An in vitro activation method of cytokine-induced killer cells
A technology for killing cells and cytokines, applied in the field of biomedicine, can solve the problems of lack of functional cells, not increasing the proportion of NK cells, etc., and achieve the effect of reducing the cost of in vitro expansion and culture, large market prospects and economic value
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Embodiment 1
[0040] This embodiment discloses a method for in vitro activation and culture expansion of cytokine-induced killer cells (CIK cells). Taking 40ml of human peripheral blood as an example, the method is as follows:
[0041] 1. Cell Culture and Harvesting
[0042] (1) Preparation of 2% gelatin: Weigh 2 g of gelatin (product of Sigma, USA, product number G7041), weigh 0.85 g of sodium chloride, and add 90 ml of deionized water. Stir to dissolve, add deionized water to adjust the total volume to 100ml. Filter through a 0.22 μm syringe filter. Store at 4°C.
[0043] (2) Coating of activator: prepare two bottom areas of 75cm 2 The culture flasks are marked as ctr and test respectively. Add physiological saline to the culture bottle marked as ctr, add 10ml of 2% gelatin (activator) to the culture bottle marked as test, and spread it on the bottom of the culture bottle. Place the flask at 37°C for 2 hours.
[0044] It should be noted that ctr represents a traditional method, and ...
Embodiment 2
[0081] This embodiment discloses a method for in vitro culture and expansion of cytokine-induced killer cells (CIK cells). Taking 50ml of human peripheral blood as an example, the method is as follows:
[0082] 1. Cell Culture and Harvesting
[0083] (1) Coating with activator: prepare 4 pieces with a bottom area of 75cm 2 The culture flasks are marked as ctr and test respectively. Add physiological saline to the culture bottle marked as ctr, add 10ml of 2% gelatin (activator) to the culture bottle marked as test, and spread it on the bottom of the culture bottle. Place the flask at 4°C overnight.
[0084] (2) Activator treatment: suck off the gelatin in the culture bottle marked as test, add physiological saline, shake gently to spread the salt level on the bottom of the culture bottle, and suck out the normal saline. Aspirate the normal saline in the culture flask marked as ctr. The culture bottle is ready for use.
[0085] (3) Take 50ml of peripheral blood from healt...
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