Impact of HCV Genome Structure on Responder to Pegylated Interferon Therapy in Egyptian Patients

被引:0
作者
Abdallah, Sanaa Osama [1 ]
El-Dessouky, Mohamed Ali [1 ]
Hassanein, Moataz Hassan [2 ]
Omar, Hanan [3 ]
El Sehrawy, Khaled Mohamed Farid [1 ]
机构
[1] Cairo Univ, Fac Sci, Chem Dept, Giza, Egypt
[2] Theodor Bilharz Res Inst, Hepatol & Gastroenterol Dept, Giza, Egypt
[3] Theodor Bilharz Res Inst, Biochem & Mol Biol Dept, Giza, Egypt
来源
INTERNATIONAL JOURNAL OF PHARMACEUTICAL RESEARCH AND ALLIED SCIENCES | 2019年 / 8卷 / 03期
关键词
Hepatitis C virus; Pegylated Interferon-alpha; IRES; ISDR; HEPATITIS-C VIRUS; SENSITIVITY-DETERMINING REGION; RIBAVIRIN COMBINATION THERAPY; RIBOSOME ENTRY SITE; PLUS RIBAVIRIN; 5A GENE; MUTATIONS; VARIABILITY; RESISTANCE; 1B;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study aimed to investigate relationship of the HCV genome structure and treatment with Pegylated Inteiferon-alpha/Ribavirin (peg-IFN alpha/RBT) Egyptian patient. Mutations in two sites of HCV genome; the internal ribosome entry site (IRES) and the interferon sensitivity determining region (ISDR) of HCV genotype 4 alpha were studied in details including DNA sequences and mutations detection in response to treatment. Ninety patients, responders and non-responders, to treatment with peg-IFN alpha/RBV were included in this study. IRES and ISDR regions were amplified by RT-PCR using specific designed primers, and amplified regions were sequenced. The data obtained were aligned with published sequences in GenBank using BLAST program. Results of this study have revealed that there are different mutations in the studied sequences in both ISDR and IRES regions. The predicted amino acids sequences in the ISDR region showed significant differences ranging from one up to more than eight mutations in the HCV Genome sequences. Although there was a significant difference between sequences of HCV RNA isolated from responders and non-responders, these data were not able to give an absolute answer whether response to interferon therapy is directly/relates to the structure of the HCV genome.
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页码:61 / 68
页数:8
相关论文
共 31 条
[1]   Optimal therapy in genotype 4 chronic hepatitis C: finally cured? [J].
Abdel-Razek, Wael ;
Waked, Imam .
LIVER INTERNATIONAL, 2015, 35 :27-34
[2]   Natural history of hepatitis C [J].
Alberti, A ;
Chemello, L ;
Benvegnù, L .
JOURNAL OF HEPATOLOGY, 1999, 31 :17-24
[3]   Peginterferon Alfa-2a Plus Ribavirin Is More Effective Than Peginterferon Alfa-2b Plus Ribavirin for Treating Chronic Hepatitis C Virus Infection [J].
Ascione, Antonio ;
De Luca, Massimo ;
Tartaglione, Maria Teresa ;
Lampasi, Filippo ;
Di Costanzo, Giovan Giuseppe ;
Lanza, Alfonso Galeota ;
Picciotto, Francesco Paolo ;
Marino-Marsilia, Giuseppina ;
Fontanella, Luca ;
Leandro, Gioacchino .
GASTROENTEROLOGY, 2010, 138 (01) :116-122
[4]   Analysis of Genotype 1b Hepatitis C Virus IRES in Serum and Peripheral Blood Mononuclear Cells in Patients Treated with Interferon and Ribavirin [J].
Bukowska-Osko, Iwona ;
Cortes, Kamila Caraballo ;
Pawelczyk, Agnieszka ;
Ploski, Rafal ;
Fic, Maria ;
Perlejewski, Karol ;
Demkow, Urszula ;
Berak, Hanna ;
Horban, Andrzej ;
Laskus, Tomasz ;
Radkowski, Marek .
BIOMED RESEARCH INTERNATIONAL, 2014, 2014
[5]   The role of surface basic amino acids of dengue virus NS3 helicase in viral RNA replication and enzyme activities [J].
Chiang, Pao-Yin ;
Wu, Huey-Nan .
FEBS LETTERS, 2016, 590 (14) :2307-2320
[6]   NS5A Sequence Heterogeneity of Hepatitis C Virus Genotype 4a Predicts Clinical Outcome of Pegylated-Interferon-Ribavirin Therapy in Egyptian Patients [J].
El-Shamy, Ahmed ;
Shoji, Ikuo ;
El-Akel, Wafaa ;
Bilasy, Shymaa E. ;
Deng, Lin ;
El-Raziky, Maissa ;
Jiang, Da-peng ;
Esmat, Gamal ;
Hotta, Hak .
JOURNAL OF CLINICAL MICROBIOLOGY, 2012, 50 (12) :3886-3892
[7]   Genetic Variability of Hepatitis C Virus in South Egypt and Its Possible Clinical Implication [J].
Elkady, Abeer ;
Tanaka, Yasuhito ;
Kurbanov, Fuat ;
Sugauchi, Fuminaka ;
Sugiyama, Masaya ;
Khan, Anis ;
Sayed, Douaa ;
Moustafa, Ghada ;
AbdEl-Hameed, AbdEl-Rahman ;
Mizokami, Masashi .
JOURNAL OF MEDICAL VIROLOGY, 2009, 81 (06) :1015-1023
[8]   Mutations in the nonstructural protein 5A gene and response to interferon in patients with chronic hepatitis C virus 1b infection [J].
Enomoto, N ;
Sakuma, I ;
Asahina, Y ;
Kurosaki, M ;
Murakami, T ;
Yamamoto, C ;
Ogura, Y ;
Izumi, N ;
Marumo, F ;
Sato, C .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (02) :77-81
[9]   Evidence that hepatitis C virus resistance to interferon is mediated through repression of the PKR protein kinase by the nonstructural 5A protein [J].
Gale, MJ ;
Korth, MJ ;
Tang, NM ;
Tan, SL ;
Hopkins, DA ;
Dever, TE ;
Polyak, SJ ;
Gretch, DR ;
Katze, MG .
VIROLOGY, 1997, 230 (02) :217-227
[10]   Two PKR inhibitor HCV proteins correlate with early but not sustained response to interferon [J].
Gerotto, M ;
Dal Pero, F ;
Pontisso, P ;
Noventa, F ;
Gatta, A ;
Alberti, A .
GASTROENTEROLOGY, 2000, 119 (06) :1649-1655