Analysis of CD8+ TN, TCM, and TEM subsets during intermittent IL-15 administration. (A) Samples of PBMCs were obtained from macaques 97067, K00043, 02279, M05118, and T02392 before, during, and after the treatment with IL-15. Cells were stained with mAbs binding to CD3, CD8, or CD95, and CCR7 and analyzed by flow cytometry to distinguish TN (CD95lowCCR7+), TCM (CD95+CCR7+), and TEM (CD95+CCR7−) subsets. The fold increase of each subset at the indicated time of treatment is shown. The vertical bar represents the mean. indicates the duration of the IL-15 treatment. The last posttreatment PBMC sample from K00043 was obtained on day 283. (B-C) Expression of Ki-67 by CD8+ T-cell subsets. (B) Representative data of macaque 02279. Gating of CD8+ TN, TCM, and TEM subsets stained for Ki-67 expression. PBMCs were stained with mAb specific for CD3, CD8, CD95, and CCR7, permeabilized, and stained with an antibody that binds to Ki-67, and analyzed by flow cytometry. Cells are gated on CD3+CD8+ T cells. The inset value in the upper right quadrant indicates the proportion of Ki-67+ T cells (in percentage). (C) The percentage (%) of Ki-67+ T cells within the CD8+ TN, TCM, and TEM subsets is shown at the indicated time of IL-15 treatment of macaques 97067, K00043, 02279, M05118, and T02392. The vertical bar represents the mean. indicates the duration of the IL-15 treatment.