“…Metabolic reprogramming can govern the function of T cells, macrophages, and DCs. Immune activation is mainly linked to a glycolysis-driven upregulation of anabolic processes, [184,185] AEA, 2-AG, THC, and CBD inhibit cytokine production [61,81,186,187] AEA and PEA stimulate phagocytosis [188,189] 2-AG, THC, and WIN55212-2 modulate ROS production [187,190] CBD induces apoptosis [191] Dendritic cells (DCs) CB1 and CB2 [43,64] AEA, THC, JWH-015, and JWH-133 inhibit inflammatory cytokine production [65,66] AEA and THC inhibit the capacity to induce Th1 and Th17 responses [65,67] THC induces apoptosis [68] THC impairs human monocyte-derived DC differentiation [192] Neutrophils CB1 and CB2 [70,193] AEA, CBD, and CB2 signalling reduce cell migration [69,70] AEA and 2-AG induce cell activation and the release of antimicrobial effectors [70,71,194] NK cells CB1 and CB2 [60] 2-AG and THC inhibit cytolytic activity [72,74] CB2 signalling reduces cell migration [74] O-1602 induces high cytolytic activity and cytokine production [49] Eosinophils CB1 and CB2 [195] 2-AG increases cell recruitment [195,196] WIN55212-2 reduces cell recruitment [197] Mast cells CB1 and CB2 [73,103,198] AEA and AEA-derived compounds inhibit cell maturation and degranulation…”