In-vitro large-scale amplification method of natural killer cells
A natural killer cell, large-scale technology, applied in the field of human cell culture, can solve the problems of difficult expansion, unable to meet the number of clinical reinfusion cells, cumbersome operation, etc.
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Embodiment 1
[0060] The in vitro large-scale expansion method of natural killer cells in this embodiment is carried out according to the following steps:
[0061] 1 Collect peripheral blood mononuclear cells (PBMC) from the donor.
[0062] Directly draw 80-100mL of venous blood from the donor, and add anticoagulant—heparin;
[0063] 2. Isolation of PBMCs
[0064] 2.1 Centrifuge at 2000rpm for ten minutes at room temperature, carefully absorb the upper plasma layer, inactivate in a 56-degree water bath for 30 minutes, centrifuge at 4000rpm for 10 minutes, carefully absorb the supernatant and store it at 4°C for later use.
[0065] 2.2 Dilute the patient's blood sample with sterile saline at a ratio of 1:1 to reduce the loss of PBMC. After mixing well, slowly add the blood sample into the 50mL centrifuge tube filled with lymphocyte separation medium at a ratio of 1:1.
[0066] 2.3 Horizontal centrifugation: speed 2000rpm, 30min.
[0067] 2.4 After the centrifugation is completed, the abs...
Embodiment 2
[0095] The large-scale in vitro expansion method of natural killer cells in this example differs from Example 1 in that: the anticoagulant added to the venous blood collected in step 1 is sodium citrate; the centrifuge used in step 2.4 Tubes are 250 mL capacity; step 4.4 is performed on day 4; step 4.5 is performed on day 6; step 4.6 is performed on day 9; step 4.8 is performed on day 12; step 4.9 is performed on day 15.
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