<p>(A) Representative histograms for cell surface antigen expression on PHA activated CD8 Treg (CD56<sup>pos</sup>) and CD8 Tcon (CD56<sup>neg</sup>). CD56<sup>pos</sup> and CD56<sup>neg</sup> cells isolated from PBMC were stimulated with PHA and cultured in the presence of feeder cells for 8 days before being analyzed for cell surface marker expression as described in Materials and Methods. Data shown are from one of 5 representative healthy donors. (B) Activated CD56<sup>pos</sup> cells maintained high expression of CD56 and CD94 and lower expression of CD62L and CD27. CD8 Treg (CD56<sup>pos</sup>) and CD8 Tcon (CD56<sup>neg</sup>) cells isolated from PBMC were stimulated with PHA and cultured in the presence of feeder cells for 9 to 16 d...
<p><b>A</b>) Analysis of NKG2D expression on CD3<b><sup>+</sup></b>CD4<b><sup>+</sup></b> and CD3<b>...
<p>(A) Profiles of representative TIL cultures (specimen M27, TIL cultures 2 and 8) stained for CD3,...
<p>Flight (solid square) or ground AEM control (open circle) splenocytes were cultured in DMEM with ...
<p>PBMC isolated from healthy donors were stained and analyzed as described in Materials and Methods...
<p><b> </b> PBMC isolated from healthy donors (n = 5) were stained and analyzed as described in Mate...
<p>(A) Morphology of CD161<sup>−</sup>CD56<sup>+</sup> CD8 Treg. PBMC were stained as described in M...
<p>(A) Suppression of activated allogeneic clonal CD4 T cells by CD8 Treg (CD56<sup>pos</sup>) cells...
<p>Flow cytometric analyses of CD8 Treg cells (CD8+CD25hi+) from a MM patient (A) and a healthy dono...
<p>(A) Existence of CD161<sup>−</sup>CD56<sup>+</sup> CD8 T cell subset in normal PBMC. Flow cytomet...
Conversion of B cells to the CD8+ phenotype was measured by FACS analysis of in vitro PBMC cultures ...
<p>CD8<sup>+</sup> T cells freshly isolated from healthy volunteers (<i>A</i>) or after <i>in vitro<...
<p>A2-ILI tetramer+ CD8 T cells were co-stained with anti-CD45RA, CCR7, CD27, CD28, granzyme B, gran...
<p>T cells from seven donors were transfected with the vectors Scr-Vec-GFP(−) (black bars) or Scr-Ve...
<p>CD4 T cells were labeled with CFSE and co-cultured with CD8 Treg cells in different ratios (1∶1, ...
<p>Left hand panels in A–B show CD4<sup>+</sup> T cells and right hand panels show CD8<sup>+</sup> T...
<p><b>A</b>) Analysis of NKG2D expression on CD3<b><sup>+</sup></b>CD4<b><sup>+</sup></b> and CD3<b>...
<p>(A) Profiles of representative TIL cultures (specimen M27, TIL cultures 2 and 8) stained for CD3,...
<p>Flight (solid square) or ground AEM control (open circle) splenocytes were cultured in DMEM with ...
<p>PBMC isolated from healthy donors were stained and analyzed as described in Materials and Methods...
<p><b> </b> PBMC isolated from healthy donors (n = 5) were stained and analyzed as described in Mate...
<p>(A) Morphology of CD161<sup>−</sup>CD56<sup>+</sup> CD8 Treg. PBMC were stained as described in M...
<p>(A) Suppression of activated allogeneic clonal CD4 T cells by CD8 Treg (CD56<sup>pos</sup>) cells...
<p>Flow cytometric analyses of CD8 Treg cells (CD8+CD25hi+) from a MM patient (A) and a healthy dono...
<p>(A) Existence of CD161<sup>−</sup>CD56<sup>+</sup> CD8 T cell subset in normal PBMC. Flow cytomet...
Conversion of B cells to the CD8+ phenotype was measured by FACS analysis of in vitro PBMC cultures ...
<p>CD8<sup>+</sup> T cells freshly isolated from healthy volunteers (<i>A</i>) or after <i>in vitro<...
<p>A2-ILI tetramer+ CD8 T cells were co-stained with anti-CD45RA, CCR7, CD27, CD28, granzyme B, gran...
<p>T cells from seven donors were transfected with the vectors Scr-Vec-GFP(−) (black bars) or Scr-Ve...
<p>CD4 T cells were labeled with CFSE and co-cultured with CD8 Treg cells in different ratios (1∶1, ...
<p>Left hand panels in A–B show CD4<sup>+</sup> T cells and right hand panels show CD8<sup>+</sup> T...
<p><b>A</b>) Analysis of NKG2D expression on CD3<b><sup>+</sup></b>CD4<b><sup>+</sup></b> and CD3<b>...
<p>(A) Profiles of representative TIL cultures (specimen M27, TIL cultures 2 and 8) stained for CD3,...
<p>Flight (solid square) or ground AEM control (open circle) splenocytes were cultured in DMEM with ...