Method of amplifying natural killer T cells
A natural killer and cell technology, applied in animal cells, vertebrate cells, cell culture active agents, etc., can solve problems such as difficult access to cellular immunotherapy
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Embodiment 1
[0052]Example 1. Human Vα24 + Expansion of NKT cells
[0053] (1) Preparation of PBMCs and preparation of G-PBSCs
[0054] Buffy coats (crude PBMCs) prepared from 400 ml of whole blood from healthy individuals were provided by the Japanese Red Cross Blood Center. Cellular fractions containing PBSCs (crude G-PBSCs) were obtained from chemotherapy-treated patients who received G-CSF subcutaneously at a dose of 100-250 μg / person / day for 6-10 days after chemotherapy (Table 1 ), within 2-24 hours of the last G-CSF injection, with COBE Spectra TM Cell Separator (LAKE WOOD, CO USA 80215) to complete apheresis (Hematopoietic Stem Cells: Applications in Biology and Therapeutics. Levit DJ, Mertelsmann R (eds), Marcel Dekker, Inc., New York, 1995, 611- 630).
[0055] From the obtained crude PBMCs and crude G-PBSCs, mononuclear cell fractions (referred to as "PBMCs" and "G-PBSCs", respectively) were prepared using Lymphosepal density gradient medium (Immuno-Biological Laboratories Gun...
Embodiment 2
[0068] Example 2 Evaluation of Vα24 + Cytotoxic activity of NKT cells against human tumor cells
[0069] Purification of human Vα24 from day 12 cultured cells using the FACS Vantage cell sorting system + NKT cells, and the cytotoxic activity of these cells against tumor cells and the cytokine production activity of these cells were assessed.
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