PBMC induced TCM and application
An immune cell and memory technology, applied in the application field of memory immune cells (TCM), can solve the problems of difficult long-term survival of immune cells and lack of targeting, and can solve the problems of poor T cell proliferation and immune incompetence. Effect
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Embodiment 1
[0036] 1. Isolation and cryopreservation of PBMC cells:
[0037] a. Separation of PBMC cells: Peripheral blood was evenly divided into 50 mL centrifuge tubes with an electric aspirator, with no more than 35 mL per tube, 931 g, centrifuged for 8 min, and the upper layer of plasma was sucked into the 50 mL centrifuge tube, and 1.5 mL in EP tubes, labeled, and stored at -80°C. Dilute the blood cells with NA so that the ratio of blood cells: NA is 1:1, mix evenly and slowly add to the corresponding upper layer of liquid A to form a complete interface. 596 g, centrifuged for 20 min. Visible stratification. Aspirate and discard the supernatant of the first layer, and carefully and gently aspirate the second layer of white cell layer into different clean 50 mL centrifuge tubes. Add NA to each tube respectively, dilute and mix, and dilute to 40mL / tube. 931 g, centrifuged for 8 min. Discard the supernatant and add NA to resuspend the cells. The cell suspension was collected for c...
Embodiment 2
[0051] On the basis of Example 1, the TCM cells were sorted and purified, and induced and transfected in vitro, as follows
[0052] 1. Magnetic bead sorting of T cell subsets:
[0053] (1) Cell count.
[0054] (2) Prepare a single cell suspension (filtered with a 30-pore nylon mesh).
[0055] (3) Add buffer to wash cells, centrifuge at 1500rpm, 5min (4-8°C)
[0056] (4) Add 80ul / 107 cells of buffer.
[0057] (5) Add 20ul / 107 cells of antibody-coated magnetic beads.
[0058] (6) Incubate at 4-8°C for 10 minutes.
[0059] (7) Add 1ml / 107 cells of buffer to wash the cells and centrifuge at 1500rpm for 5min (4-8°C).
[0060] (8) Add 500ul / 107 cells of buffer to resuspend the cells.
[0061] (9) Prepare the separation column and wash the MS column with 500ul of buffer.
[0062] (10) Carefully add the cell suspension to the bottom surface of the sorting column.
[0063] (11) Rinse the column with 500ul of buffer solution (add new liquid each time there is no residual liquid)...
Embodiment 3
[0073] On the basis of embodiment 2 formula a, carry out the selection of induction formula
[0074] On the 1st day after isolation, the primary treatment was completed with 1000IU / ml IFN-γ, anti-human 130ng / ml CD3 monoclonal antibody, anti-human 110ng / ml CD28 monoclonal antibody, recombinant human 1000IU / ml IL-2, and 120u / mL IL-1α. Stimulate. Half of the medium was changed every 2 days, and recombinant human IL-2 (final concentration of 1000 IU / ml), 800 u / mL IL-7 and 800 u / mL recombinant human IL-15 were added.
[0075] The isolated PBMCs were resuspended with X-VIVO15, and the initial stimulation was completed with anti-human 130ng / mL CD3 monoclonal antibody, 110ng / mL anti-human CD28 monoclonal antibody and 1000u / mL recombinant human IL-2. The medium was changed in half every 2 days, and 1000 u / mL recombinant human IL-2 and 800 u / mL recombinant human IL-15 were added. On the basis of traditional TCM cell culture, IFN-γ, IL-1α and recombinant human cytokine IL-7 were added....
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