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4 protocols using cd3 pe cy7 clone 17a2

1

Quantification of Neutrophil Phagocytosis

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Recombinant MAYV E2 protein was biotinylated and conjugated to streptavidin-coated Alexa Fluor 488 beads. MAYV E2–coated beads were incubated with fivefold dilutions of antibodies (mAbs: 5–0.0016 µg/ml) in cell culture medium for 2 h at 37°C. Bone marrow cells were harvested from C57BL/6 mice. Cells were washed with PBS, and 5.0 × 104 cells per well were added to bead-antibody immune complexes and incubated for 1 h at 37°C. Cells were stained with the following antibodies: CD11b APC (clone M1/70; BioLegend), CD11c APC/Cy7 (clone N418; BioLegend), Ly6G Pacific Blue (clone 1A8; BioLegend), Ly-6C BV605 (clone HK1.4; BioLegend), and CD3 PE/Cy7 (clone 17A2; BioLegend). Cells were fixed with 4% PFA and analyzed on an IntelliCyt iQue Screener Plus flow cytometer. Neutrophils were defined as CD3 and CD11c cells that were Ly6C, CD11b+, and Ly6G+. The phagocytic score was determined using the following calculation: (percentage of Alexa Fluor 488+ cells) × (Alexa Fluor 488 geometric mean fluorescent intensity of Alexa Fluor 488+ cells)/10,000.
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2

ADNP Assay for CHIKV Antibody Detection

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The ADNP assay was adapted from a previous publication (47 (link)). Briefly, recombinant, biotinylated CHIKV p62-E1 protein was conjugated to streptavidin-coated Alexa Fluor 488 beads (Invitrogen) for 2 h at 37°C. After washing two times in 0.1% BSA in PBS, CHIKV antigen–coated beads were incubated with hyperimmune IgG (5-fold dilutions) in cell culture medium for 2 h at 37°C to form immune complexes. Bone marrow cells were harvested from C57BL/6 mice (mADNP) or primary neutrophils were isolated from fresh ACD blood (hADNP). Cells were washed with PBS, and 5.0 × 104 cells per well were added to the immune complexes and incubated for 1 h at 37°C. The following antibodies were used to stain the cells: mADNP: CD11c APC/Cy7 (clone N418; BioLegend), CD11b APC (clone M1/70; BioLegend), Ly-6C BV605 (clone HK1.4; BioLegend), Ly6G Pacific Blue (clone 1A8; BioLegend), and CD3 PE/Cy7 (clone 17A2; BioLegend) or hADNP: CD66b Pacific Blue (clone G10F5; BioLegend). Cells were fixed with 4% PFA and analyzed on a BD LSRII flow cytometer. Neutrophils were defined as CD3 and CD11c cells that were Ly6C, CD11b+, and Ly6G+ for mouse cells or CD66b+ for human cells. The phagocytic score was calculated as follows: (percentage of Alexa Fluor 488+ cells) × (Alexa Fluor 488 geometric mean fluorescent intensity of Alexa Fluor 488+ cells)/10,000.
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Flow Cytometry Antibody Panel

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We purchased directly conjugated monoclonal antibodies for flow cytometry from Invitrogen (Waltham, MA, USA): CD4-PE, Clone GK1.5; CD11b-ef450, Clone M1/70; CD44-FITC, Clone IM7; CD45AF700, Clone 30-F11; CD206-APC, Clone MR6F3; FoxP3-ef450, Clone FJK-16S, IFN-γ-PE, Clone XMG1.2; GzmB-APC, Clone GB11; iNOS-PE, Clone CXNFT; live dead fixable dead cell stain kit, Catalogue No. L34959. BD Pharmingen (San Jose, CA, USA): CD3-AF700, Clone 17A2; CD4-Pacblue and perCPcy5.5, Clone RM4-5; CD8-FITC, perCPcy5.5, and PECY7, Clone 53-6.7; CD62L-PECY7, Clone MEL-14; H2Kd-PE, Clone 17A2; Ly6G-PE and percpcy5.5, Clone 1A8; Ly6C-APCCY7, Clone- AL-21; TNF-α PECY7, Clone MP6-XT22. Biolegend (San Diego, CA, USA): CD3-PECY7 Clone 17A2; B220-percpcy5.5, Clone RA3-6B2. R&D Systems: CCR2-APC, Clone 475301; CCL2-APC, Clone 123616. eBioscience (San Diego, CA, USA): H2Kd/Dd-ef450 Clone 34-1-25; CD4-APC, Clone GK1.5.
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4

Murine CS1 Expression Analysis

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Total bone marrow and spleen cells were collected from diseased mice, followed by red blood cell lysis to analyze CS1 expression in murine samples. The following antibodies were used: CD3-PECy7 (clone 17A2, Cat# 100219), NK1.1-APCCy7 (clone PK136, Cat# 108723), CS1-PE (clone 4G2, Cat# 152005) (all derived from Biolegend) and in house purified 3H2 idiotype (secondary step: APC-labeled anti-mouse IgG1, clone RMG1-1, Cat# 406609, Biolegend). Cells were incubated for 30 min with the required antibodies (1/100 dilution) at 4°C. After washing, the percentage of positive cells and the mean fluorescence intensity (MFI) was measured using a FACSCanto Flow Cytometer (BD Biosciences) and analyzed with FlowJo 7 software (Tree Star Inc.).
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