop syphilis, a disease with broad symptomatology that, due to the difficulty to eradicate the pathogen from the highly vascularized secondary sites of infection, is still treated with injections of penicillin. Unlike most other bacterial pathogens, T. pallidum infection produces indeed a strong angiogenic response whose mechanism of activation, however, remains unknown. Here, we report that one of the major antigen of T. pallidum, the TpF1 protein, has growth factor-like activity on primary cultures of human endothelial cells and activates specific T cells able to promote tissue factor production. The growth factor-like activity is mediated by the secretion of IL-8 but not of VEGF, two known angiogenic factors. The pathogen’s factor signals IL-8 secretion through the activation of the CREB/NF-κB signalling pathway. These findings are recapitulated in an animal model, zebrafish, where we observed that TpF1 injection stimulates angiogenesis and IL-8, but not VEGF, secretion. This study suggests that the angiogenic response observed during secondary syphilis is triggered by TpF1 and that pharmacological therapies directed to inhibit IL-8 response in patients should be explored to treat this disease.
机译:每年有超过一千万的人被梅毒螺旋体感染并发展为梅毒。梅毒是一种症状广泛的疾病,由于难以从高度血管化的继发感染部位清除病原体,因此仍需注射青霉素治疗。与大多数其他细菌性病原体不同,苍白锥虫感染确实产生了强烈的血管生成反应,但其激活机制尚不清楚。在这里,我们报告苍白衣原体的主要抗原之一,TpF1蛋白,对人内皮细胞的原代培养具有生长因子样活性,并激活能够促进组织因子产生的特定T细胞。类生长因子的活性是由IL-8的分泌介导的,而不是由VEGF,这是两个已知的血管生成因子介导的。病原体因子通过激活CREB ​​/NF-κB信号通路来表达IL-8分泌。这些发现在动物模型斑马鱼中得到了概括,在该模型中我们观察到TpF1注射刺激血管生成和IL-8分泌,但不刺激VEGF分泌。这项研究表明,继发性梅毒期间观察到的血管生成反应是由TpF1触发的,应该探索针对患者中抑制IL-8反应的药理疗法。

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