绝经后雌激素不足妇女外周血T辅助17 (Th17)细胞表型的表征

IF 2.1 4区 医学 Q3 HEMATOLOGY
Hetal Bhadricha , Vainav Patel , Anushree Patil , Suchitra Surve , Meena Desai
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引用次数: 1

摘要

在过去的几年里,Th17细胞被认为是骨质疏松症发病机制的关键因素。尽管在小鼠模型中进行了广泛的研究,但骨质疏松妇女Th17细胞的全面特征尚不明确。因此,我们旨在检测健康和骨质疏松妇女的外周Th17细胞频率和表型。我们的结果表明,Th17细胞主要是CD4+CD45RA−CCR7−HALDR+CR6lowT细胞。与前-N相比,后-L显示Th17比例增加,同时Th1细胞减少。与前-N和后-L相比,效应记忆CD4+T细胞中的Th17细胞频率在后-N中显著升高,而效应记忆亚群中的Th1细胞减少。与前N相比,后N和后L均降低了双阳性Th1-Th17细胞的频率,并增加了Th17细胞上HLA-DR的表达。因此,我们的研究表明,在雌激素不足的绝经后妇女中,Th17细胞频率增加,Th1细胞频率降低,具有效应记忆表型,并与衰老过程相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of peripheral T helper 17 (Th17) cells phenotype in postmenopausal women with estrogen insufficiency

Over the past few years, Th17 cells is considered a key player in osteoporosis pathogenesis. Although extensively studied in murine models, comprehensive Th17 cell characterization in osteoporotic women is elusive. We thus aimed to examine peripheral Th17 cells frequency and phenotypes in healthy and osteoporotic women. Our results demonstrated that Th17 cells were primarily CD4+CD45RACCR7HALDR+CCR6lowT-cells. Compared to Pre-N, Post-L showed increased proportion of Th17 with concomitant decrease in Th1 cells. The Th17 cells frequency in effector memory CD4+ T cells was significantly elevated in Post-N with a decrease of Th1 cells in effector memory subsets compared to Pre-N and Post-L. Both Post-N and Post-L had decreased frequency of dual positive Th1-Th17 cells and increased HLA-DR expression on Th17 cells compared to Pre-N. Thus, our study demonstrates increased Th17 cells frequency and reduced Th1 cells frequency with effector memory phenotype in postmenopausal women with estrogen insufficiency and correlates with aging process.

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来源期刊
CiteScore
4.90
自引率
0.00%
发文量
42
审稿时长
14 days
期刊介绍: Blood Cells, Molecules & Diseases emphasizes not only blood cells, but also covers the molecular basis of hematologic disease and studies of the diseases themselves. This is an invaluable resource to all those interested in the study of hematology, cell biology, immunology, and human genetics.
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