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Interleukin-28B polymorphisms are associated with histological recurrence and treatment response following liver transplantation in patients with hepatitis C virus infection.

Publication ,  Journal Article
Charlton, MR; Thompson, A; Veldt, BJ; Watt, K; Tillmann, H; Poterucha, JJ; Heimbach, JK; Goldstein, D; McHutchison, J
Published in: Hepatology
January 2011

UNLABELLED: Polymorphism in the interleukin-28B (IL28B) gene region, encoding interferon (IFN)-λ3, is strongly predictive of response to antiviral treatment in the nontransplant setting. We sought to determine the prevalence and impact on clinical outcomes of donor and recipient IL28B genotypes among liver transplant recipients. The cohort study included 189 consecutive patients infected with hepatitis C virus (HCV) who underwent liver transplantation between January 1, 1995, and January 1, 2005, at the Mayo Clinic, Rochester, MN. Genotyping of the polymorphism rs12979860 was performed on DNA collected from all donors and recipients in the cohort. Sixty-five patients received IFN-based antiviral therapy. The CC IL28B variant was less common in the chronic HCV-infected recipients than in non-HCV donor livers (33% versus 47%, P = 0.03). IL28B recipient genotype was significantly predictive of fibrosis stage, with TT genotype being associated with more rapid fibrosis (Pearson chi-square P = 0.024 for the comparison G versus A). Donor and recipient IL28B genotype were independently associated with sustained virologic response (P < 0.005). The presence of IL28B CC variant in either the recipient (R) or donor (D) liver was associated with increased rate of sustained virologic response (D-non-CC/R-non-CC = 3/19 [16%] versus D-CC/R-non-CC = 11/22 [50%] versus D-non-CC/R-CC = 5/12 [42%] versus R-CC/D-CC = 6/7 [86%], P = 0.0095). IL28B genotype was not significantly associated with survival (overall/liver-related). CONCLUSION: Recipient IL28B TT genotype is associated with more severe histological recurrence of HCV. Recipient and donor liver IL28B genotype are strongly and independently associated with IFN-based treatment response in patients after orthotopic liver transplantation. The data suggest that CC donor livers might be preferentially allocated to patients with HCV infection.

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Published In

Hepatology

DOI

EISSN

1527-3350

Publication Date

January 2011

Volume

53

Issue

1

Start / End Page

317 / 324

Location

United States

Related Subject Headings

  • Retrospective Studies
  • Polymorphism, Single Nucleotide
  • Middle Aged
  • Male
  • Liver Transplantation
  • Interleukins
  • Interferons
  • Humans
  • Hepatitis C, Chronic
  • Gastroenterology & Hepatology
 

Citation

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MLA
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Charlton, M. R., Thompson, A., Veldt, B. J., Watt, K., Tillmann, H., Poterucha, J. J., … McHutchison, J. (2011). Interleukin-28B polymorphisms are associated with histological recurrence and treatment response following liver transplantation in patients with hepatitis C virus infection. Hepatology, 53(1), 317–324. https://doi.org/10.1002/hep.24074
Charlton, Michael R., Alexander Thompson, Bart J. Veldt, Kym Watt, Hans Tillmann, John J. Poterucha, Julie K. Heimbach, David Goldstein, and John McHutchison. “Interleukin-28B polymorphisms are associated with histological recurrence and treatment response following liver transplantation in patients with hepatitis C virus infection.Hepatology 53, no. 1 (January 2011): 317–24. https://doi.org/10.1002/hep.24074.
Charlton, Michael R., et al. “Interleukin-28B polymorphisms are associated with histological recurrence and treatment response following liver transplantation in patients with hepatitis C virus infection.Hepatology, vol. 53, no. 1, Jan. 2011, pp. 317–24. Pubmed, doi:10.1002/hep.24074.
Charlton MR, Thompson A, Veldt BJ, Watt K, Tillmann H, Poterucha JJ, Heimbach JK, Goldstein D, McHutchison J. Interleukin-28B polymorphisms are associated with histological recurrence and treatment response following liver transplantation in patients with hepatitis C virus infection. Hepatology. 2011 Jan;53(1):317–324.
Journal cover image

Published In

Hepatology

DOI

EISSN

1527-3350

Publication Date

January 2011

Volume

53

Issue

1

Start / End Page

317 / 324

Location

United States

Related Subject Headings

  • Retrospective Studies
  • Polymorphism, Single Nucleotide
  • Middle Aged
  • Male
  • Liver Transplantation
  • Interleukins
  • Interferons
  • Humans
  • Hepatitis C, Chronic
  • Gastroenterology & Hepatology