Metabolic conditioning of CD8+ effector T cells for adoptive cell therapy

CD8 + effector T (T E ) cell proliferation and cytokine production depends on enhanced glucose metabolism. However, circulating T cells continuously adapt to glucose fluctuations caused by diet and inter-organ metabolite exchange. Here we show that transient glucose restriction (TGR) in activated CD8 + T E cells metabolically primes effector functions and enhances tumour clearance in mice. Tumour-specific TGR CD8 + T E cells co-cultured with tumour spheroids in replete conditions display enhanced effector molecule expression, and adoptive transfer of these cells in a murine lymphoma model leads to greater numbers of immunologically functional circulating donor cells and complete tumour clearance. Mechanistically, T E cells treated with TGR undergo metabolic remodelling that, after glucose re-exposure, supports enhanced glucose uptake, increased carbon allocation to the pentose phosphate pathway (PPP) and a cellular redox shift towards a more reduced state—all indicators of a more anabolic programme to support their enhanced functionality. Thus, metabolic conditioning could be used to promote efficiency of T-cell products for adoptive cellular therapy. Transient glucose restriction after the activation of CD8 + T E cells ex vivo induces metabolic remodelling that enhances effector functions and tumour clearance in mice.