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分析复发性缓解型多发性硬化症患者外周血 CD4+T 淋巴细胞中 mir-34a、mir-199a、mir-30c 和 mir-19a 的表达。

Analysis of the expression of mir-34a, mir-199a, mir-30c and mir-19a in peripheral blood CD4+T lymphocytes of relapsing-remitting multiple sclerosis patients.

机构信息

Immunology Department, School of Medicine, Shahrekord University of Medical Sciences, Shahrekord, Iran; Department of Cellular Biotechnology at Cell Science research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.

Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Non-affiliation communicable disease, Isfahan University of Medical Sciences, Isfahan, Iran; Department of Biology, Nour-e Danesh Institute of Higher Education, Meimeh, Iran; Department of Cellular Biotechnology at Cell Science research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.

出版信息

Gene. 2018 Jun 15;659:109-117. doi: 10.1016/j.gene.2018.03.035. Epub 2018 Mar 15.

Abstract

BACKGROUND

Multiple sclerosis is an immune-mediated inflammatory disease of central nervous system. MicroRNAs play important roles in autoimmune diseases such as MS.

OBJECTIVES

The aim was to evaluate the expression pattern of miR-34a, miR-199a, miR-30c and miR-19a in peripheral blood derived CD4+ T lymphocytes of both relapsing and remitting phases of MS.

METHODS

Blood samples from 40 RRMS patients (20 in relapsing and 20 in remitting phase) and 20 healthy volunteers were taken. CD4+ T cells were isolated. The expression level of miR-34a, miR-199a, miR-30c and miR-19a, and the percentage of Th17 and Treg cells were measured. Expression of master transcription factors of Th17 and Treg cells and several targets of these miRNAs were also evaluated.

RESULTS

Data indicated an increased expression of miR-34a, miR-30c and miR-19a in relapsing phase and decreased expression of miR-199a in remitting phase. ROC curve data add other prestigious information of miR-34a, miR-199a, miR-30c and miR-19a by defining relapsing and remitting phase and also healthy cases with high specificity and sensitivity at a proposed optimum cut-off point.

CONCLUSION

Collectively, we showed a correlation between the four miRNAs with different phases of MS and their possible involvement in differentiation pathways of Th17 cells, as the most important players in MS.

摘要

背景

多发性硬化症是一种中枢神经系统的免疫介导的炎症性疾病。MicroRNAs 在自身免疫性疾病如多发性硬化症中发挥重要作用。

目的

旨在评估 miR-34a、miR-199a、miR-30c 和 miR-19a 在多发性硬化症缓解和复发期外周血 CD4+T 淋巴细胞中的表达模式。

方法

采集 40 例 RRMS 患者(缓解期 20 例,复发期 20 例)和 20 例健康志愿者的血样。分离 CD4+T 细胞。检测 miR-34a、miR-199a、miR-30c 和 miR-19a 的表达水平,Th17 和 Treg 细胞的比例。还评估了 Th17 和 Treg 细胞的主要转录因子和这些 miRNA 的几个靶基因的表达。

结果

数据表明,miR-34a、miR-30c 和 miR-19a 在复发期表达增加,miR-199a 在缓解期表达减少。ROC 曲线数据通过定义复发期和缓解期以及健康病例,以高特异性和敏感性在建议的最佳截断点处为 miR-34a、miR-199a、miR-30c 和 miR-19a 提供了其他有价值的信息。

结论

综上所述,我们显示了四种 miRNAs 与多发性硬化症不同阶段之间的相关性,以及它们在 Th17 细胞分化途径中的可能参与,作为多发性硬化症的最重要参与者。

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