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VDJ-Seq: Deep Sequencing Analysis of Rearranged Immunoglobulin Heavy Chain Gene to Reveal Clonal Evolution Patterns of B Cell Lymphoma
Published on: December 28, 2015
HBV-associated DLBCL of poor prognosis: advance in pathogenesis, immunity and therapy
Xin Wan1, Ken H Young2, Ou Bai1
1Department of Hematology, The First Hospital of Jilin University, Changchun, Jilin, China.
Insights
Hepatitis B virus (HBV) infection is linked to worse outcomes in diffuse large B-cell lymphoma (DLBCL). This review explores HBV-associated DLBCL biology and potential new treatments.
Area of Science:
- Oncology
- Virology
- Immunology
Background:
- Hepatitis B virus (HBV) infection is associated with B-cell lymphoma, particularly diffuse large B-cell lymphoma (DLBCL).
- HBV-associated DLBCL presents with advanced stage, poor treatment response, and worse prognosis.
- Pathological hallmarks include abnormal nuclear factor kappa B pathway activation and oncogene mutations (e.g., Myc, BCL-6).
Purpose of the Study:
- To comprehensively review the natural history of HBV infection and immunity in the context of DLBCL.
- To elucidate the mechanisms underlying HBV-associated DLBCL, including oncogenes, immune evasion, and signaling pathways.
- To identify potential therapeutic strategies for improving outcomes in HBV-associated DLBCL.
Main Methods:
- Mechanistic analysis of HBV infection and immunity.
- Review of HBV-mediated oncogenes and their role in lymphomagenesis.
- Analysis of immune escape mechanisms and epigenetic alterations in HBV-associated DLBCL.
- Examination of dysregulated signaling pathways implicated in the disease.
- Identification and discussion of potential therapeutic targets and approaches.
Main Results:
- HBV infection contributes to DLBCL pathogenesis through various mechanisms.
- Specific molecular alterations and immune dysregulation are characteristic of HBV-associated DLBCL.
- Current treatment strategies show limited efficacy, highlighting the need for novel approaches.
Conclusions:
- A deeper understanding of HBV-associated DLBCL biology is crucial for developing targeted therapies.
- Further research and clinical trials are needed to improve treatment efficacy and patient prognosis.
- Novel therapeutic strategies may emerge from a comprehensive understanding of HBV's role in DLBCL.
Abstract:
Advanced studies have shown a biological correlation between hepatitis B virus (HBV) and B-cell lymphoma, especially diffuse large B-cell lymphoma (DLBCL). Patients with DLBCL infected with HBV (HBV-associated DLBCL) are clinically characterized by an advanced clinical stage, poor response to front-line immunochemotherapy regimens, and worse clinical prognosis. HBV-associated DLBCL often exhibits abnormal activation of the nuclear factor kappa B pathway as well as mutations in oncogenes, including Myc and BCL-6. Currently, there is no consensus on any specific and effective treatment for HBV-associated DLBCL. Therefore, in this review, we comprehensively and mechanistically analyzed the natural history of HBV infection and immunity, including HBV-mediated oncogenes, immune escape, epigenetic alterations, dysregulated signaling pathways, and potential therapeutic approaches for HBV-associated DLBCL. We hope that an improved understanding of the biology of HBV-associated DLBCL would lead to the development of novel therapeutic approaches, enhance the number of effective clinical trials, and improve the prognosis of this disease.
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