“…103,113 It has been shown as early as 1995 that after nerve injury, both innate immune cells (neutrophils, macrophages and dendritic cells) and acquired immune cells (T and B cells) will be recruited to the site of injury and regulate differentiation (dedifferentiation) and axonal regeneration of Schwann cells during Waller degeneration. 112,114 Moreover, as far as the current studies are concerned, macrophages play a highly important role in peripheral nerve repair. 114,115 For example, Cattin et al 105 showed that when the sciatic nerve was severed, the hypoxic state of the injury site was specifically sensed by macrophages, which would secrete VEGF-A to induce vascular differentiation and help Schwann cells to migrate and cross the severed end (bridging action), thus inducing nerve regeneration.…”