Skip to main content
. 2014 Aug 21;9(8):e103725. doi: 10.1371/journal.pone.0103725

Figure 4. Presence of CD4+CD45RO+ T cells in the DC-CD4+CD45RA+ T cell co-culture influences Th1 read-out parameters.

Figure 4

(A) CD4+, CD4+CD45RO+, CD4+CD45RA+ populations have been isolated by negative immunomagnetic separation from freshly isolated PBMC. IFN-γ production of total CD4+ (black square), CD4+CD45RA+ (light gray circle), and CD4+CD45RO+ (dark gray triangle) T cells co-cultured with FMKp/IFN-γ-matured DC for 7 days as measured by CBA. (B) Contribution of contaminating CD4+CD45RO+ T cells (2.5, 5 or 10%) to CD4+CD45RA+-derived IFN-γ-production compared with pure (>99.9%) CD4+CD45RA+ T cell populations. Data shown are representative of 2 independent experiments.