Publications by authors named "Gui-zhen Zhao"

Aim: To build a hepatitis B virus (HBV)-infected human trophoblast cell model in vitro and determine the mechanism of intrauterine HBV infection.

Methods: Serum from hepatitis B-infected patients containing HBV DNA >10(9) was drawn, subsequently inoculated into human trophoblast cells in vitro (JEG3) and passage-cultured. The supernatants and intracellular HBV viral load of inoculated cells were tested by real-time PCR, and HBV DNA was determined by Southern blot.

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  • The study aimed to explore how serum levels of Th1/Th2 cytokines relate to the progression of viral hepatitis C and the effectiveness of interferon therapy.
  • Researchers used tests like ELISA and quantitative PCR to measure cytokines and HCV loads, finding that cytokine levels differed between chronic hepatitis C patients and healthy controls.
  • Results showed that while no cytokine levels correlated with interferon therapy outcomes before treatment, increased serum IFN-gamma after treatment was linked to better long-term responses.
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  • The study investigates how the hepatitis B virus (HBV) is passed from pregnant women to their fetuses, focusing on placental tissue and cultured cells.
  • Various laboratory techniques, including ELISA and RT-PCR, were used to examine placental samples from pregnant women with HBV.
  • Findings indicated a correlation between HBV levels in mothers and their babies; HBV was present in placental cells, suggesting that the virus can cross the placental barrier and potentially infect the fetus.
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  • The study aimed to explore the links between hepatitis C virus (HCV) genotype, viral load, ALT levels, and factors influencing viral relapse post-IFN treatment in chronic hepatitis C patients.
  • The research involved analyzing HCV RNA levels and genotypes in 208 patients treated with PEG-IFN alpha -2a and Roferon-A over a 24-week period, followed by a 24-week monitoring phase.
  • Results showed a high viral relapse rate of 48.7% among responders, with higher relapse rates in genotype 1 patients compared to non-genotype 1, suggesting that HCV genotype has a significant impact on the likelihood of relapse after treatment.
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  • The study aimed to assess the effectiveness of interferon (IFN) retreatment in chronic hepatitis C patients who relapsed after prior IFN therapy, focusing on various influencing factors.
  • Significant results indicated that PEG-IFNalpha-2a treatment led to higher end of treatment virus response (ETVR) and sustained viral response (SVR) rates compared to CIFNalpha-2a, particularly in patients with genotype 1.
  • Overall, while some patients did not respond to retreatment, PEG-IFNalpha-2a was found to be more effective than CIFNalpha-2a, with viral load having no impact on treatment response.
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  • This study investigates the factors that predict sustained viral response in chronic hepatitis C patients treated with two types of interferon: roferon-A and pegasys.
  • The research involved a randomized trial with assessments of HCV genotypes and RNA levels before and after a 24-week treatment, examining various clinical characteristics using logistic regression.
  • Results indicated that younger, female patients with specific infection routes and lower viral loads had better response rates, while those with higher AST/ALT ratios and viral loads showed greater sustained response post-treatment.
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  • The study aimed to identify predictors of response to interferon (IFN) therapy in chronic hepatitis C patients using multivariate logistic regression analysis.
  • Patients were randomly assigned to receive either pegasys or Roferon-A for 24 weeks, with their HCV RNA levels measured before, during, and after treatment.
  • The results indicated that while HCV genotype was not a predictor of immediate viral response, it was significant for sustained response, with pegasys and HCV genotype being key independent factors affecting treatment outcomes.
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  • The study evaluated how HCV genotype affects the response to interferon treatment in patients with chronic hepatitis C.
  • A total of 202 patients were analyzed, with a majority infected by genotype 1, who showed lower sustained viral response (SVR) rates compared to those with non-1 genotypes.
  • Results indicated that patients with genotype 1 had a higher likelihood of viral relapse and lower treatment effectiveness, suggesting that genotype significantly influences treatment success.
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  • This study examines how different HCV genotypes impact the effectiveness of interferon (IFN) treatment in chronic hepatitis C patients.
  • It was found that patients with genotype 1 had lower sustained viral response (SVR) rates (25.3%) compared to those with non-1 genotypes (43.2%), suggesting genotype 1 may lead to less effective treatment outcomes.
  • While Pegasys treatment led to comparable end-of-treatment viral response (ETVR) rates for both genotypes, the significant difference in SVR rates highlights the need for personalized treatment approaches based on HCV genotype.
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Objective: To study the role of tumor necrosis factor-alpha (TNFalpha) and caspase-3 expression on hepatocyte apoptosis in experimental model of fulminant hepatic failure (FHF).

Methods: Mouse experimental model of FHF was induced by lipopolysaccharide (LPS) and D-galactosamine (D-GalN). Serum TNFalpha level and TNFalpha mRNA expression in liver were tested by ELISA and reverse transcriptase PCR (RT-PCR) method, respectively.

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