Freezing resuscitation solution for multi-cytokine-induced killer cells, and applications thereof
A technology for killing cells and cytokines, which is applied in the field of bioengineering and can solve problems such as the clinical application of inappropriate cell products
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Embodiment 1
[0052] 1. PBMC recovery
[0053] (1) Peripheral blood mononuclear cells (PBMCs) cryopreserved in liquid nitrogen were taken out and rapidly thawed in a water bath at 37-42°C.
[0054] (2) The cells were treated with an equal volume of X-VIVO15 medium (referred to as group P) and an equal volume of recovery solution containing 2.5% HSA and 5% Dextran40 (referred to as group F1).
[0055] (3) Centrifuge, take the cells separately, count with a cell viability analyzer, and measure the cell viability.
[0056] 2. Induced into CIK cells
[0057] Cells in group P and group F1 were cultured statically for 24 hours in X-VIVO15 medium, respectively. Then, 1000U / ml IFN-γ and 2.5% Supgrow were added to the cell culture medium of the P group and the F1 group, after continuing to culture for 24 hours, 100ng / ml CD3, 1000U / ml IL-2, 1000U / ml IL-1α were added, Perform in vitro induction amplification.
[0058] 3. Calculate
[0059] Since the number of initial cells is inconsistent when re...
Embodiment 2
[0086] 1. Cord blood MNC resuscitation
[0087] (1) The cryopreserved umbilical cord blood mononuclear cells (MNC) were taken out from liquid nitrogen and rapidly thawed in a water bath at 37-42°C.
[0088] (2) Use equal volumes of X-VIVO15 medium (referred to as P group), and equal volumes of resuscitation fluid containing 2.5% HSA and 5% Dextran40 (referred to as F1 group), 2.5% plasma, 5% Dextran40 Cells were treated in four ways with resuscitation solution (referred to as F2 group), resuscitation solution with 5% plasma and 5% Dextran40 (referred to as F3 group).
[0089] (3) Centrifuge, take the cells separately, and use a cell viability analyzer to count and measure the cell viability.
[0090] 2. Induced into CIK cells
[0091] The cells treated in groups P and F1-3 were cultured statically for 24 hours in X-VIVO15 medium, respectively. The cells treated in the P and F1-3 groups were treated by adding 1000U / ml IFN-γ and 2.5% Supgrow, and continued to culture for 24 h...
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