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Previously, we showed that PD-L silenced DCs augment expansion of MiHA-specific CD8+ effector memory cells from transplanted patients [ 11, 12].
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Though MiHA-specific CD8+ T cells could be expanded by control DCs, the use of PD-L silenced DCs strongly augmented the expansion of MiHA-specific CD8+ T cells within 2 weeks of culture (Fig. 1e).
Either by using blocking antibodies against PD-1 or PD-L1 [ 10] or by silencing the inhibitory ligands PD-L1 and PD-L2 on DCs, which results in more stimulatory DCs, we augmented the expansion of MiHA-specific CD8+ T cells of allo-SCT patients in vitro.
The aim of this study was to determine if a single exercise bout would augment the ex vivo expansion and function of γ−δ T-cells using a clinical grade protocol designed to preferentially expand the Vdelta2 subtype.
In contrast, IL-7 treatment of aged mice did not augment thymopoiesis, nor induce expansion of splenic T cells.
Therefore, we believe that PD-L silenced DCs are a safer way to interfere with the PD-1/PD-L pathway in the allo-SCT setting, and thereby potently augment the activation and expansion of MiHA-specific CD8+ T cells.
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