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Cytokines profile in patients with acute and chronic hepatitis B infection
Camilla Rodrigues de Almeida Ribeiro1, Daniela Gois Beghini2, Andreza Salvio Lemos1
1Laboratory of Molecular Virology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Insights
Hepatitis B virus (HBV) infection elevates key cytokine levels, including tumor necrosis factor-alpha (TNF-α), interleukin-10 (IL-10), and IL-6, particularly in acute cases. These cytokines may play a role in viral clearance and preventing chronic infection.
Area of Science:
- Immunology
- Hepatology
- Virology
Background:
- Hepatitis B virus (HBV) is a major global health concern causing acute and chronic hepatitis.
- Immune responses, regulated by cytokines, are crucial in determining HBV infection outcomes (elimination or persistence).
- Understanding cytokine profiles in HBV infection is vital for developing effective therapeutic strategies.
Purpose of the Study:
- To determine the cytokine profiles (IFN-γ, TNF-α, IL-2, IL-4, IL-6, IL-10, and IL-17A) in patients with acute and chronic HBV infection.
- To investigate the association between these cytokine profiles and HBV genotypes.
- To explore the correlation between cytokine levels and disease severity (acute vs. chronic).
Main Methods:
- Analysis of 66 plasma samples from patients with acute (n=19) and chronic (n=47) HBV infection, plus 10 healthy controls.
- Biochemical tests, nested-PCR, and real-time PCR were performed.
- Cytokine levels were quantified using a BD Cytometric Bead Array Human Th1/Th2/Th17 Cytokine Kit.
Main Results:
- All measured cytokines were significantly elevated in HBV-infected individuals compared to healthy controls.
- Strong positive correlations were observed among IFN-γ, TNF, IL-10, IL-6, IL-4, and IL-2.
- Tumor necrosis factor-alpha (TNF-α), IL-10, and IL-6 levels were significantly higher in the acute hepatitis B group compared to chronic and control groups.
Conclusions:
- Cytokine profiles differ between acute and chronic HBV infection, with higher levels of TNF-α, IL-10, and IL-6 in acute cases.
- These specific cytokines may be involved in the host's immune response to eliminate HBV and prevent disease chronicity.
- No correlation was found between HBV genotypes, viral load, and the analyzed cytokine profiles.
Abstract:
Hepatitis B virus (HBV) is one of the leading causes of acute and chronic hepatitis and represents a serious public health threat. Cytokines are important chemical mediators that regulate the differentiation, proliferation, and function of immune cells, with accumulating evidence indicating that the inadequate immune responses are responsible for the elimination or persistence of HBV. This study aimed to determine the cytokine profiles (IFN-γ, TNF-α, IL-2, IL-4, IL-6, IL-10, and IL-17A) during HBV infection and investigate their association with genotypes. A total of 66 plasma samples, 19 from patients with acute and 47 with chronic hepatitis B infection, were subjected to biochemical tests, nested-PCR, and real-time PCR, with cytokines evaluated using a commercial BD Cytometric Bead Array Human Th1/Th2/Th17 Cytokine Kit. Healthy controls (10 individuals) were selected from blood donors with no history of liver diseases. No correlation was found between genotypes, viral load, and cytokines analyzed. All cytokines showed higher levels of production among infected individuals when compared with the control group. A positive correlation classified as moderate to strong was found between cytokines IFN-γ, TNF, IL-10, IL-6, IL-4, and IL-2 through the Spearman correlation coefficient. TNF (P = 0.009), IL-10 (P < 0.001), and IL-6 (P < 0.001) levels were higher in acute individuals compared with chronic and control groups. Theses cytokines could be involved in the elimination of virus and protection against chronicity.
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