Method for controlling incubator to be applicable to induction and amplification of immune cells
An immune cell and cell technology, applied in the direction of blood/immune system cells, animal cells, tissue culture, etc., can solve the problems of limited application of cellular immunotherapy, poor uniformity of immune cells, and high probability of tumorigenesis, and achieve the efficiency of induction differentiation The effect of improvement, uniformity improvement, and amplification efficiency improvement
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Embodiment 1
[0030] The following will introduce in detail the method of using the incubator according to the embodiment of the present invention, so that the incubator operates in the control method according to the embodiment of the present invention, and the method for inducing the expansion of immune cells, the method includes inducing isolated mononuclear cells Expand into immune cells, and detect the activity of immune cells.
[0031] 1. Experimental method
[0032] 1. Preparation of Anti-human CD16 Coated ZellWerk Bioreactors
[0033] 1.1 Add 15 mL of 2.5 μg / mL anti-human CD16 monoclonal antibody dissolved in medical normal saline to the bioreactor, shake the culture bottle gently to make the antibody cover the culture surface, and overnight at 4°C in the dark.
[0034] 1.2 Recover the antibody coating solution before use, wash the bioreactor once with 15mL of normal saline, and then use 15mL of T cell expansion medium (OpTmizer TM CTS TM T-cell expansion SFM) and washed once.
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Embodiment 2
[0079] 1. Experimental method
[0080] 1. Preparation of Anti-human CD16 Coated ZellWerk Bioreactors
[0081] 1.1 Add 15 mL of 2.5 μg / mL anti-human CD16 monoclonal antibody dissolved in medical normal saline to the bioreactor, shake the culture bottle gently to make the antibody cover the culture surface, and overnight at 4°C in the dark.
[0082] 1.2 Recover the antibody coating solution before use, wash the bioreactor once with 15mL of normal saline, and then use 15mL of T cell expansion medium (OpTmizer TM CTS TM T-cell expansion SFM) and washed once.
[0083] 2. Collect peripheral blood, separate peripheral blood plasma and mononuclear cells
[0084] 2.1 Collect about 100ml of human peripheral blood with a sterile blood collection bag added with anticoagulant, and reserve 1ml of peripheral blood for quick test and blood type identification. After passing the quick test, the peripheral blood will be sent to the GMP laboratory. If the quick test fails, the blood sample w...
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