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Role of γ/δ T cells in a patient with CD4+ CD3– lymphocytosis, hypereosinophilia, and high levels of IgE  Ilan Bank, MDa,d, Avner Reshef, MDb, Miriam.

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Presentation on theme: "Role of γ/δ T cells in a patient with CD4+ CD3– lymphocytosis, hypereosinophilia, and high levels of IgE  Ilan Bank, MDa,d, Avner Reshef, MDb, Miriam."— Presentation transcript:

1 Role of γ/δ T cells in a patient with CD4+ CD3– lymphocytosis, hypereosinophilia, and high levels of IgE  Ilan Bank, MDa,d, Avner Reshef, MDb, Miriam Beniaminov, MScc, Ester Rosenthal, BScc, Gideon Rechavi, MD, PhDc, Yehudit Monselise, PhDe  Journal of Allergy and Clinical Immunology  Volume 102, Issue 4, Pages (October 1998) DOI: /S (98) Copyright © 1998 Mosby, Inc. Terms and Conditions

2 Fig. 1 Representative FACS analysis of patient and normal PBMCs (0.5 × 106 ). Patient and control PBMCs were stained with mAb OKT4, OKT3, and OKT8 to respective surface antigens. y-axis is proportional to number of cells, x-axis to logarithmic of the fluorescence intensity (arbitrary units). Numbers indicate percentage of positive cells after subtraction of background control, consisting of staining with second antibody alone (FITC-conjugated goat anti-mouse Ig). Preliminary experiments determined that isotype control mAb gave no staining above background. Journal of Allergy and Clinical Immunology  , DOI: ( /S (98) ) Copyright © 1998 Mosby, Inc. Terms and Conditions

3 Fig. 2 Detection of CD4+ CD3– T cells in patient PBMCs. Patient and normal PBMCs (from 3 of the patient’s children) were stained simultaneously with anti-CD4 conjugated with PE (vertical axis) and anti-CD3 conjugated with FITC (horizontal axis). Numbers show percentage of CD4+ CD3– , CD4+ CD3+ , and CD3+ CD4– subsets in left upper, right upper, and right lower quadrants, respectively. Staining with matching negative controls (irrelevant murine Ig) conjugated with respective dyes yielded homogeneous population of cells clustering in left lower quadrant (not shown). Journal of Allergy and Clinical Immunology  , DOI: ( /S (98) ) Copyright © 1998 Mosby, Inc. Terms and Conditions

4 Fig. 3 Intracellular CD3 in PBMCs. Cytocentrifuged, acetone-fixed PBMCs from patient (P) and normal (N) individual were stained with mAb to CD3 and photomicrographed (×400). Only a small number of patient cells (approximately 15% per high power field) are strongly stained in a manner resembling that of normal lymphocytes, but weak perinuclear intracytoplasmic staining of many of the patient’s cells (approximately 80% of cells per high power field) is noted. Journal of Allergy and Clinical Immunology  , DOI: ( /S (98) ) Copyright © 1998 Mosby, Inc. Terms and Conditions

5 Fig. 4 Cytokine production by PBMCs. IFN-γ and IL-4 (pg/mL) measured by ELISA in supernatant of 2 × 106 patient and normal control (n = 7) fresh PBMCs cultured for 48 hours in 2 mL medium alone (resting) or medium containing 10 ng/mL PMA and 0.5 μg/mL of A2318 calcium ionophore (Sigma) (activated). Bars represent mean ± 1 SD of measured concentrations. Journal of Allergy and Clinical Immunology  , DOI: ( /S (98) ) Copyright © 1998 Mosby, Inc. Terms and Conditions

6 Fig. 5 T-cell subsets in cultures of patient pbmcs in experiment 1. T cells were removed from wells containing patient PBMCS after culture in medium plus il-2 for time periods indicated on abscissa. Percentage of cells expressing each indicated surface antigen was recorded after FACS analysis of cells labeled with mAbs OKT4, OKT3, and OKT8 to corresponding antigens indicated in A and with mAbs BMA031 (anti-TCRαβ), TCRδ1(anti-TCRγδ), A13 (anti-Vδ1), and BB3 (anti-Vδ2) to respective antigens indicated in B. Four-week culture was stained only with TCRδ1 and BMA031. Journal of Allergy and Clinical Immunology  , DOI: ( /S (98) ) Copyright © 1998 Mosby, Inc. Terms and Conditions

7 Fig. 6 Antigens expressed on selected cell lines from patient’s cultured T cells. Representative FACS analysis of A, CD4– CD3+ TCRγδ+ T cells derived in experiment 1; B, CD4+ CD3– cells, derived in experiment 2; C representative γδ clone (clone B7C, see Table II) derived from experiment-1 culture. Journal of Allergy and Clinical Immunology  , DOI: ( /S (98) ) Copyright © 1998 Mosby, Inc. Terms and Conditions

8 Fig. 7 IL-4 and IFN-γ production by cultured T cells. A4B, B7C, and AB12 γδ clones and CD4+ CD3– ex-2 cells were removed from 24-well tissue culture plates in which they were maintained in IL-2 containing medium and washed; 0.5 × 106 cells were placed in plastic tubes in 0.5 mL of fresh FM alone (white bars) or in fresh FM containing 10 ng/mL PMA and 0.5 μg/mL of A2318 calcium ionophore (Sigma) (black bars). Concentration of cytokines in cell-free supernatants was measured after 48 hours of culture. Bars represent mean ± 1 SD of triplicate cultures. Journal of Allergy and Clinical Immunology  , DOI: ( /S (98) ) Copyright © 1998 Mosby, Inc. Terms and Conditions

9 Fig. 8 Cytotoxicity assays. A, Killing of 51 Cr-labeled cells of K562 line. Specific cytotoxicity in 4-hour killing assays by B7C, A6A, and AB12 γδ clones and by experiment-2 line as indicated in diagrams. Results are means of triplicate experiments at indicated killer/target ratios. B, Specific cytotoxicity of γδ T-cell clones and of experiment-2 cells as indicated within each diagram against autologous (black squares) and allogeneic (white squares) LCL. *Results in which mean experimental 51 Cr release is greater than 3 SD above mean of spontaneous release.32 Journal of Allergy and Clinical Immunology  , DOI: ( /S (98) ) Copyright © 1998 Mosby, Inc. Terms and Conditions

10 Fig. 9 Ig production effect of γδ T cells. A, Concentrations of IgE in cell-free supernatants of 4 × 106 freshly isolated patient PBMCs cultured in 2 mL FM plus PWM (1:100) for 8 days alone or were cocultured with increasing numbers of the CD4+ CD3– experiment-2 cells or CD3+ TCRγδ+ experiment-1 T cells depicted in Fig 6, A and B. Results are given as mean ± 1 SD of triplicate (for 0 cells added) or mean of duplicate experiments. *Statistically significant difference (P < .05, z test) compared with mean in the absence of added cells. B, PBMCs (1 × 106 cells per culture in 1 mL of FM plus 1:100 dilution of PWM) were cultured for 8 days alone or with 1 × 106 cells of A6A Vδ1+ TCRγδ+ clone (Table II). IgE (IU/mL, y-axis on right) and IgG (mg/mL, y-axis on left) were measured in cell-free supernatant after 8 days of culture. Bars indicate mean ± 1 SD of concentrations of Ig. Journal of Allergy and Clinical Immunology  , DOI: ( /S (98) ) Copyright © 1998 Mosby, Inc. Terms and Conditions

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