Abstract
The rescue of exhausted CD8+ cytolytic T-cells (CTLs) by anti-programmed cell death-1 (anti-PD-1) immune checkpoint blockade has been found to require CD28 expression. At the same time, we have shown that the inactivation of the serine/threonine kinase glycogen synthase kinase (GSK)-3α/β with small-interfering RNAs (siRNAs) and small molecule inhibitors (SMIs) specifically down-regulates PD-1 expression for enhanced CD8+ CTL function and clearance of tumors and viral infections (Taylor et al., 2016 Immunity, 44(2):274-86, Taylor et al., 2017 Cancer Research, canres.0491.2017). It has been unclear whether the GSK-3α/β pathway accounts for CD28 costimulation of CD8+ CTL function. In this presentation, we show for the first time that the inactivation of GSK-3α/β through siRNA or by SMIs during priming can substitute CD28 co-stimulation in the potentiation of cytotoxic CD8+ CTL function against the EL-4 lymphoma cells expressing OVA peptide. The effect was seen using several structurally distinct GSK-3 SMIs and was accompanied by an increase in Lamp-1 and GZMB expression. Conversely, CD28 crosslinking obviated the need for GSK-3α/β inhibition in its enhancement of CTL function. Our findings support a model where GSK-3 is the central co-signal for CD28 priming of CD8+ CTLs in anti-PD-1 immunotherapy. Anti-PD-1 and GSK-3 SMIs cooperate synergistically to limit the growth of solid melanoma tumors in mice. We will present data on the altered nature of tumor-infiltrating lymphocytes (TILs) in response to anti-PD-1 versus GSK-3 blockade and combination therapy. Our findings outline a next-generation approach using small molecule inhibitors in combination with check-point blockade therapy for the elimination of tumors.