Sex-specific effects of TLR9 promoter variants on spontaneous clearance of HCV infection. Issue 10 (21st April 2016)
- Record Type:
- Journal Article
- Title:
- Sex-specific effects of TLR9 promoter variants on spontaneous clearance of HCV infection. Issue 10 (21st April 2016)
- Main Title:
- Sex-specific effects of TLR9 promoter variants on spontaneous clearance of HCV infection
- Authors:
- Fischer, Janett
Weber, Alexander N R
Böhm, Stephan
Dickhöfer, Sabine
El Maadidi, Souhayla
Deichsel, Danilo
Knop, Viola
Klinker, Hartwig
Möller, Bernd
Rasenack, Jens
Wang, Lisa
Sharma, Manu
Hinrichsen, Holger
Spengler, Ulrich
Buggisch, Peter
Sarrazin, Christoph
Pawlita, Michael
Waterboer, Tim
Wiese, Manfred
Probst-Müller, Elsbeth
Malinverni, Raffaele
Bochud, Pierre-Yves
Gardiner, Clair
O'Farrelly, Cliona
Berg, Thomas - Abstract:
- Abstract : Objective: As pathogen sensors, Toll-like receptors (TLR) play a role in the first defence line during HCV infection. However, the impact of the DNA sensor TLR9 on the natural course of HCV infection is unknown. To address this, TLR9 promoter polymorphisms (single nucleotide polymorphisms (SNPs)) rs187084 and rs5743836 were investigated for their effect on disease progression. Design: Therefore, the TLR9 SNPs and the interferon lambda 4 ( IFNL4 ) rs12979860 were genotyped in chronically HCV type 1 infected (n=333), in patients who spontaneously cleared the infection (n=161), in the Swiss HCV cohort (n=1057) and the well-characterised German (n=305) and Irish (n=198) 'anti-D' cohorts. Functional analyses were done with promoter reporter constructs of human TLR9 in B cells and assessing TLR9 mRNA levels in whole blood of healthy volunteers. Results: The TLR9 rs187084 C allele was associated with spontaneous virus clearance in women of the study cohort (OR=2.15 (95% CI 1.18 to 3.90) p=0.012), of the Swiss HCV cohort (OR=2.06 (95% CI 1.02 to 4.18) p=0.044) and in both 'anti-D' cohorts (German: OR=2.01 (95% CI 1.14 to 3.55) p=0.016; Irish: OR=1.93 (95% CI 1.10 to 3.68) p=0.047). Multivariate analysis in the combined study and Swiss HCV cohorts supported the results (OR=1.99 (95% CI 1.30 to 3.05) p=0.002). Functional analyses revealed higher transcriptional activities for both TLR9 variants and an association of the C allele of rs5743836 with allele-specific TLR9 mRNAAbstract : Objective: As pathogen sensors, Toll-like receptors (TLR) play a role in the first defence line during HCV infection. However, the impact of the DNA sensor TLR9 on the natural course of HCV infection is unknown. To address this, TLR9 promoter polymorphisms (single nucleotide polymorphisms (SNPs)) rs187084 and rs5743836 were investigated for their effect on disease progression. Design: Therefore, the TLR9 SNPs and the interferon lambda 4 ( IFNL4 ) rs12979860 were genotyped in chronically HCV type 1 infected (n=333), in patients who spontaneously cleared the infection (n=161), in the Swiss HCV cohort (n=1057) and the well-characterised German (n=305) and Irish (n=198) 'anti-D' cohorts. Functional analyses were done with promoter reporter constructs of human TLR9 in B cells and assessing TLR9 mRNA levels in whole blood of healthy volunteers. Results: The TLR9 rs187084 C allele was associated with spontaneous virus clearance in women of the study cohort (OR=2.15 (95% CI 1.18 to 3.90) p=0.012), of the Swiss HCV cohort (OR=2.06 (95% CI 1.02 to 4.18) p=0.044) and in both 'anti-D' cohorts (German: OR=2.01 (95% CI 1.14 to 3.55) p=0.016; Irish: OR=1.93 (95% CI 1.10 to 3.68) p=0.047). Multivariate analysis in the combined study and Swiss HCV cohorts supported the results (OR=1.99 (95% CI 1.30 to 3.05) p=0.002). Functional analyses revealed higher transcriptional activities for both TLR9 variants and an association of the C allele of rs5743836 with allele-specific TLR9 mRNA regulation by oestrogens in women. Conclusions: TLR9 promoter SNPs are associated with the natural course of HCV infection and show higher transcriptional activities. Our results imply the DNA sensor TLR9 in natural immunity against the RNA virus, HCV. … (more)
- Is Part Of:
- Gut. Volume 66:Issue 10(2017)
- Journal:
- Gut
- Issue:
- Volume 66:Issue 10(2017)
- Issue Display:
- Volume 66, Issue 10 (2017)
- Year:
- 2017
- Volume:
- 66
- Issue:
- 10
- Issue Sort Value:
- 2017-0066-0010-0000
- Page Start:
- 1829
- Page End:
- 1837
- Publication Date:
- 2016-04-21
- Subjects:
- HEPATITIS C -- CELLULAR IMMUNITY -- GENETIC POLYMORPHISMS -- IMMUNOLOGY -- MOLECULAR GENETICS
Gastroenterology -- Periodicals
616.33 - Journal URLs:
- http://gut.bmjjournals.com ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/gutjnl-2015-310239 ↗
- Languages:
- English
- ISSNs:
- 0017-5749
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 18576.xml