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anti cd21 pe cy7  (Agilent technologies)


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    Structured Review

    Agilent technologies anti cd21 pe cy7
    Patients’ characteristics.
    Anti Cd21 Pe Cy7, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 95/100, based on 950 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti cd21 pe cy7/product/Agilent technologies
    Average 95 stars, based on 950 article reviews
    anti cd21 pe cy7 - by Bioz Stars, 2026-06
    95/100 stars

    Images

    1) Product Images from "The Antigen Presenting Potential of CD21 low B Cells"

    Article Title: The Antigen Presenting Potential of CD21 low B Cells

    Journal: Frontiers in Immunology

    doi: 10.3389/fimmu.2020.535784

    Patients’ characteristics.
    Figure Legend Snippet: Patients’ characteristics.

    Techniques Used:

    (A) General gating strategy for different CD21 low and CD21 pos B-cell subsets. CD19 pos B cells delineated by CD19 and CD21 were separated into naïve (a), IgM memory (IgM mem) (b), switched memory (sw mem) (c), and CD27 neg IgD neg memory (CD27 neg IgD neg mem) B cells (d) by expression of IgD and CD27. Subsequent gating on CD21 pos CD38 low-intermediate and CD21 low CD38 low B cells allowed the differentiation of CD21 pos and CD21 low B cells, respectively. (B) FACS plots showing CD21 and CD11c, FCRL5, CD95, ICAM-1, CD40 and CXCR5 in naive, IgM mem, sw mem and CD27 neg IgD neg mem B cells in one representative AI patient. (C) Graphs show the MFI of CD80, CD86 and HLA-DR in CD21 pos B-cell subpopulations of healthy donors (HD) and CD21 pos and CD21 low B-cell subsets of patients with autoimmune (AI) diseases in naïve, IgM mem, sw mem and CD27 neg IgD neg mem B cells. Statistical differences were considered significant at *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001. RA, SLE, sarcoidosis, psoriatic arthritis, and spondyloarthropathy were marked by different symbols as indicated in the legend. ns, not significant.
    Figure Legend Snippet: (A) General gating strategy for different CD21 low and CD21 pos B-cell subsets. CD19 pos B cells delineated by CD19 and CD21 were separated into naïve (a), IgM memory (IgM mem) (b), switched memory (sw mem) (c), and CD27 neg IgD neg memory (CD27 neg IgD neg mem) B cells (d) by expression of IgD and CD27. Subsequent gating on CD21 pos CD38 low-intermediate and CD21 low CD38 low B cells allowed the differentiation of CD21 pos and CD21 low B cells, respectively. (B) FACS plots showing CD21 and CD11c, FCRL5, CD95, ICAM-1, CD40 and CXCR5 in naive, IgM mem, sw mem and CD27 neg IgD neg mem B cells in one representative AI patient. (C) Graphs show the MFI of CD80, CD86 and HLA-DR in CD21 pos B-cell subpopulations of healthy donors (HD) and CD21 pos and CD21 low B-cell subsets of patients with autoimmune (AI) diseases in naïve, IgM mem, sw mem and CD27 neg IgD neg mem B cells. Statistical differences were considered significant at *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001. RA, SLE, sarcoidosis, psoriatic arthritis, and spondyloarthropathy were marked by different symbols as indicated in the legend. ns, not significant.

    Techniques Used: Expressing

    (A) Representative histogram overlays for the expression of CD80 and CD86 on naïve B cells of HD unstimulated, stimulated with SEB, CpG and in T-B co-cultures without or in the presence of SEB. (B) Histogram overlays for CD80 (upper line) and CD86 (bottom line) of naïve, IgM mem, switched mem and CD27 neg IgD neg mem CD21 pos B cells of one representative HD (black solid line) and CD21 pos (blue solid line) and CD21 low B cells (red solid line) of one representative AI patient in Staphylococcus enterotoxin B (SEB-) stimulated co-cultures with allogenic T cells and statistical analysis thereof. Differences were considered significant at *p < 0.05 and **p < 0.01. The different diseases were marked by different symbols as indicated in the legend.
    Figure Legend Snippet: (A) Representative histogram overlays for the expression of CD80 and CD86 on naïve B cells of HD unstimulated, stimulated with SEB, CpG and in T-B co-cultures without or in the presence of SEB. (B) Histogram overlays for CD80 (upper line) and CD86 (bottom line) of naïve, IgM mem, switched mem and CD27 neg IgD neg mem CD21 pos B cells of one representative HD (black solid line) and CD21 pos (blue solid line) and CD21 low B cells (red solid line) of one representative AI patient in Staphylococcus enterotoxin B (SEB-) stimulated co-cultures with allogenic T cells and statistical analysis thereof. Differences were considered significant at *p < 0.05 and **p < 0.01. The different diseases were marked by different symbols as indicated in the legend.

    Techniques Used: Expressing

    (A) Representative histogram overlay displaying CD69 expression in unstimulated T cells (T only) or T-B co-cultures with naïve CD21 pos B cells of a HD or naïve CD21 low B cells of an AI patients in the absence (T + (B) or presence of SEB (T + B + SEB) gated on naïve T cells. (B – D) Histogram overlays for CD69, CD25 and Inducible Co-stimulator (ICOS) on naïve (CD45RA pos ) CD4 T cells co-cultured with naïve, IgM mem, sw mem and CD27 neg IgD neg mem B-cell populations of CD21 pos B cells of one representative HD and CD21 pos and CD21 low populations of one representative patient and statistical analysis thereof. T cells cultured alone and with or without stimulation with SEB were obtained as control. Subsets marked in green (*) were significantly different to the SEB-stimulated T-cell control (p < 0.05). All subsets were statistically significant to unstimulated T cells. Differences were considered significant at *p < 0.05 * and **p < 0.01. The different diseases were marked by different symbols as indicated in the legend.
    Figure Legend Snippet: (A) Representative histogram overlay displaying CD69 expression in unstimulated T cells (T only) or T-B co-cultures with naïve CD21 pos B cells of a HD or naïve CD21 low B cells of an AI patients in the absence (T + (B) or presence of SEB (T + B + SEB) gated on naïve T cells. (B – D) Histogram overlays for CD69, CD25 and Inducible Co-stimulator (ICOS) on naïve (CD45RA pos ) CD4 T cells co-cultured with naïve, IgM mem, sw mem and CD27 neg IgD neg mem B-cell populations of CD21 pos B cells of one representative HD and CD21 pos and CD21 low populations of one representative patient and statistical analysis thereof. T cells cultured alone and with or without stimulation with SEB were obtained as control. Subsets marked in green (*) were significantly different to the SEB-stimulated T-cell control (p < 0.05). All subsets were statistically significant to unstimulated T cells. Differences were considered significant at *p < 0.05 * and **p < 0.01. The different diseases were marked by different symbols as indicated in the legend.

    Techniques Used: Expressing, Cell Culture

    Histogram overlays for CD69 (A) , CD25 (B) , and ICOS (C) expression on memory (CD45RA neg ) CD4 T cells co-cultured with naïve, IgM mem, sw mem and CD27 neg IgD neg mem B-cell populations of CD21 pos B cells of one representative HD and CD21 pos and CD21 low populations of one representative patient and statistical analysis thereof. T cells cultured alone and with or without stimulation with SEB were obtained as control. (D) Representative FACS plot for CD4 and PD-1 or the FMO in unstimulated T cells, T cells stimulated with SEB and T cells co-cultured with naïve CD21 pos B cells of HD or naive CD21 low B cells of a patient in the absence or presence of SEB. Graph shows the proportion of PD-1 positive memory T cells in T-cell cultures stimulated as indicated to unstimulated T cells. Subsets marked with green stars were significantly different to the SEB-stimulated T-cell controls. Differences were considered significant at *p < 0.05. The different diseases were marked by different symbols as indicated in the legend. **p < 0.01.
    Figure Legend Snippet: Histogram overlays for CD69 (A) , CD25 (B) , and ICOS (C) expression on memory (CD45RA neg ) CD4 T cells co-cultured with naïve, IgM mem, sw mem and CD27 neg IgD neg mem B-cell populations of CD21 pos B cells of one representative HD and CD21 pos and CD21 low populations of one representative patient and statistical analysis thereof. T cells cultured alone and with or without stimulation with SEB were obtained as control. (D) Representative FACS plot for CD4 and PD-1 or the FMO in unstimulated T cells, T cells stimulated with SEB and T cells co-cultured with naïve CD21 pos B cells of HD or naive CD21 low B cells of a patient in the absence or presence of SEB. Graph shows the proportion of PD-1 positive memory T cells in T-cell cultures stimulated as indicated to unstimulated T cells. Subsets marked with green stars were significantly different to the SEB-stimulated T-cell controls. Differences were considered significant at *p < 0.05. The different diseases were marked by different symbols as indicated in the legend. **p < 0.01.

    Techniques Used: Expressing, Cell Culture

    (A) Cytokines measured in supernatants of T-B co-cultures. Production of TNF-α, IL-2, IFN-γ, IL-4, and IL-10 was measured in T-B co-cultures with different B-cell subsets of AI patients and HD. Subsets marked in green were significantly different to the SEB-stimulated T-cell control. (B) Intracellular cytokine staining of TNF-α and IL-10 versus CD19 in T-B co-cultures with and without SEB and T-cell SEB control. Representative FACS Plots of co-cultures with naïve B cells of HD are displayed. Data are representative for 1–3 times for each CD21 low B-cell subpopulation of patients and 2–4 times of each CD21 pos B-cell subpopulations of HD in 4 independent experiments. Differences were considered significant at *p < 0.05 and **p < 0.01.
    Figure Legend Snippet: (A) Cytokines measured in supernatants of T-B co-cultures. Production of TNF-α, IL-2, IFN-γ, IL-4, and IL-10 was measured in T-B co-cultures with different B-cell subsets of AI patients and HD. Subsets marked in green were significantly different to the SEB-stimulated T-cell control. (B) Intracellular cytokine staining of TNF-α and IL-10 versus CD19 in T-B co-cultures with and without SEB and T-cell SEB control. Representative FACS Plots of co-cultures with naïve B cells of HD are displayed. Data are representative for 1–3 times for each CD21 low B-cell subpopulation of patients and 2–4 times of each CD21 pos B-cell subpopulations of HD in 4 independent experiments. Differences were considered significant at *p < 0.05 and **p < 0.01.

    Techniques Used: Staining



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    Image Search Results


    Representative overlapping histograms from PBL nB cells (CD19 + IgD + CD27 − ) (black), NP IgD+ B cells (CD19 + IgD + CD27 − ) (blue) and NP ASC (CD19 lo CD27 hi CD38 hi ) (red) of the following surface marker expression: CD20, CD21, CD23, CD38, CD80, CD86, CD11c, CD71, α4β7, CXCR4, and SLAMF7 and intracellular expression of IRF4, Ki-67. The number of samples analyzed for each marker and the mean MFI are shown in Supplementary Table .

    Journal: Mucosal Immunology

    Article Title: Extrafollicular IgD+ B cells generate IgE antibody secreting cells in the nasal mucosa

    doi: 10.1038/s41385-021-00410-w

    Figure Lengend Snippet: Representative overlapping histograms from PBL nB cells (CD19 + IgD + CD27 − ) (black), NP IgD+ B cells (CD19 + IgD + CD27 − ) (blue) and NP ASC (CD19 lo CD27 hi CD38 hi ) (red) of the following surface marker expression: CD20, CD21, CD23, CD38, CD80, CD86, CD11c, CD71, α4β7, CXCR4, and SLAMF7 and intracellular expression of IRF4, Ki-67. The number of samples analyzed for each marker and the mean MFI are shown in Supplementary Table .

    Article Snippet: Mononuclear cells from PBL or NP cells were incubated with normal mouse serum for 20 min, in order to saturate and block nonspecific binding sites, then stained with different combinations of the following anti-human antibodies directed against human molecules: CD3-PE-Cy5.5, CD14-PE-Cy5.5 (Invitrogen, Camarillo, CA), or CD3 BV711,CD14 BV711, CD27 APC- Alexa750, CD20 PE, CD23 Pe-Cy7, CXCR4-PE-Cy5, CD80 PE-Cy7, HLA-DR PE, CD124 PE, intracellular Ki-67-FITC, IRF4-PE, (eBioscience, BioLegend, San Diego, CA), CD19-PE-Cy7 or APC CD11C PE, IgD FITC, CD38-Pacific Blue, HLA-DR-AlexaFluor700, CD21 PE-Cy7, IgG PE or APC, IgA PE or APC, CD71 PE, CD86 PE, IgM PE or APC (BD Pharmingen, San Diego, CA), CD138-APC (Miltenyi Biotec, Aubrun, CA.).

    Techniques: Marker, Expressing

    Patients’ characteristics.

    Journal: Frontiers in Immunology

    Article Title: The Antigen Presenting Potential of CD21 low B Cells

    doi: 10.3389/fimmu.2020.535784

    Figure Lengend Snippet: Patients’ characteristics.

    Article Snippet: Anti-CD19 APC-Cy7, anti-CD38 PerCp-Cy5.5, anti-CD4 PE-Cy7, anti-CD25 PerCP-Cy5.5, anti-CD86 APC, anti-CD80 BV421, anti-CD45RA BV605, anti-ICOS PE, anti-CD21 PE-Cy7, anti-CD80 BV421, anti-CD27 PerCp-Cy5.5, anti-PD-1 APC, anti-CD45RA APC-Cy7, anti-HLA-DR BV605, anti-CD11c AF700, anti-CD86 BV711, anti-CD95 BV650, anti-IgD BV786, anti-FCRL5 APC, anti-CXCR3 BV421, anti-CCR6 BV605, anti-CD19 BV650, anti-CD19 BV605, anti-PD-L1 BV421, anti-PD-L2 PE, anti-ICOS-L PE, anti-OX40L PE, anti-IL-10 PE, anti-IL-10 APC, anti-TNF-α APC-Cy7 (all obtained from BioLegend); anti-IgD FITC and anti-IgD PE (both from Southern Biotech); anti-CD27 PE (Dako); and anti-CD21 PE-Cy7, anti-CD69 FITC, anti-HLA-DR FITC, anti-CD27 BV605, anti-CD40 FITC, anti-CD40L PE, anti-ICAM-1 PE, anti-CXCR5 BUV395 and anti-CD27 BUV395 (all from BD Biosciences).

    Techniques:

    (A) General gating strategy for different CD21 low and CD21 pos B-cell subsets. CD19 pos B cells delineated by CD19 and CD21 were separated into naïve (a), IgM memory (IgM mem) (b), switched memory (sw mem) (c), and CD27 neg IgD neg memory (CD27 neg IgD neg mem) B cells (d) by expression of IgD and CD27. Subsequent gating on CD21 pos CD38 low-intermediate and CD21 low CD38 low B cells allowed the differentiation of CD21 pos and CD21 low B cells, respectively. (B) FACS plots showing CD21 and CD11c, FCRL5, CD95, ICAM-1, CD40 and CXCR5 in naive, IgM mem, sw mem and CD27 neg IgD neg mem B cells in one representative AI patient. (C) Graphs show the MFI of CD80, CD86 and HLA-DR in CD21 pos B-cell subpopulations of healthy donors (HD) and CD21 pos and CD21 low B-cell subsets of patients with autoimmune (AI) diseases in naïve, IgM mem, sw mem and CD27 neg IgD neg mem B cells. Statistical differences were considered significant at *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001. RA, SLE, sarcoidosis, psoriatic arthritis, and spondyloarthropathy were marked by different symbols as indicated in the legend. ns, not significant.

    Journal: Frontiers in Immunology

    Article Title: The Antigen Presenting Potential of CD21 low B Cells

    doi: 10.3389/fimmu.2020.535784

    Figure Lengend Snippet: (A) General gating strategy for different CD21 low and CD21 pos B-cell subsets. CD19 pos B cells delineated by CD19 and CD21 were separated into naïve (a), IgM memory (IgM mem) (b), switched memory (sw mem) (c), and CD27 neg IgD neg memory (CD27 neg IgD neg mem) B cells (d) by expression of IgD and CD27. Subsequent gating on CD21 pos CD38 low-intermediate and CD21 low CD38 low B cells allowed the differentiation of CD21 pos and CD21 low B cells, respectively. (B) FACS plots showing CD21 and CD11c, FCRL5, CD95, ICAM-1, CD40 and CXCR5 in naive, IgM mem, sw mem and CD27 neg IgD neg mem B cells in one representative AI patient. (C) Graphs show the MFI of CD80, CD86 and HLA-DR in CD21 pos B-cell subpopulations of healthy donors (HD) and CD21 pos and CD21 low B-cell subsets of patients with autoimmune (AI) diseases in naïve, IgM mem, sw mem and CD27 neg IgD neg mem B cells. Statistical differences were considered significant at *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001. RA, SLE, sarcoidosis, psoriatic arthritis, and spondyloarthropathy were marked by different symbols as indicated in the legend. ns, not significant.

    Article Snippet: Anti-CD19 APC-Cy7, anti-CD38 PerCp-Cy5.5, anti-CD4 PE-Cy7, anti-CD25 PerCP-Cy5.5, anti-CD86 APC, anti-CD80 BV421, anti-CD45RA BV605, anti-ICOS PE, anti-CD21 PE-Cy7, anti-CD80 BV421, anti-CD27 PerCp-Cy5.5, anti-PD-1 APC, anti-CD45RA APC-Cy7, anti-HLA-DR BV605, anti-CD11c AF700, anti-CD86 BV711, anti-CD95 BV650, anti-IgD BV786, anti-FCRL5 APC, anti-CXCR3 BV421, anti-CCR6 BV605, anti-CD19 BV650, anti-CD19 BV605, anti-PD-L1 BV421, anti-PD-L2 PE, anti-ICOS-L PE, anti-OX40L PE, anti-IL-10 PE, anti-IL-10 APC, anti-TNF-α APC-Cy7 (all obtained from BioLegend); anti-IgD FITC and anti-IgD PE (both from Southern Biotech); anti-CD27 PE (Dako); and anti-CD21 PE-Cy7, anti-CD69 FITC, anti-HLA-DR FITC, anti-CD27 BV605, anti-CD40 FITC, anti-CD40L PE, anti-ICAM-1 PE, anti-CXCR5 BUV395 and anti-CD27 BUV395 (all from BD Biosciences).

    Techniques: Expressing

    (A) Representative histogram overlays for the expression of CD80 and CD86 on naïve B cells of HD unstimulated, stimulated with SEB, CpG and in T-B co-cultures without or in the presence of SEB. (B) Histogram overlays for CD80 (upper line) and CD86 (bottom line) of naïve, IgM mem, switched mem and CD27 neg IgD neg mem CD21 pos B cells of one representative HD (black solid line) and CD21 pos (blue solid line) and CD21 low B cells (red solid line) of one representative AI patient in Staphylococcus enterotoxin B (SEB-) stimulated co-cultures with allogenic T cells and statistical analysis thereof. Differences were considered significant at *p < 0.05 and **p < 0.01. The different diseases were marked by different symbols as indicated in the legend.

    Journal: Frontiers in Immunology

    Article Title: The Antigen Presenting Potential of CD21 low B Cells

    doi: 10.3389/fimmu.2020.535784

    Figure Lengend Snippet: (A) Representative histogram overlays for the expression of CD80 and CD86 on naïve B cells of HD unstimulated, stimulated with SEB, CpG and in T-B co-cultures without or in the presence of SEB. (B) Histogram overlays for CD80 (upper line) and CD86 (bottom line) of naïve, IgM mem, switched mem and CD27 neg IgD neg mem CD21 pos B cells of one representative HD (black solid line) and CD21 pos (blue solid line) and CD21 low B cells (red solid line) of one representative AI patient in Staphylococcus enterotoxin B (SEB-) stimulated co-cultures with allogenic T cells and statistical analysis thereof. Differences were considered significant at *p < 0.05 and **p < 0.01. The different diseases were marked by different symbols as indicated in the legend.

    Article Snippet: Anti-CD19 APC-Cy7, anti-CD38 PerCp-Cy5.5, anti-CD4 PE-Cy7, anti-CD25 PerCP-Cy5.5, anti-CD86 APC, anti-CD80 BV421, anti-CD45RA BV605, anti-ICOS PE, anti-CD21 PE-Cy7, anti-CD80 BV421, anti-CD27 PerCp-Cy5.5, anti-PD-1 APC, anti-CD45RA APC-Cy7, anti-HLA-DR BV605, anti-CD11c AF700, anti-CD86 BV711, anti-CD95 BV650, anti-IgD BV786, anti-FCRL5 APC, anti-CXCR3 BV421, anti-CCR6 BV605, anti-CD19 BV650, anti-CD19 BV605, anti-PD-L1 BV421, anti-PD-L2 PE, anti-ICOS-L PE, anti-OX40L PE, anti-IL-10 PE, anti-IL-10 APC, anti-TNF-α APC-Cy7 (all obtained from BioLegend); anti-IgD FITC and anti-IgD PE (both from Southern Biotech); anti-CD27 PE (Dako); and anti-CD21 PE-Cy7, anti-CD69 FITC, anti-HLA-DR FITC, anti-CD27 BV605, anti-CD40 FITC, anti-CD40L PE, anti-ICAM-1 PE, anti-CXCR5 BUV395 and anti-CD27 BUV395 (all from BD Biosciences).

    Techniques: Expressing

    (A) Representative histogram overlay displaying CD69 expression in unstimulated T cells (T only) or T-B co-cultures with naïve CD21 pos B cells of a HD or naïve CD21 low B cells of an AI patients in the absence (T + (B) or presence of SEB (T + B + SEB) gated on naïve T cells. (B – D) Histogram overlays for CD69, CD25 and Inducible Co-stimulator (ICOS) on naïve (CD45RA pos ) CD4 T cells co-cultured with naïve, IgM mem, sw mem and CD27 neg IgD neg mem B-cell populations of CD21 pos B cells of one representative HD and CD21 pos and CD21 low populations of one representative patient and statistical analysis thereof. T cells cultured alone and with or without stimulation with SEB were obtained as control. Subsets marked in green (*) were significantly different to the SEB-stimulated T-cell control (p < 0.05). All subsets were statistically significant to unstimulated T cells. Differences were considered significant at *p < 0.05 * and **p < 0.01. The different diseases were marked by different symbols as indicated in the legend.

    Journal: Frontiers in Immunology

    Article Title: The Antigen Presenting Potential of CD21 low B Cells

    doi: 10.3389/fimmu.2020.535784

    Figure Lengend Snippet: (A) Representative histogram overlay displaying CD69 expression in unstimulated T cells (T only) or T-B co-cultures with naïve CD21 pos B cells of a HD or naïve CD21 low B cells of an AI patients in the absence (T + (B) or presence of SEB (T + B + SEB) gated on naïve T cells. (B – D) Histogram overlays for CD69, CD25 and Inducible Co-stimulator (ICOS) on naïve (CD45RA pos ) CD4 T cells co-cultured with naïve, IgM mem, sw mem and CD27 neg IgD neg mem B-cell populations of CD21 pos B cells of one representative HD and CD21 pos and CD21 low populations of one representative patient and statistical analysis thereof. T cells cultured alone and with or without stimulation with SEB were obtained as control. Subsets marked in green (*) were significantly different to the SEB-stimulated T-cell control (p < 0.05). All subsets were statistically significant to unstimulated T cells. Differences were considered significant at *p < 0.05 * and **p < 0.01. The different diseases were marked by different symbols as indicated in the legend.

    Article Snippet: Anti-CD19 APC-Cy7, anti-CD38 PerCp-Cy5.5, anti-CD4 PE-Cy7, anti-CD25 PerCP-Cy5.5, anti-CD86 APC, anti-CD80 BV421, anti-CD45RA BV605, anti-ICOS PE, anti-CD21 PE-Cy7, anti-CD80 BV421, anti-CD27 PerCp-Cy5.5, anti-PD-1 APC, anti-CD45RA APC-Cy7, anti-HLA-DR BV605, anti-CD11c AF700, anti-CD86 BV711, anti-CD95 BV650, anti-IgD BV786, anti-FCRL5 APC, anti-CXCR3 BV421, anti-CCR6 BV605, anti-CD19 BV650, anti-CD19 BV605, anti-PD-L1 BV421, anti-PD-L2 PE, anti-ICOS-L PE, anti-OX40L PE, anti-IL-10 PE, anti-IL-10 APC, anti-TNF-α APC-Cy7 (all obtained from BioLegend); anti-IgD FITC and anti-IgD PE (both from Southern Biotech); anti-CD27 PE (Dako); and anti-CD21 PE-Cy7, anti-CD69 FITC, anti-HLA-DR FITC, anti-CD27 BV605, anti-CD40 FITC, anti-CD40L PE, anti-ICAM-1 PE, anti-CXCR5 BUV395 and anti-CD27 BUV395 (all from BD Biosciences).

    Techniques: Expressing, Cell Culture

    Histogram overlays for CD69 (A) , CD25 (B) , and ICOS (C) expression on memory (CD45RA neg ) CD4 T cells co-cultured with naïve, IgM mem, sw mem and CD27 neg IgD neg mem B-cell populations of CD21 pos B cells of one representative HD and CD21 pos and CD21 low populations of one representative patient and statistical analysis thereof. T cells cultured alone and with or without stimulation with SEB were obtained as control. (D) Representative FACS plot for CD4 and PD-1 or the FMO in unstimulated T cells, T cells stimulated with SEB and T cells co-cultured with naïve CD21 pos B cells of HD or naive CD21 low B cells of a patient in the absence or presence of SEB. Graph shows the proportion of PD-1 positive memory T cells in T-cell cultures stimulated as indicated to unstimulated T cells. Subsets marked with green stars were significantly different to the SEB-stimulated T-cell controls. Differences were considered significant at *p < 0.05. The different diseases were marked by different symbols as indicated in the legend. **p < 0.01.

    Journal: Frontiers in Immunology

    Article Title: The Antigen Presenting Potential of CD21 low B Cells

    doi: 10.3389/fimmu.2020.535784

    Figure Lengend Snippet: Histogram overlays for CD69 (A) , CD25 (B) , and ICOS (C) expression on memory (CD45RA neg ) CD4 T cells co-cultured with naïve, IgM mem, sw mem and CD27 neg IgD neg mem B-cell populations of CD21 pos B cells of one representative HD and CD21 pos and CD21 low populations of one representative patient and statistical analysis thereof. T cells cultured alone and with or without stimulation with SEB were obtained as control. (D) Representative FACS plot for CD4 and PD-1 or the FMO in unstimulated T cells, T cells stimulated with SEB and T cells co-cultured with naïve CD21 pos B cells of HD or naive CD21 low B cells of a patient in the absence or presence of SEB. Graph shows the proportion of PD-1 positive memory T cells in T-cell cultures stimulated as indicated to unstimulated T cells. Subsets marked with green stars were significantly different to the SEB-stimulated T-cell controls. Differences were considered significant at *p < 0.05. The different diseases were marked by different symbols as indicated in the legend. **p < 0.01.

    Article Snippet: Anti-CD19 APC-Cy7, anti-CD38 PerCp-Cy5.5, anti-CD4 PE-Cy7, anti-CD25 PerCP-Cy5.5, anti-CD86 APC, anti-CD80 BV421, anti-CD45RA BV605, anti-ICOS PE, anti-CD21 PE-Cy7, anti-CD80 BV421, anti-CD27 PerCp-Cy5.5, anti-PD-1 APC, anti-CD45RA APC-Cy7, anti-HLA-DR BV605, anti-CD11c AF700, anti-CD86 BV711, anti-CD95 BV650, anti-IgD BV786, anti-FCRL5 APC, anti-CXCR3 BV421, anti-CCR6 BV605, anti-CD19 BV650, anti-CD19 BV605, anti-PD-L1 BV421, anti-PD-L2 PE, anti-ICOS-L PE, anti-OX40L PE, anti-IL-10 PE, anti-IL-10 APC, anti-TNF-α APC-Cy7 (all obtained from BioLegend); anti-IgD FITC and anti-IgD PE (both from Southern Biotech); anti-CD27 PE (Dako); and anti-CD21 PE-Cy7, anti-CD69 FITC, anti-HLA-DR FITC, anti-CD27 BV605, anti-CD40 FITC, anti-CD40L PE, anti-ICAM-1 PE, anti-CXCR5 BUV395 and anti-CD27 BUV395 (all from BD Biosciences).

    Techniques: Expressing, Cell Culture

    (A) Cytokines measured in supernatants of T-B co-cultures. Production of TNF-α, IL-2, IFN-γ, IL-4, and IL-10 was measured in T-B co-cultures with different B-cell subsets of AI patients and HD. Subsets marked in green were significantly different to the SEB-stimulated T-cell control. (B) Intracellular cytokine staining of TNF-α and IL-10 versus CD19 in T-B co-cultures with and without SEB and T-cell SEB control. Representative FACS Plots of co-cultures with naïve B cells of HD are displayed. Data are representative for 1–3 times for each CD21 low B-cell subpopulation of patients and 2–4 times of each CD21 pos B-cell subpopulations of HD in 4 independent experiments. Differences were considered significant at *p < 0.05 and **p < 0.01.

    Journal: Frontiers in Immunology

    Article Title: The Antigen Presenting Potential of CD21 low B Cells

    doi: 10.3389/fimmu.2020.535784

    Figure Lengend Snippet: (A) Cytokines measured in supernatants of T-B co-cultures. Production of TNF-α, IL-2, IFN-γ, IL-4, and IL-10 was measured in T-B co-cultures with different B-cell subsets of AI patients and HD. Subsets marked in green were significantly different to the SEB-stimulated T-cell control. (B) Intracellular cytokine staining of TNF-α and IL-10 versus CD19 in T-B co-cultures with and without SEB and T-cell SEB control. Representative FACS Plots of co-cultures with naïve B cells of HD are displayed. Data are representative for 1–3 times for each CD21 low B-cell subpopulation of patients and 2–4 times of each CD21 pos B-cell subpopulations of HD in 4 independent experiments. Differences were considered significant at *p < 0.05 and **p < 0.01.

    Article Snippet: Anti-CD19 APC-Cy7, anti-CD38 PerCp-Cy5.5, anti-CD4 PE-Cy7, anti-CD25 PerCP-Cy5.5, anti-CD86 APC, anti-CD80 BV421, anti-CD45RA BV605, anti-ICOS PE, anti-CD21 PE-Cy7, anti-CD80 BV421, anti-CD27 PerCp-Cy5.5, anti-PD-1 APC, anti-CD45RA APC-Cy7, anti-HLA-DR BV605, anti-CD11c AF700, anti-CD86 BV711, anti-CD95 BV650, anti-IgD BV786, anti-FCRL5 APC, anti-CXCR3 BV421, anti-CCR6 BV605, anti-CD19 BV650, anti-CD19 BV605, anti-PD-L1 BV421, anti-PD-L2 PE, anti-ICOS-L PE, anti-OX40L PE, anti-IL-10 PE, anti-IL-10 APC, anti-TNF-α APC-Cy7 (all obtained from BioLegend); anti-IgD FITC and anti-IgD PE (both from Southern Biotech); anti-CD27 PE (Dako); and anti-CD21 PE-Cy7, anti-CD69 FITC, anti-HLA-DR FITC, anti-CD27 BV605, anti-CD40 FITC, anti-CD40L PE, anti-ICAM-1 PE, anti-CXCR5 BUV395 and anti-CD27 BUV395 (all from BD Biosciences).

    Techniques: Staining

    KEY RESOURCES TABLE

    Journal: Cell reports

    Article Title: Neonatal Rhesus Macaques Have Distinct Immune Cell Transcriptional Profiles following HIV Envelope Immunization

    doi: 10.1016/j.celrep.2019.12.091

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Mouse anti-Human CD21 PE-Cy7, Clone B-ly4 , BD Biosciences , Cat# 561374; RRID:AB_10681717.

    Techniques: Isolation, Negative Control, Mutagenesis, Recombinant, Software