Fig. 6.
Fig. 6. CD34+-derived int-DCs efficiently capture antigen. / (A) May-Grünwald-Giemsa staining and anti–HLA DR labeling (revealed in DAB) of cytospun CD34+-derived int-DCs (panels Ai and Aii, original magnification, × 400). CD34+-derived int-DCs were incubated for 2 hours with heat-killed yeast and then thoroughly washed. Compare with CD34+-derived int-DCs in culture without yeast (panels Aiii and Aiv, original magnification, × 350). (B) Myc409, a recombinant Mycobacterium bovis BCG strain expressing GFP, was added for 4 hours to CD34+-derived int-DCs at an MOI of 1 or 10. Capture of Myc409 was measured by flow cytometry. The data are representative of 2 independent experiments.

CD34+-derived int-DCs efficiently capture antigen.

(A) May-Grünwald-Giemsa staining and anti–HLA DR labeling (revealed in DAB) of cytospun CD34+-derived int-DCs (panels Ai and Aii, original magnification, × 400). CD34+-derived int-DCs were incubated for 2 hours with heat-killed yeast and then thoroughly washed. Compare with CD34+-derived int-DCs in culture without yeast (panels Aiii and Aiv, original magnification, × 350). (B) Myc409, a recombinant Mycobacterium bovis BCG strain expressing GFP, was added for 4 hours to CD34+-derived int-DCs at an MOI of 1 or 10. Capture of Myc409 was measured by flow cytometry. The data are representative of 2 independent experiments.

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