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Updated: Aug 30, 2026

Stem Cell-Derived Viral Ag-Specific T Lymphocytes Suppress HBV Replication in Mice
Published on: September 25, 2019
[Dendritic cells originated from the peripheral blood in chronic hepatitis B patients can induce specific T cell
Ruo-bing Li1, Hong-song Chen, Yao Xie
1Institute of Hepatology, People's Hospital, Peking University, Beijing 100044, China.
Insights
Dendritic cells (DCs) from chronic hepatitis B patients can be stimulated with a specific hepatitis B virus (HBV) peptide to generate antigen-specific T cells. These T cells can effectively kill HBV-infected cells, offering a potential therapeutic strategy.
Area of Science:
- Immunology
- Hepatology
- Virology
Context:
- Chronic hepatitis B (CHB) is a significant global health concern.
- Understanding T cell immune responses in CHB is crucial for developing effective therapies.
- Dendritic cells (DCs) play a key role in initiating adaptive immune responses.
Purpose:
- To investigate the capacity of dendritic cells (DCs) from CHB patients to induce a specific T cell immune response against HBV.
- To assess the functional capacity of T cells generated by DCs pulsed with a specific HBV epitope peptide.
Summary:
- Peripheral blood mononuclear cells (PBMCs) from CHB, acute hepatitis B (AHB), and normal donor (ND) groups were analyzed for T cell responses to an HBcAg epitope peptide.
- DCs generated from CHB patients' PBMCs were pulsed with the HBcAg peptide and co-cultured with autologous lymphocytes.
- The study assessed the induction of antigen-specific T cells using intracellular cytokine staining and cytotoxic assays.
Impact:
- The findings demonstrate that DCs from CHB patients can be effectively used to generate HBV antigen-specific T cells.
- These induced T cells exhibit cytotoxic activity against target cells and produce cytokines essential for viral clearance.
- This research highlights a potential immunotherapeutic approach for managing chronic hepatitis B.
Objective:
To study whether dendritic cells (DCs) derived from the peripheral blood in chronic hepatitis B patients can induce specific T cell immune response.
Methods:
(1)The subjects were divided into 3 groups: chronic hepatitis B group (CHB), acute hepatitis B group (AHB), and normal donor group (ND). The peripheral blood mononuclear cells (PBMCs) isolated from those subjects were stimulated with HBcAg 18 to 27 CTL epitope peptide, and intracellular cytokine staining (ICCS) was used for detecting IFN-gamma, IL-2 and TNF-alpha produced by CD8+ T cell. (2) DCs generated from PBMCs were pulsed with HBcAg 18 to 27 CTL epitope peptide, then were cocultured with autologous lymphocytes for 10 days to induce antigen-specific T cell, which was assessed by ICCS and cytotoxic assay.
Results:
(1) The memory effect of the PBMCs from AHB group to HBcAg 18 to 27 CTL epitope peptide was stronger than that from CHB or ND group (t=2.508-3.305, P<0.05). (2)After lymphocytes were cocultured with DC treated with HBcAg 18 to 27 CTL epitope peptide, antigen-specific T cell effect was induced. And the killing rates were (57.0+/-23.0)%, (49.5+/-20.2)%, (21.8+/-12.9)% at the effector/target of 30:1, 10:1, 3:1, which were higher than that in control group.
Conclusions:
The memory T cells against HBV antigen lacks in CHB patients. DCs from CHB patients pulsed with HBcAg 18 to 27 epitope peptide can induce HBV antigen-specific T cell, which can kill specific target cells and produce cytokines involved in virus clearance.
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