Gebert B, Fischer W, Haas R
Max von Pettenkofer Institut für Hygiene und Medizinische Mikrobiologie, LMU München Pettenkoferstr., München, Germany.
Rev Physiol Biochem Pharmacol. 2004;152:205-20. doi: 10.1007/s10254-004-0027-3. Epub 2004 Jul 27.
Helicobacter pylori is a highly successful bacterial pathogen of humans, infecting the stomach of more than half of the world's population. The H. pylori infection results in chronic gastritis, eventually followed by peptic ulceration and, more rarely, gastric cancer. H. pylori has developed a unique set of virulence factors, actively supporting its survival in the special ecological niche of the human stomach. Vacuolating cytotoxin (VacA) and cytotoxin-associated antigen A (CagA) are two major bacterial virulence factors involved in host cell modulation. VacA, so far mainly regarded as a cytotoxin of the gastric epithelial cell layer, now turns out to be a potent immunomodulatory toxin, targeting the adapted immune system. Thus, in addition to the well-known vacuolating activity, VacA has been reported to induce apoptosis in epithelial cells, to affect B lymphocyte antigen presentation, to inhibit the activation and proliferation of T lymphocytes, and to modulate the T cell-mediated cytokine response.
幽门螺杆菌是一种非常成功的人类细菌病原体,感染了世界上超过一半人口的胃部。幽门螺杆菌感染会导致慢性胃炎,最终发展为消化性溃疡,更罕见的情况下会引发胃癌。幽门螺杆菌已经形成了一套独特的毒力因子,积极支持其在人类胃部特殊生态位中的生存。空泡毒素(VacA)和细胞毒素相关抗原A(CagA)是参与宿主细胞调节的两种主要细菌毒力因子。VacA迄今为止主要被视为胃上皮细胞层的一种细胞毒素,现在发现它是一种强效的免疫调节毒素,可以靶向适应性免疫系统。因此,除了众所周知的空泡形成活性外,据报道VacA还能诱导上皮细胞凋亡,影响B淋巴细胞抗原呈递,抑制T淋巴细胞的激活和增殖,并调节T细胞介导的细胞因子反应。