The interferon signaling pathway genes as biomarkers of hepatitis C virus disease progression and response to treatment

被引:4
作者
Helbig, Karla J. [1 ]
Beard, Michael R. [1 ]
机构
[1] Univ Adelaide, Sch Mol & Biomed Sci, Adelaide, SA 5000, Australia
关键词
biomarker; CXCL10; hepatitis C virus; IL28B; interferon; polymorphism; SINGLE NUCLEOTIDE POLYMORPHISM; PEGYLATED INTERFERON; RIBAVIRIN THERAPY; PLUS RIBAVIRIN; NATURAL-HISTORY; IFN-LAMBDA; INFECTION; EXPRESSION; HCV; ASSOCIATION;
D O I
10.2217/BMM.12.9
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Hepatitis C virus is an ever-increasing worldwide health problem with over 350,000 individuals succumbing to hepatitis C virus-related liver diseases each year. The ability to determine the outcome of an acute-phase illness may be useful in terms of implementing treatment strategies; however, to date, the predictive associations in the literature have centered around candidate gene analysis. Much greater advancements have been made in describing biomarkers from the activation of the host innate immune response, such as the interferon system, for prediction of treatment outcome in chronic hepatitis C with the advent of genome-wide association studies. Recent times has seen a major breakthrough in the field with the description of the IL28B genotype as an independent association factor for pegylated IFN-alpha 2b/ribavirin treatment response. The ability to couple this with other easily measured biomarkers such as the interferon-stimulated gene CXCL10, serum concentration may make this predictive marker set very useful in the clinical setting.
引用
收藏
页码:141 / 150
页数:10
相关论文
共 73 条
[11]   Quantitation of Pretreatment Serum Interferon-γ-Inducible Protein-10 Improves the Predictive Value of an IL28B Gene Polymorphism for Hepatitis C Treatment Response [J].
Darling, Jama M. ;
Aerssens, Jeroen ;
Fanning, Gregory ;
McHutchison, John G. ;
Goldstein, David B. ;
Thompson, Alexander J. ;
Shianna, Kevin V. ;
Afdhal, Nezam H. ;
Hudson, Michael L. ;
Howell, Charles D. ;
Talloen, Willem ;
Bollekens, Jacques ;
De Wit, Mieke ;
Scholliers, Annick ;
Fried, Michael W. .
HEPATOLOGY, 2011, 53 (01) :14-22
[12]   Association of pretreatment serum interferon γ inducible protein 10 levels with sustained virological response to peginterferon plus ribavirin therapy in genotype 1 infected patients with chronic hepatitis C [J].
Diago, M ;
Castellano, G ;
García-Samaniego, J ;
Pérez, C ;
Fernández, I ;
Romero, M ;
Iacono, OL ;
García-Monzón, C .
GUT, 2006, 55 (03) :374-379
[13]   Interferon-Induced Gene Expression Is a Stronger Predictor of Treatment Response Than IL28B Genotype in Patients With Hepatitis C [J].
Dill, Michael T. ;
Duong, Francois H. T. ;
Vogt, Julia E. ;
Bibert, Stephanie ;
Bochud, Pierre-Yves ;
Terracciano, Luigi ;
Papassotiropoulos, Andreas ;
Roth, Volker ;
Heim, Markus H. .
GASTROENTEROLOGY, 2011, 140 (03) :1021-U471
[14]   Single nucleotide polymorphism at exon 7 splice acceptor site of OAS1 gene determines response of hepatitis C virus patients to interferon therapy [J].
El Awady, Mostafa K. ;
Anany, Mohamed A. ;
Esmat, Gamal ;
Zayed, Naglaa ;
Tabll, Ashraf A. ;
Helmy, Amr ;
El Zayady, Abdel Rahman ;
Abdalla, Mohga S. ;
Sharada, Hayat M. ;
El Raziky, Maissa ;
El Akel, Wafaa ;
Abdalla, Shadia ;
El Din, Noha G. Bader .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2011, 26 (05) :843-850
[15]   Interferon-α inhibits hepatitis C virus subgenomic RNA replication by an MxA-independent pathway [J].
Frese, M ;
Pietschmann, T ;
Moradpour, D ;
Haller, O ;
Bartenschlager, R .
JOURNAL OF GENERAL VIROLOGY, 2001, 82 :723-733
[16]   Peginterferon alfa-2a plus ribavirin for chronic hepatitis C virus infection. [J].
Fried, MW ;
Shiffman, ML ;
Reddy, KR ;
Smith, C ;
Marinos, G ;
Goncales, FL ;
Haussinger, D ;
Diago, M ;
Carosi, G ;
Dhumeaux, D ;
Craxi, A ;
Lin, A ;
Hoffman, J ;
Yu, J .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (13) :975-982
[17]   Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance [J].
Ge, Dongliang ;
Fellay, Jacques ;
Thompson, Alexander J. ;
Simon, Jason S. ;
Shianna, Kevin V. ;
Urban, Thomas J. ;
Heinzen, Erin L. ;
Qiu, Ping ;
Bertelsen, Arthur H. ;
Muir, Andrew J. ;
Sulkowski, Mark ;
McHutchison, John G. ;
Goldstein, David B. .
NATURE, 2009, 461 (7262) :399-401
[18]   Potential Role for Interleukin-28B Genotype in Treatment Decision-Making in Recent Hepatitis C Virus Infection [J].
Grebely, Jason ;
Petoumenos, Kathy ;
Hellard, Margaret ;
Matthews, Gail V. ;
Suppiah, Vijayaprakash ;
Applegate, Tanya ;
Yeung, Barbara ;
Marks, Phillipa ;
Rawlinson, William ;
Lloyd, Andrew R. ;
Booth, David ;
Kaldor, John M. ;
George, Jacob ;
Dore, Gregory J. .
HEPATOLOGY, 2010, 52 (04) :1216-1224
[19]   Global transcriptional response to interferon is a determinant of HCV treatment outcome and is modified by race [J].
He, Xiao-Song ;
Ji, Xuhuai ;
Hale, Matthew B. ;
Cheung, Ramsey ;
Ahmed, Aijaz ;
Guo, Yaqian ;
Nolan, Garry P. ;
Pfeffer, Lawrence M. ;
Wright, Teresa L. ;
Risch, Neil ;
Tibshirani, Robert ;
Greenberg, Harry B. .
HEPATOLOGY, 2006, 44 (02) :352-359
[20]   Differential Expression of the CXCR3 Ligands in Chronic Hepatitis C Virus (HCV) Infection and Their Modulation by HCV In Vitro [J].
Helbig, Karla J. ;
Ruszkiewicz, Andrew ;
Lanford, Robert E. ;
Berzsenyi, Mark D. ;
Harley, Hugh A. ;
McColl, Shaun R. ;
Beard, Michael R. .
JOURNAL OF VIROLOGY, 2009, 83 (02) :836-846