Käbisch Romy, Semper Raphaela P, Wüstner Stefanie, Gerhard Markus, Mejías-Luque Raquel
Institut für Medizinische Mikrobiologie, Immunologie und Hygiene, Technische Universität München, 81675 Munich, Germany; and.
Institut für Medizinische Mikrobiologie, Immunologie und Hygiene, Technische Universität München, 81675 Munich, Germany; and German Centre for Infection Research, 81675 Munich, Germany.
J Immunol. 2016 May 15;196(10):4246-52. doi: 10.4049/jimmunol.1501062. Epub 2016 Apr 18.
Helicobacter pylori infection is characterized by chronic persistence of the bacterium. Different virulence factors, including H. pylori γ-glutamyltranspeptidase (gGT), have been reported to induce tolerogenicity by reprogramming dendritic cells (DCs). gGT is present in all bacterial isolates, indicating an important role for gGT in the course of infection. In the current study, we have analyzed the effect of H. pylori gGT on human DCs and the subsequent adaptive immune response. We show that glutamate produced due to H. pylori gGT enzymatic activity tolerizes DCs by inhibiting cAMP signaling and dampening IL-6 secretion in response to the infection. Together, our results provide a novel molecular mechanism by which H. pylori manipulates the host's immune response to persist within its host.
幽门螺杆菌感染的特征是该细菌的慢性持续存在。据报道,包括幽门螺杆菌γ-谷氨酰转肽酶(gGT)在内的不同毒力因子可通过重编程树突状细胞(DCs)来诱导耐受性。gGT存在于所有细菌分离株中,表明gGT在感染过程中起重要作用。在本研究中,我们分析了幽门螺杆菌gGT对人DCs的影响以及随后的适应性免疫反应。我们发现,由于幽门螺杆菌gGT的酶活性产生的谷氨酸通过抑制cAMP信号传导并抑制感染后IL-6的分泌,从而使DCs产生耐受性。总之,我们的结果提供了一种新的分子机制,幽门螺杆菌通过该机制操纵宿主的免疫反应以在宿主体内持续存在。