Fig. 8.
DC generated from transduced CD34+ CB cells. Bivariate dot plots of flow cytometric measurement of Nef− transduced cells (top) and Nef+ transduced cells (bottom). (A) CD4-APCy versus EGFP expression of cells at day 5, day 9, and day 14 of culture, as indicated. (B) CD4-APCy versus CD80-PE expression of cells shown in (A), gated on EGFP+ cells at day 9 and day 14 of culture, as indicated. Quadrants were set to include 99% of cells stained with isotypic controls and EGFP− cells in lower left quadrant. Figures indicate percentage of cells present in corresponding quadrants. (C) Proliferation of PBMCs seeded on irradiated sorted mature Nef− (⧫) or Nef+ (□) transduced DCs, measured by 3H-thymidine incorporation. Ratio S/R, ratio between number of DCs (stimulators, S) over number of PBMCs (responders, R); cpm, counts per minute. Points represent average of triplicate wells and error bars indicate standard deviation.

DC generated from transduced CD34+ CB cells. Bivariate dot plots of flow cytometric measurement of Nef transduced cells (top) and Nef+ transduced cells (bottom). (A) CD4-APCy versus EGFP expression of cells at day 5, day 9, and day 14 of culture, as indicated. (B) CD4-APCy versus CD80-PE expression of cells shown in (A), gated on EGFP+ cells at day 9 and day 14 of culture, as indicated. Quadrants were set to include 99% of cells stained with isotypic controls and EGFP cells in lower left quadrant. Figures indicate percentage of cells present in corresponding quadrants. (C) Proliferation of PBMCs seeded on irradiated sorted mature Nef (⧫) or Nef+ (□) transduced DCs, measured by 3H-thymidine incorporation. Ratio S/R, ratio between number of DCs (stimulators, S) over number of PBMCs (responders, R); cpm, counts per minute. Points represent average of triplicate wells and error bars indicate standard deviation.

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