
Abstract Group O D-negative blood cells are universal donors in transfusion medicine and methods for converting other blood groups into this universal donor group have been researched. However, conversion of D-positive cells into D-negative is yet to be achieved, although conversion of group A or B cells into O cells has been reported. The Rh D blood group is determined by the RHD gene, which encodes a 12-transmembrane domain protein. Here we convert Rh D-positive erythroid progenitor cells into D-negative cells using RHD -targeting transcription activator-like effector nucleases (TALENs). After transfection of TALEN-encoding plasmids, RHD -knockout clones are obtained. Erythroid-lineage cells differentiated from these knockout erythroid progenitor cells do not agglutinate in the presence of anti-D reagents and do not express D antigen, as assessed using flow cytometry. Our programmable nuclease-induced blood group conversion opens new avenues for compatible donor cell generation in transfusion medicine.
570, Erythrocytes, Induced Pluripotent Stem Cells, 610, Transfection, Article, Gene Knockout Techniques, Humans, RNA, Messenger, Rh-Hr Blood-Group System/metabolism, Erythroid Precursor Cells, Deoxyribonucleases, Rh-Hr Blood-Group System, Reverse Transcriptase Polymerase Chain Reaction, Gene Knockout Techniques/methods*, Gene Transfer Techniques*, Rh-Hr Blood-Group System/genetics*, Gene Transfer Techniques, Erythroid Precursor Cells/metabolism*, Fetal Blood, RNA, Erythrocytes/metabolism*, Deoxyribonucleases/genetics*, Messenger/metabolism*, Plasmids
570, Erythrocytes, Induced Pluripotent Stem Cells, 610, Transfection, Article, Gene Knockout Techniques, Humans, RNA, Messenger, Rh-Hr Blood-Group System/metabolism, Erythroid Precursor Cells, Deoxyribonucleases, Rh-Hr Blood-Group System, Reverse Transcriptase Polymerase Chain Reaction, Gene Knockout Techniques/methods*, Gene Transfer Techniques*, Rh-Hr Blood-Group System/genetics*, Gene Transfer Techniques, Erythroid Precursor Cells/metabolism*, Fetal Blood, RNA, Erythrocytes/metabolism*, Deoxyribonucleases/genetics*, Messenger/metabolism*, Plasmids
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