Composition for efficiently inducing and amplifying human peripheral blood killer immune cells, kit and culture method of immune cells
A technology of immune cells and culture methods, which is applied in the field of compositions for efficiently inducing and expanding killer immune cells in human peripheral blood, which can solve the problems of reduced curative effect of drugs, unsatisfactory effects, and influence on the normal function of the immune system, and achieve the goal of easy use Effect
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Embodiment 1
[0054] The culturing steps of PDCT cells (T cells+DC cells) provided by the present invention are as follows:
[0055] 1. Collection of peripheral blood mononuclear cells
[0056] Use a blood cell separator to collect the patient's own peripheral blood mononuclear cells 1-2*10 8 (or draw 80ml of autologous peripheral blood).
[0057] 2. Inactivated plasma
[0058] 2.1. Add the obtained peripheral blood into a 50ml centrifuge tube and centrifuge at 1000g for 5min;
[0059] 2.2. Use a pipette to carefully extract 10ml of the upper layer of plasma (do not draw to the boundary layer), add 10ml of normal saline to the centrifuge tube, and obtain peripheral blood and 10ml of plasma after plasma extraction;
[0060] 2.3. Inactivate 10ml of the obtained plasma in a water bath at 56°C for 30 minutes;
[0061] 2.4. Take out the inactivated plasma, put it into a centrifuge tube, centrifuge at 2000g for 5min, take the supernatant, and put it in a 4°C refrigerator for later use.
[00...
Embodiment 2
[0121] The culturing steps of PDCT cells (T cells+DC cells) provided by the present invention are as follows:
[0122] 1. Collection of peripheral blood mononuclear cells
[0123] Use a blood cell separator to collect the patient's own peripheral blood mononuclear cells 1-2*10 8 (or draw 80ml of autologous peripheral blood).
[0124] 2. Inactivated plasma
[0125] 2.1. Add the obtained peripheral blood into a 50ml centrifuge tube and centrifuge at 1000g for 5min;
[0126] 2.2. Use a pipette to carefully extract 10ml of the upper layer of plasma (do not draw to the boundary layer), add 10ml of normal saline to the centrifuge tube, and obtain peripheral blood and 10ml of plasma after plasma extraction;
[0127] 2.3. Inactivate 10ml of the obtained plasma in a water bath at 56°C for 30 minutes;
[0128] 2.4. Take out the inactivated plasma, put it into a centrifuge tube, centrifuge at 2000g for 5min, take the supernatant, and put it in a 4°C refrigerator for later use.
[01...
Embodiment 3
[0188] The culturing steps of PDCT cells (T cells+DC cells) provided by the present invention are as follows:
[0189] 1. Collection of peripheral blood mononuclear cells
[0190] Use a blood cell separator to collect the patient's own peripheral blood mononuclear cells 1-2*10 8 (or draw 80ml of autologous peripheral blood).
[0191] 2. Inactivated plasma
[0192] 2.1. Add the obtained peripheral blood into a 50ml centrifuge tube and centrifuge at 1000g for 5min;
[0193] 2.2. Use a pipette to carefully extract 10ml of the upper layer of plasma (do not draw to the boundary layer), add 10ml of normal saline to the centrifuge tube, and obtain peripheral blood and 10ml of plasma after plasma extraction;
[0194] 2.3. Inactivate 10ml of the obtained plasma in a water bath at 56°C for 30 minutes;
[0195] 2.4. Take out the inactivated plasma, put it into a centrifuge tube, centrifuge at 2000g for 5min, take the supernatant, and put it in a 4°C refrigerator for later use.
[01...
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