[Detection, enrichment and expansion of T lymphocytes mediating alloresponse based on cytokine]

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2006 Jan;35(1):39-44. doi: 10.3785/j.issn.1008-9292.2006.01.008.
[Article in Chinese]

Abstract

Objective: To detect, enrich and expand the cytokine secreting T lymphocytes after allogeneic PBMNCs stimulation.

Methods: The novel cytokine secretion assay (CKSA) was applied to detect T lymphocytes secreting IFN-gamma at single cell level in human mixed lymphocytes reaction. IFN-gamma secreting T cells were enriched by means of magnetic sorting system and expanded with OKT(3), anti-CD(3)mAb and IL-2 combination. Antigen specificity of the expanded cells was confirmed using enzyme linked immunospot assay.

Results: A sizable proportion of IFN-gamma secreting T lymphocytes could be detected [(1.12 +/-0.13)% compared with (0.23 +/-0.07)%] and be further enriched to (67.3 +/-10.5)%, or (93.8 +/-22.1) fold. T lymphocytes could be expanded up to 600-fold within 21-28 days and the specific IFN-gamma response of expanded cells was confirmed with stimulation of the relevant allogeneic PBMNC, which was significantly higher than the irrelevant PBMNC control.

Conclusion: It is feasible to detect significantly increased IFN-gamma secreting T lymphocytes after allogeneic PBMNCs stimulation based on the CKSA technique at single cell level and these cells can be efficiently enriched and expanded for further research.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / pharmacology
  • CD28 Antigens / immunology
  • Cell Proliferation
  • Cells, Cultured
  • Cytokines / metabolism*
  • Graft vs Host Disease / immunology*
  • Humans
  • Interferon-gamma / metabolism*
  • Interleukin-2 / metabolism
  • Leukocytes, Mononuclear / cytology*
  • Leukocytes, Mononuclear / immunology
  • Lymphocyte Culture Test, Mixed
  • Muromonab-CD3 / pharmacology
  • T-Lymphocytes / cytology*
  • T-Lymphocytes / immunology

Substances

  • Antibodies, Monoclonal
  • CD28 Antigens
  • Cytokines
  • Interleukin-2
  • Muromonab-CD3
  • Interferon-gamma