Natural killer cell and cultivation method thereof
A technology of natural killer cells and cells, applied in the field of natural killer cells and their culture, can solve the problems such as the inability of NK cells to be widely used in clinical practice, the technical difficulty of separating and purifying NK cells, and the difficulty in avoiding T lymphocyte contamination, and achieve fast cell growth. , Wide application value, low cost effect
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Embodiment 1
[0036] The establishment of embodiment 1, NKG cell line
[0037] 1. Cell isolation
[0038] 1. Peripheral blood sample: Take 10ml of peripheral blood from a patient with non-Hodgkin's lymphoma, anticoagulate with heparin, and obtain the consent of the patient.
[0039] 2. Separation of peripheral blood mononuclear cells: After diluting the anticoagulated peripheral blood specimen with 10ml sterile PBS solution, carry out density gradient centrifugation with lymphocyte separation medium, 2200 rpm, 30 minutes, 20 degrees; For mononuclear cells, wash 3 times with PBS solution, 1500 rpm, 10 minutes, 20 degrees; use 250 μl sterile PBS solution to resuspend cells, count, and the cell concentration is 1.1×10 7 / 250μl, store at 4 degrees, and set aside.
[0040] 3. Separation and purification of NK cells: Add 20 μl of non-specific mouse IgG to the above cell solution at 4 degrees for 30 minutes to block non-specific binding. Add 100 μl CD56 MicroBeads to the cell solution, shake an...
Embodiment 2
[0047] Embodiment 2, the preparation of the culture method of NKG cell and NKG cell injection
[0048] 1. Exploration of training conditions
[0049] Inactivation of newborn bovine serum and horse serum: Place newborn bovine serum and horse serum free of bacteria, mycoplasma and virus contamination in a constant temperature water bath at 56°C for 30 minutes to inactivate complement, then store in a refrigerator at 4°C for later use.
[0050] Prepare the following media:
[0051] 1) Preparation of complete α-MEM liquid medium
[0052] Get α-MEM liquid culture medium (containing L-glutamine, sodium bicarbonate, ribonucleoside and deoxyribonucleoside) 800ml, add the following substances respectively, and the final concentration of this substance in the culture medium is in brackets: newborn cow Serum (10%, v / v), horse serum (10%, v / v), human interleukin 2 (1.0×10 5 IU / L).
[0053] 2) Preparation of complete α-MEM dry powder medium
[0054] Take 1 bag of α-MEM powder (10.2g, ...
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