IL28B polymorphism -- predictive factor of HCV infected genotype 1 individuals to treatment response and management of therapy
Related Experiment Video
Updated: May 25, 2026

Analysis of HBV-Specific CD4 T-cell Responses and Identification of HLA-DR-Restricted CD4 T-Cell Epitopes Based on a Peptide Matrix
Published on: October 20, 2021
Florentina Ioniţă-Radu1, Aida Raşcanu, Bianca Cheiab
1"Dr. Carol Davila" Central Universitary Emergency Military Hospital, Bucharest, Romania. fionita04@yahoo.com
Insights
Identifying interleukin-28B (IL-28B) gene variations is crucial for predicting Hepatitis C Virus (HCV) treatment success. Personalized medicine approaches using IL-28B genotyping can improve sustained virological response (SVR) rates and reduce costs.
Area of Science:
- Hepatology
- Genetics
- Pharmacogenomics
Background:
- Chronic Hepatitis C Virus (HCV) infection affects 3% of the global population, with limited treatment efficacy.
- Standard therapy (PegIFN and ribavirin) yields only 40-50% sustained virological response (SVR) in genotype 1 patients.
- New triple therapies offer improved outcomes but raise concerns about cost and accessibility.
Purpose of the Study:
- To investigate host genetic factors, specifically IL-28B gene polymorphisms, as predictors of treatment response in HCV.
- To explore the role of IL-28B variations in achieving SVR with both standard and novel triple therapies.
- To emphasize the importance of personalized treatment strategies based on IL-28B genotyping.
Main Methods:
- Review of recent studies, including Genome-Wide Association Studies (GWAS).
- Focus on host polymorphisms upstream of the IL-28B gene.
- Analysis of treatment response data in relation to IL-28B genotypes.
Main Results:
- Host IL-28B gene polymorphisms are strongly associated with SVR to standard HCV therapy.
- IL-28B genotyping can help predict treatment outcomes for both standard and triple therapies.
- Personalized treatment selection based on IL-28B status can optimize SVR rates.
Conclusions:
- IL-28B gene polymorphism is a significant predictor of SVR in HCV treatment.
- Determining IL-28B genotype prior to treatment can guide therapy selection and improve outcomes.
- Personalized medicine incorporating IL-28B genotyping offers a cost-effective approach to enhance SVR and minimize adverse effects.
Abstract:
It is estimated that approximately 3% of the world population are chronically infected with HCV, as the annual incidence of HCV infection is approximately 3-4 million people. Despite all efforts made to eradicate the HCV infection, after the standard therapy (PegIFN and ribavirin for 48 weeks) only 40-50% of the HCV infected individuals with genotype 1 achieve sustained virological response (SVR). Since our goal today is the eradication of HCV infection, our prior concern has become the identification of predictor factors concerning treatment response. Recent studies such as GWAS have been concerned with the genetic factors and the response to treatment. Recently all interest has been turned towards the demonstration of the host polymorphism located upstream of the IL-28B gene and which is associated with sustained virological response to treatment with pegylated interferon Alfa in combination with ribavirin. Although 2011 comes with the FDA approval of the new triple therapy associating telaprevir/ boceprevir to the standard therapy, a new ethical concern regarding the high costs of this treatment rises the problem of who is the first in line? This is just the beginning of a new quest to further investigate the relationship between the host's polymorphism of the IL-28 gene and the standard and triple therapy in HCV infected individuals in achieving SVR as well as who should receive standard or triple therapy. Determination of the IL-28 polymorphisms may be used together with clinical assessment in order to evaluate patients and to personalize their treatment. The purpose of this paper is to underline the main concerns regarding the goal and endpoints of the HCV therapy, and the relationship of IL-28 in achieving sustained virological response, as well as in pointing out the importance to determine prior to initiating treatment the polymorphism of IL-28 since it is a strong predictor. This is important because it will increase the chances to achieve SVR, it will be cost-effective and reduces adverse effects.
Related Concept Videos
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Pharmacogenomics: Identification of New Drug Targets
Inhibitors of Viral Protein Synthesis
Pharmacogenetics of Phase II Enzymes: N-acetyltransferase, Thiopurine S-methyltransferase, UDP-glucuronosyltransferase

