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      Helicobacter pylori vacuolating cytotoxin inhibits T lymphocyte activation.

      Science (New York, N.Y.)
      Apoptosis, Bacterial Proteins, pharmacology, physiology, Bacterial Toxins, Calcineurin, metabolism, Calcineurin Inhibitors, Cyclins, Cytotoxins, DNA-Binding Proteins, genetics, G1 Phase, Gene Expression Regulation, HeLa Cells, Helicobacter pylori, pathogenicity, Humans, Interleukin-2, Jurkat Cells, Lymphocyte Activation, NFATC Transcription Factors, Nuclear Proteins, Oligonucleotide Array Sequence Analysis, S Phase, Signal Transduction, T-Lymphocytes, immunology, microbiology, Tacrolimus, Transcription Factors, Transcription, Genetic, Transfection

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          Abstract

          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 G1/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 down-regulation 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.

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