{"title":"Factors Affecting the Response to Interferon Alpha Therapy in Egyptian HCV Patients","authors":"N. Alhusseini, F. Serry, A. A. Kadry, H. Khairy","doi":"10.3844/AJISP.2015.92.101","DOIUrl":null,"url":null,"abstract":"Hepatitis C Virus (HCV) infection is one of the main causes of chronic liver disease worldwide. Egypt has the highest prevalence of Hepatitis C Virus (HCV) in the world, estimated nationally at 14.7%. knowledge of the predictors of Sustained Viral Response (SVR) to Pegylated Interferon (PEG-INF) and Ribavirin (RBV) therapy in patients with chronic hepatitis C is crucial for selecting patients who would benefit most from therapy especially in developing country as Egypt where the highest percentage of treatment cost funded by government. This study was performed on Egyptian patients with chronic active hepatitis C who were prepared for receiving a course of treatment with: Interferon (PEG IFN) and ribavirin for 48 weeks. We aimed to find more predictive markers those can help clinicians to choose the most effective treatment program for each patient. Assessment of HLA-DRB1, HLA-DQB1 genes by Sequence Specific Primer (SSP) PCR, interleukin-10 (IL-10) by ELISA technique and Serum HCV RNA load by TaqMan Real Time RT-PCR technology were done. We found that sustained responders were significantly among DRB1*13 allele and DQB1*02 typing (p<0.001). DRB1*07 allele only appeared with responded patients. Relations were found between response to treatment and lower IL-10 level and lower Body Mass Index (BMI) but not sufficient to reach to significant value. In conclusion, we emphasize the importance of the use of pharmacogenomic data in the treatment of patients. HLA-DRB1*07, HLA-DRB1*13 and HLA-DQ02 alleles can predict the response to HCV combined therapy. The data generated from our study may be helpful in future for clinicians to predict the treatment outcome for HCV-seropositive individuals in Egypt.","PeriodicalId":88361,"journal":{"name":"American journal of immunology","volume":"11 1","pages":"92-101"},"PeriodicalIF":0.0000,"publicationDate":"2015-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3844/AJISP.2015.92.101","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of immunology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3844/AJISP.2015.92.101","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Hepatitis C Virus (HCV) infection is one of the main causes of chronic liver disease worldwide. Egypt has the highest prevalence of Hepatitis C Virus (HCV) in the world, estimated nationally at 14.7%. knowledge of the predictors of Sustained Viral Response (SVR) to Pegylated Interferon (PEG-INF) and Ribavirin (RBV) therapy in patients with chronic hepatitis C is crucial for selecting patients who would benefit most from therapy especially in developing country as Egypt where the highest percentage of treatment cost funded by government. This study was performed on Egyptian patients with chronic active hepatitis C who were prepared for receiving a course of treatment with: Interferon (PEG IFN) and ribavirin for 48 weeks. We aimed to find more predictive markers those can help clinicians to choose the most effective treatment program for each patient. Assessment of HLA-DRB1, HLA-DQB1 genes by Sequence Specific Primer (SSP) PCR, interleukin-10 (IL-10) by ELISA technique and Serum HCV RNA load by TaqMan Real Time RT-PCR technology were done. We found that sustained responders were significantly among DRB1*13 allele and DQB1*02 typing (p<0.001). DRB1*07 allele only appeared with responded patients. Relations were found between response to treatment and lower IL-10 level and lower Body Mass Index (BMI) but not sufficient to reach to significant value. In conclusion, we emphasize the importance of the use of pharmacogenomic data in the treatment of patients. HLA-DRB1*07, HLA-DRB1*13 and HLA-DQ02 alleles can predict the response to HCV combined therapy. The data generated from our study may be helpful in future for clinicians to predict the treatment outcome for HCV-seropositive individuals in Egypt.
丙型肝炎病毒(HCV)感染是全球慢性肝病的主要原因之一。埃及是世界上丙型肝炎病毒(HCV)流行率最高的国家,全国估计为14.7%。了解慢性丙型肝炎患者对聚乙二醇化干扰素(PEG-INF)和利巴韦林(RBV)治疗的持续病毒反应(SVR)预测因素对于选择从治疗中获益最多的患者至关重要,特别是在埃及这样的发展中国家,政府资助的治疗费用比例最高。这项研究是在埃及慢性活动性丙型肝炎患者中进行的,他们准备接受干扰素(PEG IFN)和利巴韦林48周的疗程治疗。我们的目标是找到更多的预测指标,这些指标可以帮助临床医生为每个患者选择最有效的治疗方案。采用序列特异性引物(SSP) PCR检测HLA-DRB1、HLA-DQB1基因,采用ELISA技术检测白细胞介素-10 (IL-10),采用TaqMan Real Time RT-PCR技术检测血清HCV RNA载量。我们发现持续应答者在DRB1*13等位基因和DQB1*02型中有显著性差异(p<0.001)。DRB1*07等位基因仅在有应答的患者中出现。治疗反应与降低IL-10水平和降低身体质量指数(BMI)之间存在相关性,但不足以达到显著值。总之,我们强调药物基因组学数据在患者治疗中的重要性。HLA-DRB1*07、HLA-DRB1*13和HLA-DQ02等位基因可以预测HCV联合治疗的疗效。从我们的研究中产生的数据可能有助于临床医生预测埃及hcv血清阳性个体的治疗结果。