Literature DB >> 10759250

Serologic response to lower-molecular-weight proteins of H. pylori is related to clinical outcome of H. pylori infection in Taiwan.

S C Shiesh1, B S Sheu, H B Yang, H J Tsao, X Z Lin.   

Abstract

The study aimed to examine the serum serological response among H. pylori-infected patients with various upper gastrointestinal diagnoses; to ascertain whether it could be predictive to the diagnostic outcome of dyspepsia. One hundred seventy H. pylori-infected patients with dyspeptic symptoms but without previous treatment were enrolled, including those with duodenal ulcer disease (N = 47), gastric ulcer (N = 23), nonulcer dyspepsia (N = 60), gastric cancer (N = 34), and MALToma (N = 6). Sera from dyspeptic patients without H. pylori infection (N = 33) were used as controls. During endoscopy, gastric biopsies were taken for CLO-test, histology, and culture for the detection of H. pylori infection, defined by a positive culture or positive results of both CLO-test and histology. Total H. pylori IgG antibody was tested by an ELISA method. Antibody responses to specific H. pylori proteins were tested by a western blotting system. Of patients with H. pylori-infected gastroduodenal diseases, 76.5%, 42.9%, 23.6%, 46.7%, 84.1%, 76.5%, 82.9%, and 32.4% on average, showed responses to the 116-kDa (CagA), 89-kDa (VacA), 60-kDa, 45-kDa, 35-kDa, 30-kDa, 26.5-kDa, and 19.5-kDa H. pylori-specific proteins, respectively. A significant association was found between the serological response to 19.5-kDa and 26.5-kDa proteins and malignant outcome of H. pylori infection (P<0.02). Among patients without malignancy, the absence of a band at 19.5 kDa was statistically associated with the presence of an ulcer (P<0.05). The presence of serum antibody against CagA is not different between patients with ulcer and with malignancy in clinical diagnosis. The serum test for detecting antibodies against lower-molecular-weight proteins of H. pylori, such as those of 19.5 and 26.5 kDa, could be useful to identify H. pylori-infected patients at risk of peptic ulcer or malignancy.

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Year:  2000        PMID: 10759250     DOI: 10.1023/a:1005460130305

Source DB:  PubMed          Journal:  Dig Dis Sci        ISSN: 0163-2116            Impact factor:   3.199


  34 in total

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Journal:  Infect Immun       Date:  1990-03       Impact factor: 3.441

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  10 in total

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Authors:  Z Khodaii; S M H Ghaderian; R Akbarzadeh Najar; H Nejati; A S Tabatabaei Panah
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2.  Evaluation of the role of H pylori infection in pathogenesis of gastric cancer by immunoblot assay.

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3.  Crystal structure of oxidized flavodoxin, an essential protein in Helicobacter pylori.

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4.  A study of recombinant protective H.pylori antigens.

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5.  Diagnosis of Helicobacter pylori infection and diseases associated with Helicobacter pylori by Helicobacter pylori outer membrane proteins.

Authors:  Zheng Jiang; Ai-Long Huang; Xiao-Hong Tao; Pi-Long Wang
Journal:  World J Gastroenterol       Date:  2004-12-01       Impact factor: 5.742

Review 6.  Research progress on Helicobacter pylori outer membrane protein.

Authors:  Shi-He Shao; Hua Wang; Shun-Gen Chai; Li-Mei Liu
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7.  Helicobacter pylori-specific immune responses of children: implications for future vaccination strategy.

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Journal:  Clin Diagn Lab Immunol       Date:  2002-09

8.  Construction and characterization of bivalent vaccine candidate expressing HspA and M(r)18,000 OMP from Helicobacter pylori.

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Journal:  World J Gastroenterol       Date:  2003-08       Impact factor: 5.742

9.  cagA and vacA genotype of Helicobacter pylori associated with gastric diseases in Xi'an area.

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Journal:  World J Gastroenterol       Date:  2003-08       Impact factor: 5.742

10.  Cloning and sequence analysis of gene oipA encoding an outer membrane protein of human Helicobacter pylori.

Authors:  Dao-Rong Chen; Ai-Long Huang; Xiao-Hong Tao; Pi-Long Wang; Zheng Jiang
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  10 in total

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