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4 protocols using apc cy7 conjugated anti cd8

1

Flow Cytometry Analysis of Immune Cells

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Flow cytometric analysis was performed using blood samples collected before treatment (weeks 7–8 post-immunization) and at 2, 3, 5, 6, 7, and 8 weeks after treatment (weeks 9–10, 10–11, 13, 14, 15, and 16 post-immunization). All antibodies were purchased from BD Biosciences (San Jose, CA, USA). For analysis of T-cell populations, peripheral blood mononuclear cells (PBMCs) were stained with V500–conjugated anti-CD45 (BD Biosciences), PE-Cy7–conjugated anti-CD3, PerCP-Cy5.5–conjugated anti-CD4, APC-Cy7–conjugated anti-CD8, PE–conjugated anti-CD28, and APC–conjugated anti-CD95 antibodies. For analysis of B-cell populations, PBMCs were stained with V500–conjugated CD45, PE-Cy7–conjugated anti-CD3, FITC–conjugated anti-CD20, V450–conjugated anti-CD27, PerCP-Cy5.5–conjugated anti-CD21, PE–conjugated anti-IgD, and APC–conjugated anti-IgM antibodies. For analysis of regulatory T cells, PBMCs were stained with V500–conjugated anti-CD45, FITC–conjugated anti-CD4, PE-Cy7–conjugated anti-CD25, and PE–conjugated anti-FoxP3 antibodies. Flow cytometric analysis was carried out using a BD LSRFORTESSA cell analyzer (BD Biosciences).
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Lymphocyte Isolation from Tissues

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Lamina propria, lung and liver lymphocytes were isolated as described previously (31 (link)). Briefly, lamina propria lymphocytes from intestine were isolated using the Lamina Propria Dissociation Kit (Miltenyi Biotec) according to the manufacturer’s instructions followed by Percoll gradient centrifugation. Lungs were digested with collagenase D and lymphocytes were isolated by Percoll gradient centrifugation. Liver lymphocytes were isolated by Percoll gradient centrifugation. Single cell suspensions were treated with Gey’s solution and resuspended in PBS added with 2% BSA. Antibodies used for flow cytometric analysis were as follows. Percp-Cy5.5-conjugated anti-CD4 and anti-CD62L, APC-Cy7-conjugated anti-CD8 and anti-CD44, PE-conjugated anti-H2Kb, anti-CD62L, RORγt and anti-Foxp3, PE-Cy7- conjugated anti-IFNγ, anti-CD69, anti-CD8, anti-CD25 and anti-CD44, Alexa-647- conjugated anti-TNFα, FITC-conjugated anti-CD44, anti-CD4 and anti-H2kb, APC-conjugated anti-phos-Erk, anti-H2Kd and anti-IL-17 antibodies were purchased from BD Biosciences or eBioscience. In some experiments, cells were stained with an Aqua dead cell exclusion dye. Foxp3 staining kit was from eBioscience. Samples were applied to LSRII flow cytometer (Becton Dickinson), and data were collected and analyzed using FACSDiva software (Becton Dickinson).
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Flow Cytometry Antibodies for Mouse Immune Cell Analysis

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The following anti-mouse antibodies were obtained from BD PharMingen: PerCP-conjugated anti-CD3e (553067, 1 : 100), PE-conjugated anti-CD8 (557654, 1 : 100), PE-Cy7-conjugated anti-CD8 (552877, 1 : 100), APC-Cy7-conjugated anti-CD8 (557654, 1 : 100), PE-conjugated anti-CD90.1 (561404, 1 : 100), APC-conjugated anti-CD90.1 (557266, 1 : 100), PE-Cy7-conjugated anti-CD62L (560516, 1 : 100), APC-Cy7-conjugated CD62L (560514, 1 : 100), and APC-conjugated anti-IFN-γ (554413, 1 : 100). Biolegend: PE-conjugated anti-CD44 (103008, 1 : 100), PE-Cy7-conjugated anti-CD44 (103030, 1 : 100), PE-Cy7-conjugated anti-CD69 (104512, 1 : 100), and APC-conjugated anti-CD103 (121414, 1 : 100). Flow cytometry data were acquired with a FACS Canto II flow cytometer (BD Biosciences) and data were analyzed with Flowjo software (Tree Star).
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4

Multiparameter Flow Cytometry Analysis

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To separate live and dead cell populations, PBMCs were stained with Live/Dead fixable stain dye (Life Technologies, Carlsbad, CA, USA). Then, the cells were washed in PBS and incubated with PerCP-Cy5.5-conjugated anti-CD3 (eBioscience, San Diego, CA, USA), PE-Cy7-conjugated anti-CD4 (BD Biosciences, Franklin Lakes, NJ, USA), APC-Cy7-conjugated anti-CD8 (BD Biosciences), and V450-conjugated anti-CD25 (BD Biosciences). Following fixation and permeabilization using the FOXP3/Transcription Factor Staining Buffer Set (eBioscience), the cells were stained with Alexa647-conjugated anti-FOXP3 (BD Biosciences) and Alexa488-conjugated-IL-17A (BD Biosciences) or PE-conjugated-IL-17A (BD Biosciences). CellROX Green Oxidative Stress Reagents (Molecular Probes, Eugene, OR, USA) or MitoSOX Red Mitochondrial Superoxide Indicator (Invitrogen, Carlsbad, CA, USA) were used for ROS detection. The cells were analyzed with a FACSCantoII flow cytometer (BD Biosciences), and data were processed with FlowJo software (Tree Star, OR, USA).
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