“…9,10 The lentiviral vector pseudotyped with VSV-glycoprotein has a broad target cell range allowing the vector to transduce a diversity of cells, such as human hematopoietic stem cells, 11,12 rat hippocampal cells, 13,14 human macrophages, 15 rat liver and muscle cells, 16 and rat retinal cells. 17 Unlike other transplanted tissues, the cornea can be maintained in vitro for days, 18,19 allowing ex vivo transduction before transplantation. 3 The permanent genetic modification of corneal cells may benefit patients with a wide variety of corneal defects.…”