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4 protocols using nkg2a apc

1

Multiparametric Flow Cytometry Analysis of Natural Killer Cells

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MNCs were stained with labeled antibodies, CD3 ECD (Biolegend), CD45 Krome Orange (R&D systems), CD56 PE-Cy5 (Biolegend), CD16 APC-Cy7 (Biologend), CD326 PerCPCy5.5 (Biolegend). Phenotypic analysis was performed using DNAM-1 FITC (Becton Dickinson), 2B4 FITC (Biolegend), NKG2A APC (Beckman Coulter), NKG2D APC (Biolegend), NKp30 PE (Biolegend) and NKp46 PE(Biolegend), isotype controls for IgG1 and IgG2a, (all Biolegend). Dead cells were stained with 1:1000 diluted sytox blue (Life Technologies; Invitrogen). Flow cytometry analysis was performed on a Gallios flow cytometer from Beckman Coulter. Analysis was done in Kaluza 1.5 (Beckman Coulter). Gating strategy is shown in Supplementary Figure 1.
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2

Phenotyping of HSPC-derived NK Cells

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HSPC-NK cell phenotype was determined by staining for CD56-PE-Cy7 (Biolegend, #318318), NKG2A-APC (Beckman Coulter, #A60797), CD16-FITC (Biolegend, #302006), pan-KIRs-PE (Biolegend, #339506, 312606 and 312708), DNAM-1-FITC (BD, #559788), NKp46-PE (Biolegend, #331908) and NKG2D-APC (Biolegend, #320808) (CellGro vs NK MACS) or CD56-BV510 (Biolegend, #318340), CD45-BV421 (Biolegend, #368522), NKG2A-PE-Cy7 (Beckman Coulter, #B10246), DNAM-1-FITC (Biolegend, #337104), NKp46-PE (Biolegend, #311908), NKp44-PE (Biolegend, #325108), NKp30-APC (Biolegend, #325210) and NKG2D-APC (Biolegend, #320808) (GMP validations runs). Briefly, 200.000 cells were washed using PBS/0.5% BSA and incubated with antibodies in PBS/0.5% BSA at 4 °C for 30 min. Cells were then washed twice with PBS/0.5% BSA and resuspended in PBS/0.5% BSA containing Sytox Blue (1:5000 diluted, invitrogen, #S34857) for CellGro vs NK MACS experiments or 7-AAD (1:1000 diluted, Sigma, #A9400) for GMP validation runs. Cells were acquired on the Gallios (CellGro vs NK MACS) or Navios (GMP validation runs) flowcytometers and analyzed using Kaluza V2.1.3.
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3

Multicolor Flow Cytometry Panel

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The following monoclonal antibodies were used in the study: CD14-Horizon-V500, CD19-Horizon-V500 (BD Biosciences), CD3-PE-Cy5, CD56-ECD, CD57-PacificBlue, NKG2A-APC (Beckman Coulter), CD4-PE-Cy5, KIR3DL1-Alexa700 (Biolegend), KIR2DL1-biotin, KIR2DL3-FITC, NKG2C-PE (RnD systems), Aqua Dead Cell Stain Kit 405 nm, Strepavidin-Qdot-605, and Qdot-700 (Thermofisher).
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4

Multiparametric Flow Cytometry Profiling

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Mouse anti-human staining antibodies used are as follows: CD3-BrilliantUltraViolet TM (BUV)395, CD8-BUV496, CD56-BUV563, CD4-BUV661, ICOS-BUV737, CD45-BUV805, CD39-BV480, TIM-3-BrilliantBlue TM (BB)515, CD25-BB700, CD28-APC-R700 (all Becton Dickinson); CTLA-4-BrilliantViolet TM (BV)421, CD16-BV570, OX40-BV605, PD-1-BV650, CD137-BV711, CD226-BV785 (all Biolegend); NKG2A-APC (Beckman Coulter). Human anti-human GITR clone A18 (AstraZeneca Ltd, see [22] for details) was labelled using SiteClick TM sDIBO R-PE according to manufacturer's instructions (Invitrogen). CD14-, CD19-and CD20-APC-eFluor780 were used in combination with Far-Red Fixable live/dead cell stain (all eBioscience) to simultaneously remove dead cells, B cells, monocytes and CD14 + dendritic cells. See Table 2 for further details of flow cytometry antibodies used in this study.
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