Interleukin 28B Genetic Polymorphisms Play a Minor Role in Identifying Optimal Treatment Duration in HCV Genotype 1 Slow Responders to Pegylated Interferon plus Ribavirin
Author(s) -
ChenHua Liu,
ChengChao Liang,
ChunJen Liu,
TaiChung Tseng,
ChihLin Lin,
ShengShun Yang,
TungHung Su,
JouWei Lin,
Jun-Herng Chen,
PeiJer Chen,
DingShinn Chen,
JiaHorng Kao
Publication year - 2012
Publication title -
antiviral therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.747
H-Index - 87
eISSN - 2040-2058
pISSN - 1359-6535
DOI - 10.3851/imp2322
Subject(s) - ribavirin , pegylated interferon , medicine , interleukin 28b , viral load , gastroenterology , genotype , snp , hepatitis c virus , immunology , single nucleotide polymorphism , biology , virus , biochemistry , gene
Pegylated interferon and ribavirin for 72 weeks improve sustained virological response (SVR) in HCV genotype 1 (HCV-1) slow viral responders. Whether interleukin 28B (IL28B) single nucleotide polymorphism (SNP) genotypes and on-treatment viral responses can identify non-rapid virological response (RVR) patients who benefit from 48 or 72 weeks of therapy remains unclear.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom