Human immunocompetent cell DC-CIK cytomedicine and effective preparation method thereof
A technology of DC-CIK and immune activity, applied in the field of human immunocompetent cell DC-CIK cell preparations and its effective preparation, can solve the problems of long culture time, hindering the promotion and application of DC-CIK cells, and low killing activity of DC-CIK cells problems, to achieve the effect of clearing residual lesions, enhancing specific anti-tumor immune response, and improving anti-cancer activity
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Embodiment 1
[0032] Example 1 Preparation of DC-CIK cells
[0033] 1.1 Preparation of DC-CIK cells optimized by the present invention (experimental group)
[0034] The specific preparation steps are as follows: the peripheral blood of the patient is collected, and mononuclear cells are separated by density gradient centrifugation of human lymphocyte separation fluid. Inoculate mononuclear cells into serum-free medium and adjust the cell concentration to 2x10 6 / m1, add IFN-γ (2000U / m1), IL-4 (500U / m1), GM-CSF (800U / m1) at 37℃ 5%C0 2 Culture under conditions, add IL-2 (1000U / m1), IL-15 (20ng / m1), anti-CD3 monoclonal antibody (50ng / m1) to continue culture after 1 day, add TNFα (500U / m1) to promote DC after 3 days Cells mature. After 4 days, IL-2 (1000 U / m1) and IL-15 (20 ng / m1) were added and cultured for 8 days to obtain DC-CIK cells.
[0035] 1.2 Preparation of routine protocol for DC-CIK cells before optimization (control group)
[0036] The specific preparation steps are as follows:...
Embodiment 2
[0037]Example 2 Determination of cell number, cell phenotype and killing activity to cancer cells
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