Efficient transduction with recombinant adenovirus in EBV-transformed B lymphoblastoid cell lines

  • Hye Jin Kim
  • , Hyun Il Cho
  • , Yoon Hee Han
  • , Soo Young Park
  • , Dong Wook Kim
  • , Dong Gun Lee
  • , Jee Hoon Kim
  • , Wan Shik Shin
  • , Soon Young Paik
  • , Chun Choo Kim
  • , Young Seon Hong
  • , Tai Gyu Kim

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

The Epstein-Barr-transformed B lymphoblastoid cell lines, LCL, which express antigens, are potential antigen-presenting cells (APCs) for the induction of cytotoxic T lymphocytes in vitro. However, transfecting LCL with subsequent selection by antibiotics is notoriously difficult because the plating efficiencies of LCL are reported to be 1% or less. Therefore, this study investigated the optimal conditions for increasing the transduction efficiency of a recombinant adenovirus to LCL for use as a source of APCs. The transduction efficiencies were < 13% (SD ± 2.13) at a multiplicity of infection (MOI) of 100, while it was increased to 28% (SD ± 9.43) at an MOI of 1000. Moreover, its efficiencies to LCL that expressed the coxsackie adenovirus receptor were increased to 60% (SD ± 6.35) at an MOI of 1000, and were further increased to 70% (SD ± 4.56) when combined with the centrifugal method. The cationic liposome or anionic polymer had no effect on the transduction efficiency when compared to that of the centrifugal method. These results may be used as a convenient source of target cells for a CTL assay and/ or autologous APCs for the induction of the in vitro CTL responses that are specific to viral and tumor antigens.

Original languageEnglish
Pages (from-to)376-382
Number of pages7
JournalJournal of Biochemistry and Molecular Biology
Volume37
Issue number3
DOIs
StatePublished - 31 May 2004

Keywords

  • Adenovirus
  • Centrifuge
  • Coxsackievirus and adenovirus receptor
  • EBV-transformed B lymphoblastoid cell lines
  • Gene transfer

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