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Lower circulating levels of chemokine CXCL10 in Helicobacter pylori-infected patients with peptic ulcer: Influence of the bacterial virulence factor CagA

BACKGROUND AND OBJECTIVES: Alterations in CXCL10 (a Th1 chemokine) expression have been associated with various diseases. The aim of this study was to evaluate the serum CXCL10 levels in H. pylori-infected patients with peptic ulcer (PU), H. pylori-infected asymptomatic (AS) subjects and healthy H....

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Autores principales: Jafarzadeh, Abdollah, Nemati, Maryam, Rezayati, Mohammad Taghi, Khoramdel, Hossain, Nabizadeh, Mansooreh, Hassanshahi, Gholamhossain, Abdollahi, Hamid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3577565/
https://www.ncbi.nlm.nih.gov/pubmed/23467184
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author Jafarzadeh, Abdollah
Nemati, Maryam
Rezayati, Mohammad Taghi
Khoramdel, Hossain
Nabizadeh, Mansooreh
Hassanshahi, Gholamhossain
Abdollahi, Hamid
author_facet Jafarzadeh, Abdollah
Nemati, Maryam
Rezayati, Mohammad Taghi
Khoramdel, Hossain
Nabizadeh, Mansooreh
Hassanshahi, Gholamhossain
Abdollahi, Hamid
author_sort Jafarzadeh, Abdollah
collection PubMed
description BACKGROUND AND OBJECTIVES: Alterations in CXCL10 (a Th1 chemokine) expression have been associated with various diseases. The aim of this study was to evaluate the serum CXCL10 levels in H. pylori-infected patients with peptic ulcer (PU), H. pylori-infected asymptomatic (AS) subjects and healthy H. pylori-negative subjects, and also to determine its association with bacterial virulence factor cytotoxin-associated gene A (CagA). MATERIALS AND METHODS: Serum samples from 90 H. pylori infected patients with PU (70 were anti-CagA (+), 20 were anti-CagA (-)), 65 AS carriers (40 were anti-CagA (+), 25 were anti-CagA (-)) and 30 healthy H. pylori-negative subjects (as a control group) were tested for concentrations of CXCL10 by using the ELISA method. RESULTS: The mean serum levels of CXCL10 in PU patients (96.64 ± 20.85 pg/mL) were significantly lower than those observed in AS subjects (162.16 ± 53.31 pg/mL, P < 0.01) and the control group (193.93 ± 42.14 pg/mL, P < 0.02). In the PU group, the serum levels of CXCL10 in anti-CagA (+) subjects was significantly higher in comparison to anti-CagA (-) patients (P < 0.04). CONCLUSION: These results showed that the mean concentrations of CXCL10 in H. pylori-infected-PU patients was lower than AS carriers and control group. In the PU group, the serum levels of CXCL10 were associated with bacterial factor CagA.
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spelling pubmed-35775652013-03-06 Lower circulating levels of chemokine CXCL10 in Helicobacter pylori-infected patients with peptic ulcer: Influence of the bacterial virulence factor CagA Jafarzadeh, Abdollah Nemati, Maryam Rezayati, Mohammad Taghi Khoramdel, Hossain Nabizadeh, Mansooreh Hassanshahi, Gholamhossain Abdollahi, Hamid Iran J Microbiol Original Article BACKGROUND AND OBJECTIVES: Alterations in CXCL10 (a Th1 chemokine) expression have been associated with various diseases. The aim of this study was to evaluate the serum CXCL10 levels in H. pylori-infected patients with peptic ulcer (PU), H. pylori-infected asymptomatic (AS) subjects and healthy H. pylori-negative subjects, and also to determine its association with bacterial virulence factor cytotoxin-associated gene A (CagA). MATERIALS AND METHODS: Serum samples from 90 H. pylori infected patients with PU (70 were anti-CagA (+), 20 were anti-CagA (-)), 65 AS carriers (40 were anti-CagA (+), 25 were anti-CagA (-)) and 30 healthy H. pylori-negative subjects (as a control group) were tested for concentrations of CXCL10 by using the ELISA method. RESULTS: The mean serum levels of CXCL10 in PU patients (96.64 ± 20.85 pg/mL) were significantly lower than those observed in AS subjects (162.16 ± 53.31 pg/mL, P < 0.01) and the control group (193.93 ± 42.14 pg/mL, P < 0.02). In the PU group, the serum levels of CXCL10 in anti-CagA (+) subjects was significantly higher in comparison to anti-CagA (-) patients (P < 0.04). CONCLUSION: These results showed that the mean concentrations of CXCL10 in H. pylori-infected-PU patients was lower than AS carriers and control group. In the PU group, the serum levels of CXCL10 were associated with bacterial factor CagA. Tehran University of Medical Sciences 2013-03 /pmc/articles/PMC3577565/ /pubmed/23467184 Text en © 2013 Iranian Society of Microbiology & Tehran University of Medical Sciences http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jafarzadeh, Abdollah
Nemati, Maryam
Rezayati, Mohammad Taghi
Khoramdel, Hossain
Nabizadeh, Mansooreh
Hassanshahi, Gholamhossain
Abdollahi, Hamid
Lower circulating levels of chemokine CXCL10 in Helicobacter pylori-infected patients with peptic ulcer: Influence of the bacterial virulence factor CagA
title Lower circulating levels of chemokine CXCL10 in Helicobacter pylori-infected patients with peptic ulcer: Influence of the bacterial virulence factor CagA
title_full Lower circulating levels of chemokine CXCL10 in Helicobacter pylori-infected patients with peptic ulcer: Influence of the bacterial virulence factor CagA
title_fullStr Lower circulating levels of chemokine CXCL10 in Helicobacter pylori-infected patients with peptic ulcer: Influence of the bacterial virulence factor CagA
title_full_unstemmed Lower circulating levels of chemokine CXCL10 in Helicobacter pylori-infected patients with peptic ulcer: Influence of the bacterial virulence factor CagA
title_short Lower circulating levels of chemokine CXCL10 in Helicobacter pylori-infected patients with peptic ulcer: Influence of the bacterial virulence factor CagA
title_sort lower circulating levels of chemokine cxcl10 in helicobacter pylori-infected patients with peptic ulcer: influence of the bacterial virulence factor caga
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3577565/
https://www.ncbi.nlm.nih.gov/pubmed/23467184
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