TY - JOUR
T1 - Efficient production of human neutrophils from iPSCs that prevent murine lethal infection with immune cell recruitment
AU - Miyauchi, Masashi
AU - Ito, Yusuke
AU - Nakahara, Fumio
AU - Hino, Toshiya
AU - Nakamura, Fumi
AU - Iwasaki, Yuki
AU - Kawagoshi, Taiki
AU - Koya, Junji
AU - Yoshimi, Akihide
AU - Arai, Shunya
AU - Kagoya, Yuki
AU - Kurokawa, Mineo
N1 - Funding Information:
This work was funded by the Center of Innovation Program (Japan Science and Technology Agency, grant 10101519), the Japan Agency for Medical Research and Development (grant 18072499), and joint research with Kyowa Kirin Co Ltd.
Funding Information:
Conflict-of-interest disclosure: M.M., S.A., and M.K. have received research funding from Kyowa Kirin Co. Ltd. Y. Iwasaki and T.K. were employed by Kyowa Kirin Co. Ltd. while engaged in this research project. M.M., Y. Ito, and M.K. are listed as inventors on patents describing methods for generating iPSC-derived engineered neutrophils and their functions.
Funding Information:
The authors thank Chad Cowan of Harvard University for complementary DNA of CCAAT enhancer binding protein β (CEBPB); the ENCODE consortium, and the Michael Snyder laboratory at Stanford University for generating the chromatin immunoprecipitation sequencing (GSE91748); Arika Nukina-Shimura for experimental advice; Yoko Hokama, Keiko Tanaka, and Yoshiko Ito for expert technical assistance; and Kyowa Kirin Co Ltd for recombinant human G-CSF. This work was funded by the Center of Innovation Program (Japan Science and Technology Agency, grant 10101519), the Japan Agency for Medical Research and Development (grant 18072499), and joint research with Kyowa Kirin Co Ltd.
Publisher Copyright:
© 2021 American Society of Hematology
PY - 2021/12/16
Y1 - 2021/12/16
N2 - Neutrophils play an essential role in innate immune responses to bacterial and fungal infections, and loss of neutrophil function can increase the risk of acquiring lethal infections in clinical settings. Here, we show that engineered neutrophil-primed progenitors derived from human induced pluripotent stem cells can produce functional neutrophil-like cells at a clinically applicable scale that can act rapidly in vivo against lethal bacterial infections. Using 5 different mouse models, we systematically demonstrated that these neutrophil-like cells migrate to sites of inflammation and infection and increase survival against bacterial infection. In addition, we found that these human neutrophil-like cells can recruit murine immune cells. This system potentially provides a straight-forward solution for patients with neutrophil deficiency: an off-the-shelf neutrophil transfusion. This platform should facilitate the administration of human neutrophils for a broad spectrum of physiological and pathological conditions.
AB - Neutrophils play an essential role in innate immune responses to bacterial and fungal infections, and loss of neutrophil function can increase the risk of acquiring lethal infections in clinical settings. Here, we show that engineered neutrophil-primed progenitors derived from human induced pluripotent stem cells can produce functional neutrophil-like cells at a clinically applicable scale that can act rapidly in vivo against lethal bacterial infections. Using 5 different mouse models, we systematically demonstrated that these neutrophil-like cells migrate to sites of inflammation and infection and increase survival against bacterial infection. In addition, we found that these human neutrophil-like cells can recruit murine immune cells. This system potentially provides a straight-forward solution for patients with neutrophil deficiency: an off-the-shelf neutrophil transfusion. This platform should facilitate the administration of human neutrophils for a broad spectrum of physiological and pathological conditions.
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U2 - 10.1182/blood.2021011576
DO - 10.1182/blood.2021011576
M3 - Article
C2 - 34587247
AN - SCOPUS:85121237260
SN - 0006-4971
VL - 138
SP - 2555
EP - 2569
JO - Blood
JF - Blood
IS - 24
ER -