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Dendritic cells transfected with lentiviral vector-encoding human granulocyte-macrophage colony-stimulating factor augment anti-tumour T-cell response in vitro

  • J. Cui
  • , A. L. Lin
  • , Q. Liu
  • , Q. Sun
  • , Z. H. Gao
  • Shandong University
  • The Third People's Hospital of Hangzhou City
  • University of Calgary and Calgary Laboratory Services

科研成果: 期刊稿件 › 文章 › 同行评审

2 引用 (Scopus)

摘要

Dendritic cells (DC) are professional antigen-presenting cells that can actively taken up and present tumour-derived proteins to induce a tumour-specific immune response. Granulocyte-macrophage colony-stimulating factor (GM-CSF) plays a pivotal role in the generation, sensitization, maturation and survival of DC. We charged the peripheral blood monocyte cell-derived DC with tumour lysate, and then transfected the DC with lentiviral vector-encoding human GM-CSF (hGMCSF). The antigen-presenting capacity of the hGM-CSF-transfected DC was tested by means of the mixed lymphocyte reaction and cytotoxic T-lymphocyte assay using wild-type DC as the control. The Lenti-hGM-CSF-transfected DC was able to stimulate the proliferation of naive allogeneic T lymphocytes and to generate tumour-specific cytotoxic T lymphocytes more efficiently than the wild-type DC. This data indicates that Lenti-hGMCSF-transfected DC could potentially be used as an effective clinical approach for cancer immunotherapy.

源语言英语
页(从-至)329-336
页数8
期刊International Journal of Immunogenetics
卷37
期5
DOI
出版状态已出版 - 10月 2010
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