同种异体干细胞移植后3个月HLA-DR+CD3+ T细胞减少预示严重的慢性GvHD和移植相关死亡率。

IF 3.1 3区 医学 Q3 CELL BIOLOGY
Stefan Koeck, Gabriele Hetzenauer, Ines Peschel-Schaar, Dominik Wolf, Normann Steiner, David Nachbaur
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引用次数: 0

摘要

慢性移植物抗宿主病(cGvHD)是同种异体干细胞移植(HSCT)后移植相关死亡率(TRM)的主要晚期决定因素。我们研究了外周血活化HLA-DR+CD3+ T细胞作为一种新的生物标志物的预测价值。本次回顾性分析共纳入107例患者。造血干细胞移植后3个月,用流式细胞术检测外周血HLA-DR+CD3+ T细胞。A HLA-DR+CD3+ T细胞计数
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Decreased HLA-DR+CD3+ T cells three months after allogeneic stem cell transplantation predict severe chronic GvHD and transplant-related mortality.

Chronic graft vs host disease (cGvHD) is a major late determinant of transplant related mortality (TRM) after allogeneic hematopoietic stem cell transplantation (HSCT). We investigated the predictive value of peripheral blood activated HLA-DR+CD3+ T cells as a novel biomarker. In total, 107 patients were included in this retrospective analysis. Peripheral blood HLA-DR+CD3+ T cells were measured by flow cytometry 3 mo after HSCT. A HLA-DR+CD3+ T cell count <140 cells/µL at month 3 after HSCT correlated significantly with an increased TRM. A HLA-DR+CD3+ T cell count <100 cells/µL was associated with a higher rate of cGvHD grade 2 to 3. Subgroup analyses revealed significant results for TRM and cGvHD grade 2 to 3 for patients with a reduced intensity conditioning. In summary, low HLA-DR+CD3+ T cells in the peripheral blood 3 mo after HSCT may represent a novel biomarker to identify patients with an increased risk for TRM and cGvHD grade 2 to 3.

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来源期刊
Journal of Leukocyte Biology
Journal of Leukocyte Biology 医学-免疫学
CiteScore
11.50
自引率
0.00%
发文量
358
审稿时长
2 months
期刊介绍: JLB is a peer-reviewed, academic journal published by the Society for Leukocyte Biology for its members and the community of immunobiologists. The journal publishes papers devoted to the exploration of the cellular and molecular biology of granulocytes, mononuclear phagocytes, lymphocytes, NK cells, and other cells involved in host physiology and defense/resistance against disease. Since all cells in the body can directly or indirectly contribute to the maintenance of the integrity of the organism and restoration of homeostasis through repair, JLB also considers articles involving epithelial, endothelial, fibroblastic, neural, and other somatic cell types participating in host defense. Studies covering pathophysiology, cell development, differentiation and trafficking; fundamental, translational and clinical immunology, inflammation, extracellular mediators and effector molecules; receptors, signal transduction and genes are considered relevant. Research articles and reviews that provide a novel understanding in any of these fields are given priority as well as technical advances related to leukocyte research methods.
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