Polymorphism of programmed death-1 (PD-1) gene in relation to susceptibility and progression of hepatitis B virus infection in Egyptian patients | ||||
Egyptian Journal of Medical Microbiology | ||||
Volume 29, Issue 2, April 2020, Page 55-62 PDF (430.41 K) | ||||
Document Type: New and original researches in the field of Microbiology. | ||||
DOI: 10.21608/ejmm.2020.250018 | ||||
View on SCiNiTO | ||||
Authors | ||||
Samah M. Awad* 1; Hanaa M. El Gazzar1; Naglaa Allam2; Osama Elbahr2; Azza M. Abd El Aziz1 | ||||
1Department of Clinical Microbiology and Immunology and Molecular Microbiology in liver and Gastrointestinal Tract, National Liver Institute, Menoufia University, Menoufia, Egypt | ||||
2Depatment of Hepatology and Gastroenterology, National Liver Institute, Menoufia University, Menoufia, Egypt | ||||
Abstract | ||||
Background: chronic infection with hepatitis B virus (HBV) is a major risk factor for liver cirrhosis and hepatocellular carcinoma (HCC). Programmed death-1 (PD-1) has been involved in regulating immune responses to viral infections and tumors and has a critical role in HBV infection. Objectives: to investigate the effect of PD1 (+8669 G/A) single-nucleotide polymorphism (SNP) on disease susceptibility and progression of chronic HBV infection in Egyptian patients. Methodology: Blood samples were taken from 70 patients with confirmed chronic hepatitis B (CHB), HBV-related liver cirrhosis (LC) or HCC on top of HBV infection and 25 healthy controls. Genotyping of PD1 (+8669 G/A) polymorphism was studied using bidirectional PCR amplification of specific alleles (Bi-PASA). Results: A significantly higher frequency of PD-1 (+8669 G/A) AA genotype and A allele was found in CHB group (36.8 %) and LC group (21.7%) compared to control group (0.0%) (P< 0.05). On the other hand, the GG genotype and G allele were over represented in healthy controls (72.7%) than CHB group (52.6%) and LC group (47.8%). In assessing the risk of susceptibility to infection with HBV, The G allele was significantly predominant in healthy subjects compared to hepatitis B patients (89.4% versus 68.5%) (P< 0.05). G allele was markedly increased with disease progression to HCC (P = 0.006). Conclusion: Our study suggested that PD1 (+8669) polymorphism has significantly implicated in the disease susceptibility with AA genotype and A allele as a predisposing and the GG genotype and G allele as a preventive factors for chronic HBV infection. Also this study revealed a significant effect of the PD1 (+8669) polymorphism in the progression to HCC in hepatitis B patients. | ||||
Keywords | ||||
PD-1polymorphism; HBV; HCC | ||||
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