| Literature DB >> 10896773 |
B Paziak-Domańska1, M Chmiela, A Jarosińska, W Rudnicka.
Abstract
The pathogenicity of chronic gastroduodenal diseases is very often related to Helicobacter pylori infections. Most H. pylori strains carry the cagA gene encoding an immunodominant 120- to 128-kDa protein which is considered a virulence marker. The majority of CagA-positive H. pylori isolates also produce a 95-kDa protein cytotoxin (VacA) causing vacuolation and degradation of mammalian cells. In our previous study we have shown that live H. pylori bacteria and their sonicates inhibit PHA-driven proliferation of human T lymphocytes. The H. pylori CagA and VacA proteins were suspected of a paralyzing effect of H. pylori on T cell proliferation. In this report, by using isogenic H. pylori mutant strains defective in CagA and VacA proteins, we determined that CagA is responsible for the inhibition of PHA-induced proliferation of T cells. Copyright 2000 Academic Press.Entities:
Mesh:
Substances:
Year: 2000 PMID: 10896773 DOI: 10.1006/cimm.2000.1654
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868