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Helicobacter pylori vacuolating cytotoxin inhibits T lymphocyte activation

机译:幽门螺杆菌空泡细胞毒素抑制T淋巴细胞活化

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Helicobacter pylori (Hp) vacuolating cytotoxin VacA induces cellular vacuolation in epithelial cells. We found that VacA could efficiently block proliferation of T cells by inducing a G(1)/S cell cycle arrest. It interfered with the T cell receptor/interleukin-2 (IL-2) signaling pathway at the level of the Ca2+-calmodulin-dependent phosphatase calcineurin. Nuclear translocation of nuclear factor of activated T cells (NFAT), a transcription factor acting as a global regulator of immune response genes, was abrogated, resulting in downregulation of IL-2 transcription. VacA partially mimicked the activity of the immunosuppressive drug FK506 by possibly inducing a local immune suppression, explaining the extraordinary chronicity of Hp infections. [References: 25]
机译:幽门螺杆菌(Hp)空泡化细胞毒素VacA在上皮细胞中诱导细胞空泡化。我们发现,VacA可以通过诱导G(1)/ S细胞周期停滞有效地阻止T细胞的增殖。它在Ca2 +-钙调蛋白依赖性磷酸酶钙调神经磷酸酶水平上干扰T细胞受体/白介素2(IL-2)信号通路。废除了活化T细胞核因子(NFAT)的核易位,后者是免疫应答基因的整体调节因子,导致IL-2转录的下调。 VacA可能通过诱导局部免疫抑制来部分模仿免疫抑制药物FK506的活性,从而解释了Hp感染的异常长期性。 [参考:25]

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