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Mismatched human leukocyte antigen class II-restricted CD8+ cytotoxic T cells may mediate selective graft-versus-leukemia effects following allogeneic hematopoietic cell transplantation

  • Tomoya Hirosawa
  • , Hiroki Torikai
  • , Mayumi Yanagisawa
  • , Michi Kamei
  • , Nobuhiko Imahashi
  • , Ayako Demachi-Okamura
  • , Miyoko Tanimoto
  • , Keiko Shiraishi
  • , Mamoru Ito
  • , Koichi Miyamura
  • , Kiyosumi Shibata
  • , Fumitaka Kikkawa
  • , Yasuo Morishima
  • , Toshitada Takahashi
  • , Nobuhiko Emi
  • , Kiyotaka Kuzushima
  • , Yoshiki Akatsuka

研究成果: ジャーナルへの寄稿学術論文査読

7   !!Link opens in a new tab 被引用数 (Scopus)

抄録

Partial human leukocyte antigen (HLA)-mismatched hematopoietic stem cell transplantation (HSCT) is often performed when an HLA-matched donor is not available. In these cases, CD8+ or CD4+ T cell responses are induced depending on the mismatched HLA class I or II allele(s). Herein, we report on an HLA-DRB1*08:03-restricted CD8+ CTL clone, named CTL-1H8, isolated from a patient following an HLA-DR-mismatched HSCT from his brother. Lysis of a patient Epstein-Barr virus-transformed B cell line (B-LCL) by CTL-1H8 was inhibited after the addition of blocking antibodies against HLA-DR and CD8, whereas antibodies against pan-HLA class I or CD4 had no effect. The 1H8-CTL clone did not lyse the recipient dermal fibroblasts whose HLA-DRB1*08:03 expression was upregulated after 1week cytokine treatment. Engraftment of HLA-DRB1*08:03-positive primary leukemic stem cells in non-obese diabetic/severe combined immunodeficient/γc-null (NOG) mice was completely inhibited by the in vitro preincubation of cells with CTL-1H8, suggesting that HLA-DRB1*08:03 is expressed on leukemic stem cells. Finally, analysis of the precursor frequency of CD8+ CTL specific for recipient antigens in post-HSCT peripheral blood T cells revealed a significant fraction of the total donor CTL responses towards the individual mismatched HLA-DR antigen in two patients. These findings underscore unexpectedly significant CD8 T cell responses in the context of HLA class II.

本文言語英語
ページ(範囲)1281-1286
ページ数6
ジャーナルCancer science
102
7
DOI
出版ステータス出版済み - 07-2011
外部発表はい

UN SDG

この成果は、次の持続可能な開発目標に貢献しています

  1. SDG 3 - すべての人に健康と福祉を
    SDG 3 すべての人に健康と福祉を

All Science Journal Classification (ASJC) codes

  • 腫瘍学
  • 癌研究

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