Figure 1.
Figure 1. Zoledronic acid activates in vitro Vγ9Vδ2 cells and induces subset distribution in cancer patients in vivo. (A) PBMCs were incubated in vitro with IPP (▵) or zoledronic acid (□) at the indicated final concentrations and 10 U/mL IL-2. Then, 7 days later, cells were collected and the percentage of Vγ9Vδ2+ cells within the CD3+ population was assessed. (B) Vγ9Vδ2 T-cell subsets were analyzed by 3-color fluorescence-activated cell-sorter (FACS) analysis before or after in vivo treatment with zoledronic acid. The following antibodies were used in different combinations: anti-Vδ2 fluorescein isothiocyanate (FITC, IMMU389; Coulter, Miami, FL), anti-CD27 phycoerythrin (PE) (M-T271; BD Pharmingen, San Diego, CA), and anti-CD45RA PE–cytochrome 5 (Cy5, 2H4; Coulter). Data were acquired on a FACSCalibur instrument (BD Biosciences, San Diego, CA) and analyzed using CellQuest software (BD Immunocytometry Systems, San Jose, CA). Error bars indicate standard deviation.

Zoledronic acid activates in vitro Vγ9Vδ2 cells and induces subset distribution in cancer patients in vivo. (A) PBMCs were incubated in vitro with IPP (▵) or zoledronic acid (□) at the indicated final concentrations and 10 U/mL IL-2. Then, 7 days later, cells were collected and the percentage of Vγ9Vδ2+ cells within the CD3+ population was assessed. (B) Vγ9Vδ2 T-cell subsets were analyzed by 3-color fluorescence-activated cell-sorter (FACS) analysis before or after in vivo treatment with zoledronic acid. The following antibodies were used in different combinations: anti-Vδ2 fluorescein isothiocyanate (FITC, IMMU389; Coulter, Miami, FL), anti-CD27 phycoerythrin (PE) (M-T271; BD Pharmingen, San Diego, CA), and anti-CD45RA PE–cytochrome 5 (Cy5, 2H4; Coulter). Data were acquired on a FACSCalibur instrument (BD Biosciences, San Diego, CA) and analyzed using CellQuest software (BD Immunocytometry Systems, San Jose, CA). Error bars indicate standard deviation.

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