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IL2-330G polymorphic allele is associated with decreased risk of Helicobacter pylori infection in adulthood
We evaluated whether polymorphisms in genes coding molecules linked to the innate and adaptive immune response are associated with susceptibility to Helicobacter pylori infection. IL1B-511C → T, IL1B-31 T → C, IL1RN allele 2, IL2-330 T → G, TNFA-307 G → A, TLR2Arg677Trp, TLR2Arg753Gln, TLR4Asp299Gly...
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Published in: | Microbes and infection 2009-10, Vol.11 (12), p.980-987 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | We evaluated whether polymorphisms in genes coding molecules linked to the innate and adaptive immune response are associated with susceptibility to
Helicobacter pylori infection.
IL1B-511C
→
T,
IL1B-31
T
→
C,
IL1RN allele 2,
IL2-330
T
→
G,
TNFA-307
G
→
A,
TLR2Arg677Trp,
TLR2Arg753Gln,
TLR4Asp299Gly, and
TLR5
392STOP polymorphisms were determined in 541 blood donors.
IL2-330
T
→
G allele carriers had a decreased
H. pylori infection risk (OR
=
0.63, 95% CI
=
0.43–0.93) after adjustment for demographic and environmental factors. Hence, we investigated whether the polymorphism is functional by evaluating IL-2 serum concentration in 150 blood donors and 100 children. IL-2 pro-inflammatory and anti-inflammatory properties were indirectly investigated by determining serum IFN-γ and IL-10/TGF-β levels. The polymorphism was associated with increased mean IL-2 levels in
H. pylori-positive adults (2.65
pg/mL vs. 7.78
pg/mL) and children (4.19
pg/mL vs. 8.03
pg/mL). Increased IL-2 was associated with pro-inflammatory activity in adults (IFN-γ
=
18.61
pg/mL vs. 25.71
pg/mL), and with anti-inflammatory activity in children (IL-10
=
6.99 vs. 14.17
pg/mL, TGF-β
=
45.88 vs. 93.44
pg/mL) (
p
<
10
−3 for all). In conclusion, in the context of
H. pylori infection,
IL2-330
T
→
G polymorphism is functional and is associated with decreased risk of infection in adults. |
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ISSN: | 1286-4579 1769-714X |
DOI: | 10.1016/j.micinf.2009.07.008 |