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The short and sweet of T-cell therapy

Restraining glycolysis enhances the formation of immunological memory and antitumor immune responses

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Article: e27573 | Received 13 Dec 2013, Accepted 18 Dec 2013, Published online: 03 Jan 2014

Figures & data

Figure 1. Glycolytic metabolism regulates CD8+ T-cell differentiation and effector functions. Upon antigen stimulation, naïve CD8+ T cells undergo massive clonal expansion and differentiate into effector and memory cells. This process is accompanied by metabolic alterations, including an increased flux via aerobic glycolysis. High levels of glycolysis drive CD8+ T cells toward a terminally differentiated effector state that is associated with an impaired antineoplastic activity. Inhibiting glycolysis with 2-deoxyglucose (2-DG) favors the formation of long-lived memory CD8+ T cells that mediate enhanced antitumor responses after adoptive transfer.

Figure 1. Glycolytic metabolism regulates CD8+ T-cell differentiation and effector functions. Upon antigen stimulation, naïve CD8+ T cells undergo massive clonal expansion and differentiate into effector and memory cells. This process is accompanied by metabolic alterations, including an increased flux via aerobic glycolysis. High levels of glycolysis drive CD8+ T cells toward a terminally differentiated effector state that is associated with an impaired antineoplastic activity. Inhibiting glycolysis with 2-deoxyglucose (2-DG) favors the formation of long-lived memory CD8+ T cells that mediate enhanced antitumor responses after adoptive transfer.