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Updated: Jul 10, 2026

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An Efficient and Simple Method to Establish NK and T Cell Lines from Patients with Chronic Active Epstein-Barr Virus Infection
Published on: March 30, 2018
In vitro methods for generating highly purified EBV associated tumor antigen-specific T cells by using solid phase T
Jongming Li1, Bijoyesh Mookerjee, John Wagner
1Department of Medical Oncology, 1024 Curtis Building, Thomas Jefferson University, Philadelphia, PA 19107, USA. jongming.li@jefferson.edu
Journal of Immunological Methods
|October 13, 2007
Summary
This study introduces a novel method for purifying tumor antigen-specific T cells, enhancing adoptive cell transfer immunotherapy for EBV-related cancers. The new system rapidly increases T cell purity and quantity, offering a simpler, faster, and cheaper alternative.
Area of Science:
- Immunology
- Cell Biology
- Cancer Therapy
Background:
- Adoptive cell transfer (ACT) immunotherapy is used for Epstein-Barr virus (EBV)-related malignancies.
- Current methods for purifying tumor antigen-specific T cells are limited.
- Effective T cell purification is crucial for successful ACT immunotherapy.
Purpose of the Study:
- To develop a novel solid-phase T cell selection system for antigen-specific T cell purification.
- To improve the efficiency and speed of generating tumor antigen-specific T cells for ACT.
- To overcome limitations of traditional T cell expansion methods.
Main Methods:
- A novel solid-phase T cell selection system using immobilized monocytes or EBV-transformed B-lymphocytes.
- Utilizing the differential binding kinetics of antigen-specific T cells to cognate antigens.
- Optimizing selection time for EBV-specific and LMP2-specific T cells.
Main Results:
- The system achieved >20-fold enrichment of antigen-specific T cells.
- Activated antigen-specific T cells demonstrated enhanced proliferation.
- The method significantly increased T cell frequency and purity.
Conclusions:
- The novel T cell selection system is simple, rapid, and inexpensive.
- It is superior to traditional methods for generating tumor antigen-specific T cells.
- This system facilitates the generation of highly purified T cells for ACT immunotherapy within two weeks.

