Molecular detection of host cytokine expression in Helicobacter pylori infected patients via semi-quantitative RT-PCR
Background: Helicobacter pylori (Hp) is a bacterium recognised as a main causative agent for the development of chronic active gastritis, peptic ulcer disease, gastric adenocarcinoma and primary gastric lymphoma. Objective: Determination of the levels of IFN-γ (pro-inflammatory) and IL-4 (anti infla...
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Veröffentlicht in: | Indian journal of medical microbiology 2010-01, Vol.28 (1), p.40-44 |
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Zusammenfassung: | Background: Helicobacter pylori (Hp) is a bacterium recognised as a
main causative agent for the development of chronic active gastritis,
peptic ulcer disease, gastric adenocarcinoma and primary gastric
lymphoma. Objective: Determination of the levels of IFN-γ
(pro-inflammatory) and IL-4 (anti inflammatory) cytokine expression as
indicators of Th1 and Th2 immune responses in gastric cancer (GC) and
non gastric cancer (Non GC) dyspeptic patients by gene specific RT-PCR.
Materials and Methods: Biopsy specimens were collected from three
groups of gastric cancer (GC=18), non ulcer dyspepsia (NUD = 38) and
peptic ulcer patients (PUD=20). Total RNA was extracted and
complementary DNA was synthesised. PCR amplification was performed for
HPRT, IFN-γ and IL-4 cytokines and the intensity of each band was
measured by densitometry and normalized against HPRT expression as a
house keeping gene. Results: Comparison of the results from different
groups of patients indicated that IFN-γ gene expression was
similar in nonGC dyspeptic patients (NUD and PUD groups; 3.38 ±
0.57,3.43 ± 0.41, respectively) whereas, in GC patients, it was
significantly higher than others (5.52 ± 0.59; P < 0.0001). On
the other hand, IL-4 gene expression showed no significant difference
between NUD and GC patients (2.81 ± 0.43,2.3 ± 0.12
respectively), whereas the expression rate of this cytokine was
significantly higher in PUD patients (3.7 ± 0.1; P 0.05). Our data
indicate an association between Th1 and Th2 immune responses and the
development of gastric cancer and peptic ulcer disease respectively. |
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ISSN: | 0255-0857 1998-3646 |
DOI: | 10.4103/0255-0857.58727 |