重型再生障碍性贫血患者的 HLA-A*0206 缺陷克隆造血再生,无需明确的免疫抑制治疗。

IF 3.8 2区 医学 Q1 HEMATOLOGY
Yoshitaka Zaimoku, Kazuya Sakai, Noriaki Tsuji, Kazuyoshi Hosomichi, Shinya Yamada, Dung Cao Tran, Miku Kobayashi, Ayana Sugiyama, Kouyuki Hirayasu, Hiroki Mizumaki, Ken Ishiyama, Rikinari Hanayama, Yoshiaki Tomiyama, Shinji Nakao
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引用次数: 0

摘要

我们描述了一名 74 岁重型再生障碍性贫血患者的病例,他的病情持续缓解是由于 HLA 等位基因缺陷克隆的增殖。尽管在使用艾曲波帕和环孢素治疗的初期,全血细胞减少的情况有所恶化,但三系造血功能逐渐恢复,血细胞计数在三年内恢复正常。流式细胞术和深核苷酸测序显示,造血主要由几个具有体细胞突变的克隆支持,这些克隆通过 HLA-A*0206 使抗原递呈失活。这表明,对于拥有 HLA 等位基因缺陷克隆且不能耐受标准疗法的免疫性再生障碍性贫血患者来说,监测免疫逃逸克隆的造血再生可能是一种替代方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Haematopoietic regeneration by HLA-A*0206-deficient clones in severe aplastic anaemia without definitive immunosuppressive treatment

We describe the case of a 74-year-old man with severe aplastic anaemia who experienced persistent remission attributed to proliferation of HLA allele-deficient clones. Despite an initial worsening of pancytopenia with eltrombopag and ciclosporin treatment, gradual trilineage haematopoietic recovery occurred, with blood counts normalizing over 3 years. Flow cytometry and deep nucleotide sequencing revealed that haematopoiesis was primarily supported by several clones with somatic mutations that inactivated antigen presentation via HLA-A*0206. This suggests that monitoring haematopoietic regeneration by immune escape clones could be an alternative approach for immune aplastic anaemia patients who possess HLA allele-deficient clones and cannot tolerate standard therapy.

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来源期刊
CiteScore
8.60
自引率
4.60%
发文量
565
审稿时长
1 months
期刊介绍: The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.
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