Abstract
In this issue of Cell Stem Cell, Petrillo etal. (2018) improve lentiviral transduction of hematopoietic stem cells (HSCs) by using cyclosporine H to relieve viral entry restriction by interferon-induced transmembrane protein 3 (IFITM3). This finding promises to enhance the efficiency of exvivo therapeutic gene transfer and gene editing of HSCs.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have