Standardized and flexible eight colour flow cytometry panels harmonized between different. laboratories to study human NK cell phenotype and function
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1 Standardized and flexible eight colour flow cytometry panels harmonized between different laboratories to study human NK cell phenotype and function John P Veluchamy 1,2, María Delso-Vallejo 3, Nina Kok 1, Fenna Bohme 1, Ruth Seggewiss-Bernhardt 4,5, Hans J. van der Vliet 2, Tanja D. de Gruijl 2, Volker Huppert 3 and Jan Spanholtz 1* 1 Glycostem Therapeutics, Oss, The Netherlands 2 Department of Medical Oncology, VU University Medical Cancer Center Amsterdam, De Boelelaan 1117, 1081 HV Amsterdam, The Netherlands 3 Miltenyi Biotec GmbH, Bergisch Gladbach, Germany 4 Department of Haematology and Medical Oncology, University Hospital of Wuerzburg, Wuerzburg, Germany 5 Department of Haematology and Medical Oncology, Sozialstiftung Bamberg, Bamberg, Germany Veluchamy JP and Delso-Vallejo M contributed equally to this paper. Contact information: Jan Spanholtz, Glycostem Therapeutics, Pivot Park RE1134 Kloosterstraat AB Oss, The Netherlands jan.spanholtz@glycostem.com / Tel: +31-(0) Keywords: multi-colour FACS panels, harmonization, multi-center trials, NK phenotype panel, NK function panel, cryopreservation.
2 Supplementary Fig. S1 A CD25 FMO NKp44 CD107a 99.64% 0.36% 99.32% 0.44% 99.98% 0.02% 0.23% 0.01% CD25 FMO B NKp44 FMO CD107a FMO Fully stained 69.40% 30.60% 90.01% 9.99% 15.33% 0.18% 83.61% 0.88%
3 Supplementary figure 1: Fluorescence minus one (FMO) controls for gating NK function panel receptors In case of NK cell function panel experiments, a Fluorescence Minus One (FMO) control was devised to optimize the identification of NK cell activation antigens CD25, NKp44 and CD107a under different stimulated conditions. FMO stains and a fully stained sample of NK cell stimulated with cetuximab coated A431 tumor target cells is shown in figure A and B. The FMO gate clearly indicates the negative control position.
4 Supplementary Fig. S2 Gated on PBMC Gated on Singlets Gated on CD45+ Gated on NK cells CD56brightCD163.19% CD56 bright CD56dimCD % CD56 dim CD45+CD56- Gated on NK cells 60.40% 39.60% Gated on NK cells 90.40% 9.60% 0.20% Gated on NK cells 8.09% 91.91% Gated on NK cells 45.44% 54.56% Supplementary figure 2: Gating strategy for the NK cell phenotype panel The gating procedure to analyse NK cell phenotypes from PBMC population is shown. Cells acquired were gated FSC-H/FSC-A to eliminate doublets, followed by gating on the exclusion channel (CD3/TCRγδ/CD14/CD19/SYTOX Blue) against CD45. Lymphocytes negative for exclusion channel antigens and positive for CD45 were then plotted for CD45+CD56+ cells. CD56+ NK cells were then gated to define single receptor positive cells CD56+CD16+, CD56+NKG2A+, CD56+NKG2C+, CD56+NKG2D+, CD56+KIR2D+ plots from CD56+NK cells. Further to facilitate NK subset analysis, NK cells were sub-divided into NK bright and NK dim populations based on CD56 expression and CD16 levels. CD45+CD56- cells can also be studied using this gating strategy.
5 Supplementary Fig. S3 Gated on PBMC Gated on Singlets Gated on CD45+ Gated on NK cells 12.91% CD56brightCD165.23% CD56dimCD % CD56- Gated on NK cells 22.36% Gated on NK cells 77.64% 92.51% Gated on NK cells 7.49% 1.33% 98.67% Supplementary figure 3: Gating strategy for the NK cell function panel The gating procedure to analyse NK cell functions from PBMC population is shown. Singlets were selected gating PBMC against FCS-A versus FSC-H. CD45+ cells negative for CD14, CD19 and SYTOX Blue were further gated against CD3/TCRγδ and CD56 to differentiate NK cells, T cells and CD3+CD56+ cells. CD45+CD56+ NK cells were further analysed for CD16, CD107a, NKp44 and CD25 expression. NK cells shown in this figure were stimulated with A431 + CET to show higher CD107a and lower CD16 levels. Further to facilitate NK subset analysis, NK cells were sub-divided into NK bright and NK dim populations based on CD56 expression and CD16 levels. CD45+CD56- cells can also be studied using this gating strategy.
6 Supplementary Fig. S4 Comparison of non-activated fresh versus cryopreserved NK cells NK phenotype panel (n=12) A + CET B + CET C + CET D + CET
7 Supplementary figure 4: Comparison of NK phenotype panel marker differences between fresh and cryopreserved non-activated NK cells Non-activated NK cells were stimulated with target cells (A431) alone or targets coated with cetuximab (CET). Expression levels of NKG2A (A), NKG2C (B), NKG2D (C), KIR2D (D) were compared between fresh and cryopreserved NK cells for the following conditions: i) NK only ii) and iii) + CET. Data points represent the mean of triplicate values from independent experiments from 12 PBMC donors (6 donors: BD LSRFortessa + 6 donors: MACSQuant). Statistical analysis was done using Wilcoxon test and no statistically significant differences were observed between non-activated fresh and cryopreserved NK cells.
8 Supplementary Fig. S5 Comparison of non-activated fresh versus cryopreserved NK cells NK function panel A + CET (n=12) B + CET C + CET D + CET
9 Supplementary figure 5: Comparison of NK function panel marker differences between fresh and cryopreserved non-activated NK cells The capacity of NK cells to perform natural cytotoxicity and ADCC under different NK stimulated conditions were analysed on 12 healthy donors using the NK function panel antibody mix. Expression levels of CD107a (A), CD16 (B) NKp44 (C) and CD25 (D) were compared between fresh and cryopreserved non-activated NK cells for the following conditions: i) ii) and iii) + CET. Data points represent the mean of triplicate values from independent experiments from 12 PBMC donors (6 donors: BD LSRFortessa + 6 donors: MACSQuant). Statistical analysis was done using Wilcoxon test and no statistically significant differences were observed between fresh and cryopreserved non-activated NK cells.
10 Supplementary Fig. S6 Comparison of cytokine activated fresh versus cryopreserved NK cells NK phenotype panel (n=12) A + CET B + CET C + CET D + CET
11 Supplementary figure 6: Comparison of NK phenotype panel marker differences between fresh and cryopreserved cytokine activated NK cells NK cells were activated overnight with IL-2 and IL-15 and stimulated with target cells (A431) alone or targets coated with cetuximab (CET). Expression levels of NKG2A (A), NKG2C (B), NKG2D (C), KIR2D (D) were compared between fresh and cryopreserved NK cells for the following conditions: i) ii) and iii) + CET. Data points represent the mean of triplicate values from independent experiments from 12 PBMC donors (6 donors: BD LSRFortessa + 6 donors: MACSQuant). Statistical analysis was done using Wilcoxon test and no statistically significant differences were observed between fresh and cryopreserved cytokine activated NK cells.
12 Supplementary Fig. S7 Comparison of cytokine activated fresh versus cryopreserved NK cells NK function panel A + CET (n=12) B + CET *** C + CET D + CET *
13 Supplementary figure 7: Comparison of NK function panel marker differences between fresh and cryopreserved cytokine activated NK cells The capacity of NK cells to perform natural cytotoxicity and ADCC under different NK stimulated conditions were analysed on 12 healthy donors using the NK function panel antibody mix. Expression levels of CD107a (A), CD16 (B), NKp44 and CD25 (D) were compared between fresh and cryopreserved cytokine activated NK cells for the following conditions: i) ii) and iii) + CET. Data points represent the mean of triplicate values from independent experiments from 12 PBMC donors (6 donors: BD LSRFortessa + 6 donors: MACSQuant). Statistical analysis was done using Wilcoxon test and only statistically significant differences are mentioned (*p<0.05, ***p<0.001).
14 Supplementary Fig. S8 Modified gating strategy to gate on CD56dimCD16+ NK cells A Gated on Singlets Gated on CD45+ cells Gated on NK cells 12.91% CD56dimCD % Comparison of non-activated fresh versus cryopreserved CD56dimCD16+ NK cells (n=12) B + CET Comparison of cytokine activated fresh versus cryopreserved CD56dimCD16+ NK cells C + CET ***
15 Supplementary figure 8: Paired comparison analysis of CD56dim CD16+ subset using modifed NK cell gating strategy (A) The gating procedure to analyse NK cell phenotypes from PBMC population is shown. Lymphocytes negative for exclusion channel antigens and positive for CD45 were plotted for CD45+CD56+ cells. CD56+ NK cells were sub-divided into NK bright and NK dim populations based on CD56 expression and further the CD56dimCD16+ NK cells (NK effectors) were defined by gating CD45+CD3-CD56+ NK cells against CD16. (B) CD16 levels were compared between non activated fresh and cryopreserved NK cells (C) CD16 levels were compared between cytokine activated fresh and cryopreserved NK cells. In, B and C the following conditions: i) ii) and iii) + CET were compared between fresh and cryopreserved NK cells for changes in CD56dim CD16+ marker expression. Data points represent the mean of triplicate values from independent experiments from 12 PBMC donors (6 donors: BD LSRFortessa + 6 donors: MACSQuant). Statistical analysis was done using Wilcoxon test and only statistically significant differences are mentioned (***p<0.001).
16 Supplementary Table S1 Compensation settings for BD FACSCanto II Compensation matrix - NK phenotype panel BD FACSCanto TM II VioGreen VioBlue FITC PE PerCP-Vio700 PE -Vio770 APC APC-Vio770 VioGreen VioBlue FITC PE PerCP-Vio PE-Vio APC APC-Vio Compensation matrix - NK function panel BD FACSCanto TM II VioGreen VioBlue FITC PE PerCP-Vio700 PE -Vio770 APC APC-Vio770 VioGreen VioBlue FITC PE PerCP-Vio PE-Vio APC APC-Vio
17 Supplementary Table S2 Compensation settings for BD LSRFortessa Compensation matrix - NK phenotype panel BD LSRFortessa TM VioGreen VioBlue FITC PE PerCP-Vio700 PE -Vio770 APC APC-Vio770 VioGreen VioBlue FITC PE PerCP-Vio PE-Vio APC APC-Vio Compensation matrix - NK function panel BD LSRFortessa TM VioGreen VioBlue FITC PE PerCP-Vio700 PE -Vio770 APC APC-Vio770 VioGreen VioBlue FITC PE PerCP-Vio PE-Vio APC APC-Vio
18 Supplementary Table S3 Compensation settings for MACSQuant Analyzer X Compensation matrix - NK phenotype panel MACSQuant Analyzer X VioGreen VioBlue FITC PE PerCP-Vio700 PE -Vio770 APC APC-Vio770 VioGreen VioBlue FITC PE PerCP-Vio PE-Vio APC APC-Vio Compensation matrix - NK function panel MACSQuant Analyzer X VioGreen VioBlue FITC PE PerCP-Vio700 PE -Vio770 APC APC-Vio770 VioGreen VioBlue FITC PE PerCP-Vio PE-Vio APC APC-Vio
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