Efficient production of human neutrophils from iPSCs that prevent murine lethal infection with immune cell recruitment

Author:

Miyauchi Masashi1,Ito Yusuke1,Nakahara Fumio1ORCID,Hino Toshiya1,Nakamura Fumi1,Iwasaki Yuki2,Kawagoshi Taiki2,Koya Junji1,Yoshimi Akihide1,Arai Shunya1ORCID,Kagoya Yuki3,Kurokawa Mineo13ORCID

Affiliation:

1. Department of Hematology and Oncology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan;

2. Research and Development, Kyowa Kirin Co Ltd, Tokyo, Japan; and

3. Department of Cell Therapy and Transplantation Medicine, The University of Tokyo Hospital, Tokyo, Japan

Abstract

Abstract 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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference55 articles.

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