<p>Purified PBLs were stimulated for 12 days with CD3/CD28 beads. After 12 days, beads were removed and the cells set up in new media. Cytokines were added in the following concentrations IL-12: 4 ng/mL, IL-15: 10 ng/mL, IL-18: 40 ng/mL, TL1A: 100 ng/mL, TL1A Ab: 1 µg/mL. Surface expression of co-receptors and activation markers CD25, CD134, CD154 and LFA-1 after 72 h. Upper panels: Gating strategy for lymphocytes. Lower panels: Co-staining for CD4 and CD134, CD154, CD25 of LFA-1, % positive cells and MFI for upper right quadrant are shown. Data are representative of results obtained with cells from three different donors.</p
<p>Peripheral blood CD4<sup>+</sup> T cells were stimulated with anti-CD3 and anti-CD28 antibodies f...
<p>A. FACS analyses of CD86 or PD-L1 on MoLCs, dark gray, or isotype-controls, light gray. Numbers d...
<p>(A) Freshly purified PBLs stained for CD4, CD8, CD3, HLA-DR, CD16, CD56. Depletion controls for P...
<p>A. Purified PBLs were stimulated for 12 days with CD3/CD28 beads, after which cells were stimulat...
<p>Purified PBLs were stimulated for 12 days with CD3/CD28 beads. After 12 days, beads were removed ...
<p>Isolated CD4 and CD8 T cells were stimulated on anti-CD3 anti-CD28 coated plates in the presence ...
<p>(A) The representative histograms of one experiment on PBL from one donor are shown. PBL were not...
<p>PBMC were stimulated with either HBHA (A) or PPD (B) for 1 day (blue bars) or 5 days (green bars)...
<p>(A) PBLs were purified from healthy donors, CFSE stained and stimulated for 6 days with combinati...
<p>A. Splenocytes were stimulated with anti-CD3/anti-CD28 magnetic beads for intervals of 10 minutes...
<p>Purified CD4<sup>+</sup> and CD8<sup>+</sup> T cells were adjusted to 1–2×10<sup>5</sup> cells/we...
<p>PBMC were cultured overnight in medium alone, or stimulated with individual TLR ligands (Poly-I:C...
<p>Naïve CD3<sup>+</sup>, CD4<sup>+</sup>, or CD8<sup>+</sup> T-cell subsets were stimulated with 0....
A simple culture system devoid of antigen-presenting cells was used to examine the ability of immobi...
<p>Venous blood samples from 4 healthy donors were stimulated with SEB for 24 hours either as whole ...
<p>Peripheral blood CD4<sup>+</sup> T cells were stimulated with anti-CD3 and anti-CD28 antibodies f...
<p>A. FACS analyses of CD86 or PD-L1 on MoLCs, dark gray, or isotype-controls, light gray. Numbers d...
<p>(A) Freshly purified PBLs stained for CD4, CD8, CD3, HLA-DR, CD16, CD56. Depletion controls for P...
<p>A. Purified PBLs were stimulated for 12 days with CD3/CD28 beads, after which cells were stimulat...
<p>Purified PBLs were stimulated for 12 days with CD3/CD28 beads. After 12 days, beads were removed ...
<p>Isolated CD4 and CD8 T cells were stimulated on anti-CD3 anti-CD28 coated plates in the presence ...
<p>(A) The representative histograms of one experiment on PBL from one donor are shown. PBL were not...
<p>PBMC were stimulated with either HBHA (A) or PPD (B) for 1 day (blue bars) or 5 days (green bars)...
<p>(A) PBLs were purified from healthy donors, CFSE stained and stimulated for 6 days with combinati...
<p>A. Splenocytes were stimulated with anti-CD3/anti-CD28 magnetic beads for intervals of 10 minutes...
<p>Purified CD4<sup>+</sup> and CD8<sup>+</sup> T cells were adjusted to 1–2×10<sup>5</sup> cells/we...
<p>PBMC were cultured overnight in medium alone, or stimulated with individual TLR ligands (Poly-I:C...
<p>Naïve CD3<sup>+</sup>, CD4<sup>+</sup>, or CD8<sup>+</sup> T-cell subsets were stimulated with 0....
A simple culture system devoid of antigen-presenting cells was used to examine the ability of immobi...
<p>Venous blood samples from 4 healthy donors were stimulated with SEB for 24 hours either as whole ...
<p>Peripheral blood CD4<sup>+</sup> T cells were stimulated with anti-CD3 and anti-CD28 antibodies f...
<p>A. FACS analyses of CD86 or PD-L1 on MoLCs, dark gray, or isotype-controls, light gray. Numbers d...
<p>(A) Freshly purified PBLs stained for CD4, CD8, CD3, HLA-DR, CD16, CD56. Depletion controls for P...