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. 2006 Dec 1;119(4):441–450. doi: 10.1111/j.1365-2567.2006.02455.x

Figure 1.

Figure 1

In vitro proliferation of Treg and Tconv cells after stimulation with the CD28-SA mAb JJ316 in the presence of different amounts of rhIL-2. (a)[3H]thymidine incorporation by 104 freshly purified Treg cells (black bars) or Tconv cells (white bars) stimulated for 3 days with the indicated amounts of CD28-SA JJ316 and rhIL-2. The bars indicate means of triplicate cultures ± SD. (b) CFSE-labelled Treg cells (left) and CFSE-labelled Tconv cells (right) were cultured for 3 days together with irradiated splenic APCs in the presence (black line) or absence (grey shadow) of the CD28-SA added in solution.