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Establishment of Epstein-Barr Virus Growth-transformed Lymphoblastoid Cell Lines
Published on: November 8, 2011
Composite Epstein-Barr Virus-associated T-lymphoblastic and Peripheral T-cell Lymphomas: A Clonal Study
Hiroki Hosoi1, Toshiki Mushino1, Kazutaka Nakashima2
1Department of Hematology/Oncology, Wakayama Medical University, Japan.
Epstein-Barr virus (EBV) may infect immature T-cells expressing CD21, leading to T-lymphoblastic lymphoma (T-LBL). This can evolve into CD21-negative peripheral T-cell lymphoma (PTCL-NOS) at relapse, suggesting a phenotypic shift.
Area of Science:
- Virology
- Oncology
- Immunology
Background:
- Epstein-Barr virus (EBV) is associated with various lymphoid malignancies.
- T-lymphoblastic lymphoma (T-LBL) is an aggressive lymphoma originating from immature T-cells.
- Peripheral T-cell lymphoma, not otherwise specified (PTCL-NOS) represents a heterogeneous group of mature T-cell neoplasms.
Observation:
- A patient initially diagnosed with T-lymphoblastic lymphoma (T-LBL) harbored a clonal Epstein-Barr virus (EBV) genome.
- At relapse, the patient presented with axillary lymphadenopathy diagnosed as peripheral T-cell lymphoma, not otherwise specified (PTCL-NOS).
- Southern blot analyses confirmed that both the T-LBL and PTCL-NOS were clonally identical, indicating a common origin.
Findings:
- The initial T-LBL cells expressed CD21, which facilitated EBV entry.
- The relapsed PTCL-NOS cells lacked CD21 expression.
- The clonal identity between T-LBL and PTCL-NOS suggests a transformation or evolution of the lymphoma.
Implications:
- This case suggests a potential pathway where EBV infects immature CD21-positive T-cells, initiating lymphomagenesis.
- The emergence of CD21-negative PTCL-NOS from CD21-positive T-LBL implies a possible phenotypic switch during disease progression.
- Understanding this evolution could offer insights into T-cell lymphoma pathogenesis and EBV-driven malignancies.
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