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  1. 原著論文

Negligible immunogenicity of terminally differentiated cells derived from induced pluripotent or embryonic stem cells.

https://repo.qst.go.jp/records/47311
https://repo.qst.go.jp/records/47311
9c734306-f767-41f1-a315-aff5428433f7
Item type 学術雑誌論文 / Journal Article(1)
公開日 2015-09-28
タイトル
タイトル Negligible immunogenicity of terminally differentiated cells derived from induced pluripotent or embryonic stem cells.
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Araki, Ryoko

× Araki, Ryoko

WEKO 473254

Araki, Ryoko

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Uda, Masahiro

× Uda, Masahiro

WEKO 473255

Uda, Masahiro

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Hoki, Yuko

× Hoki, Yuko

WEKO 473256

Hoki, Yuko

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Sunayama, Misato

× Sunayama, Misato

WEKO 473257

Sunayama, Misato

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Nakamura, Miki

× Nakamura, Miki

WEKO 473258

Nakamura, Miki

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Ando, Shunsuke

× Ando, Shunsuke

WEKO 473259

Ando, Shunsuke

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Sugiura, Mayumi

× Sugiura, Mayumi

WEKO 473260

Sugiura, Mayumi

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Ideno, Hisashi

× Ideno, Hisashi

WEKO 473261

Ideno, Hisashi

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Shimada, Akemi

× Shimada, Akemi

WEKO 473262

Shimada, Akemi

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Nifuji, Akira

× Nifuji, Akira

WEKO 473263

Nifuji, Akira

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Abe, Masumi

× Abe, Masumi

WEKO 473264

Abe, Masumi

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荒木 良子

× 荒木 良子

WEKO 473265

en 荒木 良子

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宇田 昌広

× 宇田 昌広

WEKO 473266

en 宇田 昌広

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藤森 ゆう子

× 藤森 ゆう子

WEKO 473267

en 藤森 ゆう子

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砂山 美里

× 砂山 美里

WEKO 473268

en 砂山 美里

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中村 美樹

× 中村 美樹

WEKO 473269

en 中村 美樹

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杉浦 真由美

× 杉浦 真由美

WEKO 473270

en 杉浦 真由美

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出野 尚

× 出野 尚

WEKO 473271

en 出野 尚

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二藤 彰

× 二藤 彰

WEKO 473272

en 二藤 彰

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安倍 真澄

× 安倍 真澄

WEKO 473273

en 安倍 真澄

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抄録
内容記述タイプ Abstract
内容記述 The advantages of using induced pluripotent stem cells (iPSCs) instead of embryonic stem (ES) cells in regenerative medicine centre around circumventing concerns about the ethics of using ES cells and the likelihood of immune rejection of ES-cell-derived tissues. However, partial reprogramming and genetic instabilities in iPSCs could elicit immune responses in transplant recipients even when iPSC-derived differentiated cells are transplanted. iPSCs are first differentiated into specific types of cells in vitro for subsequent transplantation. Although model transplantation experiments have been conducted using various iPSC-derived differentiated tissues and immune rejections have not been observed, careful investigation of the immunogenicity of iPSC-derived tissue is becoming increasingly critical, especially as this has not been the focus of most studies done so far. A recent study reported immunogenicity of iPSC- but not ES-cell-derived teratomas and implicated several causative genes. Nevertheless, some controversy has arisen regarding these findings. Here we examine the immunogenicity of differentiated skin and bone marrow tissues derived from mouse iPSCs. To ensure optimal comparison of iPSCs and ES cells, we established ten integration-free iPSC and seven ES-cell lines using an inbred mouse strain, C57BL/6. We observed no differences in the rate of success of transplantation when skin and bone marrow cells derived from iPSCs were compared with ES-cell-derived tissues. Moreover, we observed limited or no immune responses, including T-cell infiltration, for tissues derived from either iPSCs or ES cells, and no increase in the expression of the immunogenicity-causing Zg16 and Hormad1 genes in regressing skin and teratoma tissues. Our findings suggest limited immunogenicity of transplanted cells differentiated from iPSCs and ES cells.
書誌情報 Nature

巻 494, 号 7435, p. 100-4, 発行日 2013-02
出版者
出版者 Nature Publishing Group
ISSN
収録物識別子タイプ ISSN
収録物識別子 0028-0836
PubMed番号
識別子タイプ PMID
関連識別子 23302801
DOI
識別子タイプ DOI
関連識別子 10.1038/nature11807
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