Figure 1.
Figure 1. Phenotypic and functional mapping of the CD2 antigen on pDCs. CD14+ Mx's were enriched from PBMCs by negative selection and were negative for CD3, CD19, and CD56. The remaining population was more than 93% positive for CD14 (A-D). The Mx cells were further stained with anti-T111 (A), anti-T112 (B), or anti-T113 (C-D) mAbs. Mx's (▴) and CD3+ T cells (•) were incubated sequentially with anti-T112, anti-T113, and goat antimouse mAbs (E), and changes in intracellular Ca2+ were measured. Time represents (1) the addition of T112, (2) the addition of anti-T113, (3) the addition of goat antimouse IgG, and (4) the addition of A23187 Ca2+ ionophore. The results are representative of 3 experiments.

Phenotypic and functional mapping of the CD2 antigen on pDCs. CD14+ Mx's were enriched from PBMCs by negative selection and were negative for CD3, CD19, and CD56. The remaining population was more than 93% positive for CD14 (A-D). The Mx cells were further stained with anti-T111 (A), anti-T112 (B), or anti-T113 (C-D) mAbs. Mx's (▴) and CD3+ T cells (•) were incubated sequentially with anti-T112, anti-T113, and goat antimouse mAbs (E), and changes in intracellular Ca2+ were measured. Time represents (1) the addition of T112, (2) the addition of anti-T113, (3) the addition of goat antimouse IgG, and (4) the addition of A23187 Ca2+ ionophore. The results are representative of 3 experiments.

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