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Non-transmissible MV Vector with Segmented RNA Genome Establishes Different Types of iPSCs from Hematopoietic Cells.

Takafumi Hiramoto | Maino Tahara | Jiyuan Liao | Yasushi Soda | Yoshie Miura | Ryo Kurita | Hiroshi Hamana | Kota Inoue | Hiroshi Kohara | Shohei Miyamoto | Yasuki Hijikata | Shinji Okano | Yoshiyuki Yamaguchi | Yoshinao Oda | Kenji Ichiyanagi | Hidehiro Toh | Hiroyuki Sasaki | Hiroyuki Kishi | Akihide Ryo | Atsushi Muraguchi | Makoto Takeda | Kenzaburo Tani
Molecular therapy : the journal of the American Society of Gene Therapy | 2020

Recent advances in gene therapy technologies have enabled the treatment of congenital disorders and cancers and facilitated the development of innovative methods, including induced pluripotent stem cell (iPSC) production and genome editing. We recently developed a novel non-transmissible and non-integrating measles virus (MV) vector capable of transferring multiple genes simultaneously into a wide range of cells through the CD46 and CD150 receptors. The MV vector expresses four genes for iPSC generation and the GFP gene for a period of time sufficient to establish iPSCs from human fibroblasts as well as peripheral blood T cells. The transgenes were expressed differentially depending on their gene order in the vector. Human hematopoietic stem/progenitor cells were directly and efficiently reprogrammed to naive-like cells that could proliferate and differentiate into primed iPSCs by the same method used to establish primed iPSCs from other cell types. The novel MV vector has several advantages for establishing iPSCs and potential future applications in gene therapy.

Pubmed ID: 31677955

Associated grants

None

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