再生障碍性贫血
医学
骨髓增生异常综合症
免疫学
内科学
淋巴细胞亚群
淋巴细胞
贫血
T细胞
免疫系统
骨髓
作者
Hai-Fang Zhang,Zhendong Huang,Xuerun Wu,Qian Li,Zhifeng Yu
出处
期刊:Life Sciences
[Elsevier]
日期:2017-09-20
卷期号:189: 71-75
被引量:9
标识
DOI:10.1016/j.lfs.2017.09.020
摘要
Abstract Aims This study aims to compare the proportion of peripheral blood T lymphocyte subsets and related blood cell and bone marrow cytology indexes between patients with aplastic anemia (AA) and hypoplastic myelodysplastic syndrome (hypo-MDS), and investigate the clinical identification significance. Materials and methods A total of 41 patients with AA and 46 patients with hypo-MDS were collected, and the proportions of peripheral blood T lymphocyte subsets, CD3− CD16/CD56+ NK cells, CD3+ CD57+ T-LGL cells and CD19+ B lymphocytes were detected by flow cytometry. Key findings The CD4+/CD8+ ratio decreased in the AA and hypo-MDS groups, and the difference was statistically significant when compared with that in the control group (P 0.05). The proportions of CD3− CD16/CD56+ NK cells and CD3+ CD57+ T-LGL cells in the hypo-MDS group were distinctly higher than those in the AA group (P Significance Changes of T lymphocyte subsets and the proportions of large granular lymphocytes and B lymphocytes can be utilized as indexes in the differential diagnosis between AA and hypo-MDS.
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