| Literature DB >> 30827508 |
Marina Okada1, Yoshitaka Tada2, Tomohisa Seki1, Shugo Tohyama3, Jun Fujita1, Toshihiro Suzuki2, Manami Shimomura2, Kazuya Ofuji2, Yoshikazu Kishino1, Kazuaki Nakajima1, Sho Tanosaki1, Shota Someya1, Hideaki Kanazawa1, Satoru Senju4, Tetsuya Nakatsura5, Keiichi Fukuda6.
Abstract
Immunogenicity of immature pluripotent stem cells is a topic of intense debate. Immunogenic antigens, which are specific in pluripotent states, have not been described previously. In this study, we identified glypican-3 (GPC3), a known carcinoembryonic antigen, as a pluripotent state-specific immunogenic antigen. Additionally, we validated the applicability of human leukocyte antigen (HLA)-class I-restricted GPC3-reactive cytotoxic T lymphocytes (CTLs) in the removal of undifferentiated pluripotent stem cells (PSCs) from human induced pluripotent stem cell (hiPSC)-derivatives. HiPSCs uniquely express GPC3 in pluripotent states and were rejected by GPC3-reactive CTLs, which were sensitized with HLA-class I-restricted GPC3 peptides. Furthermore, GPC3-reactive CTLs selectively removed undifferentiated PSCs from hiPSC-derivatives in vitro and inhibited tumor formation in vivo. Our results demonstrate that GPC3 works as a pluripotent state-specific immunogenic antigen in hiPSCs and is applicable to regenerative medicine as a method of removing undifferentiated PSCs, which are the main cause of tumor formation.Entities:
Keywords: Cytotoxic T lymphocytes; Glypican-3; Immunotherapy; Induced pluripotent stem cell; Regenerative medicine; Tumor formation
Year: 2019 PMID: 30827508 DOI: 10.1016/j.bbrc.2019.02.094
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575