All procedures involving sample collection have been performed in accordance with the institute's IRB guidelines.
1. Isolation of PBMCs and enrichment/purification of NK cells
NOTE: Other methods for the isolation of peripheral blood mononuclear cells (PBMCs) and enrichment/purification can also be performed.
- Draw 200 mL of blood under regulated conditions into a tube containing heparin.
- Add 15 mL of the density gradient medium into a 50 mL tube with a porous barrier incorporated. Spin the tube at 1000 x g for 30 s.
- Add 12.5 mL of blood into the tube, followed by another 12.5 mL of PBS, and gently invert 3x. Spin the tube at 800 x g for 15 min at room temperature (RT) with no breaks.
- Prepare a 50 mL conical tube with 40 mL of PBS for each tube with a porous barrier while the cells are spinning.
- Carefully remove the tubes and inspect after centrifugation. Check for a thin, visibly white layer of PBMCs above the porous barrier, between the 20 mL and 25 mL demarcations on the 50 mL tube.
- Carefully remove as much liquid as possible from the top using a pipette without disturbing the thin, white PBMC layer.
- With a clean 10 mL serological pipette, gently remove the PBMC layer in addition to the clear, yellowish liquid layer down to the filter of the tube.
- Expel the PBMCs and liquid into the 50 mL conical containing PBS prepared in step 1.4. Spin tubes at RT and 300 x g for 5 min.
- Aspirate the PBS wash and add an additional 40 mL of PBS. Spin tubes at RT and 300 x g for 5 min.
- After washing, count the cells and resuspend them in 40 µL of 2% BSA/PBS per 1 x 107 cells.
- Proceed to the isolation of NK cells using the method of choice. Choices include manual or automated magnetic bead-based sorting. Fluorescence-activated cell sorting can also be performed.
- Remove a small aliquot of cells to determine the purity of NK cells by flow cytometry. Gating strategy includes the following: gate on live cells based on forward vs. side scatter profile, then assess the purity based on NK markers (e.g., CD3, CD56) in the specific live population. Typical purity is >95%.
- After isolation is completed, spin cells at RT and 300 x g for 5 min to pellet and aspirate.
- Resuspend the cell pellet to 1 x 107 cells/mL in RPMI 1640 with nutrients, 10% heat-inactivated FBS, 1 mM sodium pyruvate, 55 mM 2-ME, and 10 mM HEPES (pH = 7.2).
2. Antibody-mediated activation of NK cells via FcγRIIIa
- Set a refrigerated microcentrifuge to 4 °C.
- Dispense 1 x 106 (100 µL of) resuspended NK cells into 1.5 mL tube(s) and place on ice.
NOTE: Cells can be dispensed into a 96 well U-bottom plate if there are numerous samples.
- Prepare 1 µL of 100 µg/mL rituximab (or antibody of interest) per sample and add 1 µL to the cells for a final concentration of 1 μg/mL antibody.
NOTE: Other molecules can be added to the cells at this point or earlier for the assessment of combination effects. Here, ritixumab was used for stimulation. In prior studies, small molecule inhibitors have been added to stimulations.
- Incubate the sample on ice for 30 min. During incubation, prepare 50 μL of 50 µg/mL anti-human κ light chain antibody per sample in media and warm to 37 °C on a heat block or in a water bath.
- After incubation of cells on ice, add 1 mL of ice-cold media and spin at 135 x g for 5 min at 4 °C. Wash again with 1 mL of ice-cold media.
- Aspirate the supernatant after the last wash and add 50 µL of the anti-human κ light chain mixture prepared in step 2.4.
- Immediately incubate samples for the end-user-determined timepoints at 37 °C on a heat block or in a water bath.
- Stop stimulation by adding 1 mL of ice-cold media and immediately spin samples in a refrigerated centrifuge at 135 x g for 5 min. Wash once more with 1 mL of ice-cold media.
