Polymorphisms in melanoma differentiation‐associated gene 5 link protein function to clearance of hepatitis C virus. Issue 2 (5th January 2015)
- Record Type:
- Journal Article
- Title:
- Polymorphisms in melanoma differentiation‐associated gene 5 link protein function to clearance of hepatitis C virus. Issue 2 (5th January 2015)
- Main Title:
- Polymorphisms in melanoma differentiation‐associated gene 5 link protein function to clearance of hepatitis C virus
- Authors:
- Hoffmann, Franziska S.
Schmidt, Andreas
Dittmann Chevillotte, Meike
Wisskirchen, Christian
Hellmuth, Johannes
Willms, Simone
Gilmore, Rachel H.
Glas, Jürgen
Folwaczny, Matthias
Müller, Tobias
Berg, Thomas
Spengler, Ulrich
Fitzmaurice, Karen
Kelleher, Dermot
Reisch, Nicole
Rice, Charles M.
Endres, Stefan
Rothenfusser, Simon - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="hep27344-sec-0001" sec-type="section"> <p>Among patients newly infected with hepatitis C virus (HCV), only 20‐30% clear the infection spontaneously. In the remaining 70% the infection persists, causing chronic liver inflammation and disease. It is well established that polymorphisms in host genes, especially in components of the innate immune response, contribute to the phenomenon of spontaneous HCV clearance. Retinoic acid inducible gene‐I (RIG‐I)‐like helicases such as melanoma differentiation‐associated gene 5 (MDA‐5) are cytoplasmic sensors of viral RNA that are critical for triggering innate immune responses after infection with RNA viruses. We analyzed 14 nonsynonymous single‐nucleotide polymorphisms in RIG‐I‐like helicase‐pathway‐genes comparing European patients who spontaneously cleared HCV (n = 285) or had persistent infection (n = 509). We found that polymorphic haplotypes in the MDA‐5 gene <italic>IFIH1</italic> encoding histidine at position 843 and threonine at position 946 strongly correlate with the resolution of HCV infection (odds ratio [OR]: 16.23; 95% confidence interval [CI]: 3.67‐71.87; <italic>P</italic> = 1.1 × 10<sup>−6</sup>). Overexpression of MDA‐5 genetic variants in HEK 293 cells and in a tissue culture model of HCV infection revealed that the histidine 843/threonine 946 variant leads to increased baseline and ligand‐induced expression of<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="hep27344-sec-0001" sec-type="section"> <p>Among patients newly infected with hepatitis C virus (HCV), only 20‐30% clear the infection spontaneously. In the remaining 70% the infection persists, causing chronic liver inflammation and disease. It is well established that polymorphisms in host genes, especially in components of the innate immune response, contribute to the phenomenon of spontaneous HCV clearance. Retinoic acid inducible gene‐I (RIG‐I)‐like helicases such as melanoma differentiation‐associated gene 5 (MDA‐5) are cytoplasmic sensors of viral RNA that are critical for triggering innate immune responses after infection with RNA viruses. We analyzed 14 nonsynonymous single‐nucleotide polymorphisms in RIG‐I‐like helicase‐pathway‐genes comparing European patients who spontaneously cleared HCV (n = 285) or had persistent infection (n = 509). We found that polymorphic haplotypes in the MDA‐5 gene <italic>IFIH1</italic> encoding histidine at position 843 and threonine at position 946 strongly correlate with the resolution of HCV infection (odds ratio [OR]: 16.23; 95% confidence interval [CI]: 3.67‐71.87; <italic>P</italic> = 1.1 × 10<sup>−6</sup>). Overexpression of MDA‐5 genetic variants in HEK 293 cells and in a tissue culture model of HCV infection revealed that the histidine 843/threonine 946 variant leads to increased baseline and ligand‐induced expression of interferon‐induced genes and confers an increased ability to suppress HCV replication. <italic>Conclusion</italic>: These data suggest that MDA‐5 plays a significant role in the defense against HCV and that polymorphisms in MDA‐5 can influence the outcome of HCV infection. (H<sc>epatology</sc> 2015;61:460‐470)</p> </sec> </abstract> … (more)
- Is Part Of:
- Hepatology. Volume 61:Issue 2(2015:Feb.)
- Journal:
- Hepatology
- Issue:
- Volume 61:Issue 2(2015:Feb.)
- Issue Display:
- Volume 61, Issue 2 (2015)
- Year:
- 2015
- Volume:
- 61
- Issue:
- 2
- Issue Sort Value:
- 2015-0061-0002-0000
- Page Start:
- 460
- Page End:
- 470
- Publication Date:
- 2015-01-05
- Subjects:
- Heart -- Diseases -- Nursing -- Periodicals
Lungs -- Diseases -- Nursing -- Periodicals
Intensive care nursing -- Periodicals
Foie -- Maladies -- Périodiques
616.362 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1527-3350 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/hep.27344 ↗
- Languages:
- English
- ISSNs:
- 0270-9139
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4295.836000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3895.xml