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雑誌文献

臨床検査64巻7号

2020年07月発行

文献概要

今月の特集1 骨髄不全症の病態と検査

—再生不良性貧血—免疫病態

著者: 山﨑宏人1

所属機関: 1金沢大学附属病院輸血部

ページ範囲:P.734 - P.739

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●再生不良性貧血(AA)の発症にT細胞を介した免疫学的機序の関与を示唆する知見は多い.

●なかでも,“グリコシルホスファチジルイノシトール(GPI)アンカー膜蛋白が欠失した発作性夜間ヘモグロビン尿症(PNH)型血球”や“6pUPDによるヒト白血球抗原(HLA)-クラスⅠアレル欠失血球”の出現は,細胞傷害性T細胞(CTL)による免疫学的攻撃の関与を強く示唆する重要な現象である.

●炎症性サイトカインであるインターフェロン-γ(IFN-γ)も造血抑制にかかわっている.

●制御性T細胞(Treg)やmiRNAはT細胞活性化の調整にかかわっている.

参考文献

1)Solomou EE, Keyvanfar K, Young NS:T-bet, a Th1 transcription factor, is up-regulated in T cells from patients with aplastic anemia. Blood 107:3983-3991,2006
2)Alvarado LJ, Huntsman HD, Cheng H, et al:Eltrombopag maintains human hematopoietic stem and progenitor cells under inflammatory conditions mediated by IFN-γ. Blood 133:2043-2055,2019
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15)Gargiulo L, Papaioannou M, Sica M, et al:Glycosylphosphatidylinositol-specific, CD1d-restricted T cells in paroxysmal nocturnal hemoglobinuria. Blood 121:2753-2761,2013
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19)Zaimoku Y, Takamatsu H, Hosomichi K, et al:Identification of an HLA class I allele closely involved in the autoantigen presentation in acquired aplastic anemia. Blood 129:2908-2916,2017

掲載誌情報

出版社:株式会社医学書院

電子版ISSN:1882-1367

印刷版ISSN:0485-1420

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