Pretreatment serum levels of interferon-gamma-inducible protein-10 are associated with virologic response to telaprevir-based therapy

被引:1
作者
Yamagiwa, Yoko [1 ]
Asano, Mai [1 ]
Kawasaki, Youhei [2 ]
Korenaga, Masaaki [1 ]
Murata, Kazumoto [1 ]
Kanto, Tatsuya [1 ]
Mizokami, Masashi [1 ]
Masaki, Naohiko [1 ]
机构
[1] Natl Ctr Global Hlth & Med, Res Ctr Hepatitis & Immunol, 1-7-1 Konodai, Ichikawa, Chiba 2728516, Japan
[2] Univ Shizuoka, Grad Sch Pharmaceut Sci, Dept Drug Evaluat & Informat, Shizuoka, Shizuoka 4228526, Japan
关键词
Chronic hepatitis C; IL28B; IP-10; Rapid virologic response; Telaprevir; CHRONIC HEPATITIS-C; GENOME-WIDE ASSOCIATION; AMINO-ACID SUBSTITUTION; CHRONIC HCV INFECTION; GENOTYPE; INFECTION; VIRUS-INFECTION; GENETIC-VARIATION; VIRAL RESPONSE; PEGYLATED INTERFERON; COMBINATION THERAPY;
D O I
10.1016/j.cyto.2016.07.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aim: Telaprevir (TVR) remarkably improves the efficacy of interferon treatment for chronic hepatitis C. Interleukin-28B (IL28B) genotype and interferon-gamma-inducible protein-10 (IP-10) level predict virologic response to peg-interferon (Peg-IFN)/ribavirin (RBV) therapy. We aimed to investigate the usefulness of pretreatment serum IP-10 levels and IL28B genotyping in predicting sustained virologic response (SVR) to TVR-based triple therapy. Methods: In this multi-center study, patients infected with hepatitis C virus genotype 1 with high viral load ( >= 5.0 log IU/mL) were treated with TVR for 12 weeks. and Peg-IFN/RBV for 24 weeks in Japan. IL28B genotype, serum IP-10 levels, other clinical parameters, and drug dosages were assessed before treatment. Results: We included 121 patients who were treated with TVR for at least 8 weeks and Peg-IFN/RBV for 24 weeks. The median IP-10 levels were significantly lower in rapid virologic response (RVR) or SVR in the IL28B non-TT genotype group, with no significant difference in the TT genotype group. RVR rates were significantly lower in the group with higher serum IP-10 levels (>450 pg/mL). In the non-TT IL28B genotype group, RVR and SVR rates were significantly lower in the group with higher IP-10 levels. SVR rates in the group with lower IP-10 levels (<450 pg/mL) increased to 82% for those showing RVR, but reduced to 27% in the group with higher IP-10 levels for those not showing RVR. Conclusions: Determination of serum IP-10 levels before treatment could be useful for predicting favorable virologic response to TVR-based triple therapy, especially in patients with IL28B non-TT genotype. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:29 / 36
页数:8
相关论文
共 43 条
[1]   Association of amino acid substitution pattern in core protein of hepatitis C virus genotype 1b high viral load and non-virological response to interferon-ribavirin combination therapy [J].
Akuta, N ;
Suzuki, F ;
Sezaki, H ;
Suzuki, Y ;
Hosaka, T ;
Someya, T ;
Kobayashi, M ;
Saitoh, S ;
Watahiki, S ;
Sato, J ;
Matsuda, M ;
Kobayashi, M ;
Arase, Y ;
Ikeda, K ;
Kumada, H .
INTERVIROLOGY, 2005, 48 (06) :372-380
[2]   Amino Acid Substitution in Hepatitis C Virus Core Region and Genetic Variation Near the Interleukin 28B Gene Predict Viral Response to Telaprevir with Peginterferon and Ribavirin [J].
Akuta, Norio ;
Suzuki, Fumitaka ;
Hirakawa, Miharu ;
Kawamura, Yusuke ;
Yatsuji, Hiromi ;
Sezaki, Hitomi ;
Suzuki, Yoshiyuki ;
Hosaka, Tetsuya ;
Kobayashi, Masahiro ;
Kobayashi, Mariko ;
Saitoh, Satoshi ;
Arase, Yasuji ;
Ikeda, Kenji ;
Chayama, Kazuaki ;
Nakamura, Yusuke ;
Kumada, Hiromitsu .
HEPATOLOGY, 2010, 52 (02) :421-429
[3]   Chemokine (C-X-C motif) ligand (CXCL)10 in autoimmune diseases [J].
Antonelli, Alessandro ;
Ferrari, Silvia Martina ;
Giuggioli, Dilia ;
Ferrannini, Ele ;
Ferri, Clodoveo ;
Fallahi, Poupak .
AUTOIMMUNITY REVIEWS, 2014, 13 (03) :272-280
[4]   Association of gene expression involving innate immunity and genetic variation in interleukin 28B with antiviral response [J].
Asahina, Yasuhiro ;
Tsuchiya, Kaoru ;
Muraoka, Masaru ;
Tanaka, Keisuke ;
Suzuki, Yuichiro ;
Tamaki, Nobuharu ;
Hoshioka, Yoshihide ;
Yasui, Yutaka ;
Katoh, Tomoji ;
Hosokawa, Takanori ;
Ueda, Ken ;
Nakanishi, Hiroyuki ;
Itakura, Jun ;
Takahashi, Yuka ;
Kurosaki, Masayuki ;
Enomoto, Nobuyuki ;
Nitta, Sayuri ;
Sakamoto, Naoya ;
Izumi, Namiki .
HEPATOLOGY, 2012, 55 (01) :20-29
[5]   Systemic and Intrahepatic Interferon-Gamma-Inducible Protein 10 kDa Predicts the First-Phase Decline in Hepatitis C Virus RNA and Overall Viral Response to Therapy in Chronic Hepatitis C [J].
Askarieh, Galia ;
Alsio, Asa ;
Pugnale, Paolo ;
Negro, Francesco ;
Ferrari, Carlo ;
Neumann, Avidan U. ;
Pawlotsky, Jean-Michel ;
Schalm, Solko W. ;
Zeuzem, Stefan ;
Norkrans, Gunnar ;
Westin, Johan ;
Soderholm, Jonas ;
Hellstrand, Kristoffer ;
Lagging, Martin .
HEPATOLOGY, 2010, 51 (05) :1523-1530
[6]   Plasma chemokine levels correlate with the outcome of antiviral therapy in patients with hepatitis C [J].
Butera, D ;
Marukian, S ;
Iwamaye, AE ;
Hembrador, E ;
Chambers, TJ ;
Di Bisceglie, AM ;
Charles, ED ;
Talal, AH ;
Jacobson, IM ;
Rice, CM ;
Dustin, LB .
BLOOD, 2005, 106 (04) :1175-1182
[7]   IL28B But Not ITPA Polymorphism Is Predictive of Response to Pegylated Interferon, Ribavirin, and Telaprevir Triple Therapy in Patients With Genotype 1 Hepatitis C [J].
Chayama, Kazuaki ;
Hayes, C. Nelson ;
Abe, Hiromi ;
Miki, Daiki ;
Ochi, Hidenori ;
Karino, Yoshiyasu ;
Toyota, Joji ;
Nakamura, Yusuke ;
Kamatani, Naoyuki ;
Sezaki, Hitomi ;
Kobayashi, Mariko ;
Akuta, Norio ;
Suzuki, Fumitaka ;
Kumada, Hiromitsu .
JOURNAL OF INFECTIOUS DISEASES, 2011, 204 (01) :84-93
[8]   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
[9]   Genomics and HCV infection: Progression of fibrosis and treatment response [J].
Estrabaud, Emilie ;
Vidaud, Michel ;
Marcellin, Patrick ;
Asselah, Tarik .
JOURNAL OF HEPATOLOGY, 2012, 57 (05) :1110-1125
[10]   Hepatic gene expression during treatment with peginterferon and ribavirin: Identifying molecular pathways for treatment response [J].
Feld, Jordan J. ;
Nanda, Santosh ;
Huang, Ying ;
Chen, Weiping ;
Cam, Maggie ;
Pusek, Susan N. ;
Schweigler, Lisa M. ;
Theodore, Dickens ;
Zacks, Steven L. ;
Liang, T. Jake ;
Fried, Michael W. .
HEPATOLOGY, 2007, 46 (05) :1548-1563