骨髓增生异常综合征患者外周血中调节性T细胞和FOXP3亚型表达谱

Q3 Medicine
Advances in Hematology Pub Date : 2018-10-10 eCollection Date: 2018-01-01 DOI:10.1155/2018/8487403
Galina A Dudina, Almira D Donetskova, Marina M Litvina, Alexander N Mitin, Tatiana A Mitina, Sergey A Polyakov
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引用次数: 3

摘要

我们研究了骨髓增生异常综合征患者外周血中调节性T细胞的频率和FOXP3亚型的表达水平,发现调节性T细胞在疾病的所有阶段都显著减少。同时,在未经治疗的患者中,我们观察到FOXP3亚型表达谱向全长分子的转移可能是由于炎症。基于已知的缺乏外显子2的FOXP3分子可能具有更高的功能活性的信息,我们也假设我们的发现可以解释这种疾病中自身免疫性疾病的高风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Regulatory T Cells and Profile of FOXP3 Isoforms Expression in Peripheral Blood of Patients with Myelodysplastic Syndromes.

Regulatory T Cells and Profile of FOXP3 Isoforms Expression in Peripheral Blood of Patients with Myelodysplastic Syndromes.

Regulatory T Cells and Profile of FOXP3 Isoforms Expression in Peripheral Blood of Patients with Myelodysplastic Syndromes.

Regulatory T Cells and Profile of FOXP3 Isoforms Expression in Peripheral Blood of Patients with Myelodysplastic Syndromes.

We have investigated the frequencies of regulatory T cells and the level of FOXP3 isoforms expression in peripheral blood of patients with myelodysplastic syndromes and found the significant reduction of regulatory T cells at all stages of the disease. At the same time in untreated patients, we observed the shift in the FOXP3 isoforms expression profile towards the full-length molecule possibly due to inflammation. Based on the already known information about the potentially higher functional activity of FOXP3 molecule lacking exon 2, we have also hypothesized that our finding may explain the high risk of autoimmune disorders in this disease.

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来源期刊
Advances in Hematology
Advances in Hematology Medicine-Hematology
CiteScore
3.30
自引率
0.00%
发文量
10
审稿时长
15 weeks
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