miR-142在儿童自身免疫性甲状腺疾病中表达及与Th17/Treg失衡关系的研究

罗平, 辛艳梅, 郭渠莲, 沈兴

中国当代儿科杂志 ›› 2024, Vol. 26 ›› Issue (6) : 605-610.

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中国当代儿科杂志 ›› 2024, Vol. 26 ›› Issue (6) : 605-610. DOI: 10.7499/j.issn.1008-8830.2312017
论著·临床研究

miR-142在儿童自身免疫性甲状腺疾病中表达及与Th17/Treg失衡关系的研究

  • 罗平, 辛艳梅, 郭渠莲, 沈兴
作者信息 +

Expression of miR-142 and its relationship with Th17/Treg imbalance in children with autoimmune thyroid disease

  • LUO Ping, XIN Yan-Mei, GUO Qu-Lian, SHEN Xing
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文章历史 +

摘要

目的 探究微小RNA-142(microRNA-142, miR-142)在儿童自身免疫性甲状腺疾病(autoimmune thyroid disease, AITD)中表达及其与辅助性T细胞17(helper T cell 17, Th17)/调节性T细胞(regulatory T cell, Treg)失衡的关系。 方法 前瞻性选取2019年1月—2022年12月住院治疗的89例AITD患儿为研究对象,包括48例Graves病患儿(Graves disease, GD;设为GD组)和41例桥本甲状腺炎患儿(Hashimoto thyroiditis, HT;设为HT组),另选取55例同期体检的健康儿童为对照组,比较各组血清miR-142、甲状腺球蛋白抗体(antithyroglobulin antibody, TGAb)、抗甲状腺过氧化物酶抗体(antithyroperoxidase antibody, TPOAb)、Th17/Treg及白细胞介素-17(interleukin-17, IL-17)表达差异。 结果 GD组和HT组miR-142、TPOAb、TGAb、Th17、Th17/Treg、IL-17表达高于对照组,Treg水平低于对照组(P<0.05)。Pearson相关分析显示,GD组miR-142与TPOAb、TGAb、Th17、Th17/Treg、IL-17呈正相关(分别r=0.711、0.728、0.785、0.716、0.709,P<0.001),与Treg呈负相关(r=-0.725,P<0.001);HT组miR-142与TPOAb、TGAb呈正相关(分别r=0.752、0.717,P<0.001)。 结论 miR-142在儿童AITD中高表达,且其表达可能与GD患儿Th17/Treg失衡有关。

Abstract

Objective To investigate the expression of microRNA-142 (miR-142) in children with autoimmune thyroid disease (AITD) and its relationship with the imbalance of helper T cell 17 (Th17) and regulatory T cell (Treg). Methods A total of 89 children hospitalized for AITD from January 2019 to December 2022 were prospectively selected as the study subjects, including 48 children with Graves' disease (GD group) and 41 children with Hashimoto's thyroiditis (HT group). Additionally, 55 healthy children undergoing physical examinations during the same period were selected as the control group. The differences in serum miR-142, antithyroglobulin antibody (TGAb), antithyroperoxidase antibody (TPOAb), Th17/Treg, and interleukin-17 (IL-17) expression were compared among the groups. Results The expression of miR-142, TPOAb, TGAb, Th17, Th17/Treg, and IL-17 in the GD group and HT group was higher than that in the control group, while Treg was lower than that in the control group (P<0.05). Pearson correlation analysis revealed that in the GD group, miR-142 was positively correlated with TPOAb, TGAb, Th17, Th17/Treg, and IL-17 (r=0.711, 0.728, 0.785, 0.716, 0.709, respectively; P<0.001) and negatively correlated with Treg (r=-0.725, P<0.001); in the HT group, miR-142 was positively correlated with TPOAb and TGAb (r=0.752, 0.717, respectively; P<0.001). Conclusions miR-142 is highly expressed in children with AITD, and its expression may be related to the Th17/Treg imbalance in children with GD.

关键词

自身免疫性甲状腺疾病 / miR-142 / 免疫平衡 / 辅助性T细胞17 / 调节性T细胞 / 儿童

Key words

Autoimmune thyroid disease / miR-142 / Immune balance / Helper T cell 17 / Regulatory T cell / Child

引用本文

导出引用
罗平, 辛艳梅, 郭渠莲, 沈兴. miR-142在儿童自身免疫性甲状腺疾病中表达及与Th17/Treg失衡关系的研究[J]. 中国当代儿科杂志. 2024, 26(6): 605-610 https://doi.org/10.7499/j.issn.1008-8830.2312017
LUO Ping, XIN Yan-Mei, GUO Qu-Lian, SHEN Xing. Expression of miR-142 and its relationship with Th17/Treg imbalance in children with autoimmune thyroid disease[J]. Chinese Journal of Contemporary Pediatrics. 2024, 26(6): 605-610 https://doi.org/10.7499/j.issn.1008-8830.2312017

参考文献

1 夏秦, 陈临琪, 陈婷. 儿童自身免疫性甲状腺疾病发病机制的研究进展[J]. 医学综述, 2021, 27(3): 428-435. DOI: 10.3969/j.issn.1006-2084.2021.03.003.
2 Wang Y, Fang S, Zhou H. Pathogenic role of Th17 cells in autoimmune thyroid disease and their underlying mechanisms[J]. Best Pract Res Clin Endocrinol Metab, 2023, 37(2): 101743. PMID: 36841747. DOI: 10.1016/j.beem.2023.101743.
3 李媛, 秦廷玉, 郭龙, 等. miR-142-5p靶向调控叉头转录蛋白O亚族3介导辅助性T细胞17细胞炎性反应促进自身免疫性葡萄膜炎的发展[J]. 中华眼底病杂志, 2021, 37(7): 533-541. DOI: 10.3760/cma.j.cn511434-20201203-00602.
4 Mandolesi G, De Vito F, Musella A, et al. miR-142-3p is a key regulator of IL-1β-dependent synaptopathy in neuroinflammation[J]. J Neurosci, 2017, 37(3): 546-561. PMID: 28100738. PMCID: PMC6596761. DOI: 10.1523/JNEUROSCI.0851-16.2016.
5 中华医学会内分泌学分会《中国甲状腺疾病诊治指南》编写组. 中国甲状腺疾病诊治指南——甲状腺功能亢进症[J]. 中华内科杂志, 2007, 46(10): 876-882. DOI: 10.3760/j.issn:0578-1426.2007.10.035.
6 中华医学会内分泌学分会, 《中国甲状腺疾病诊治指南》编写组. 中国甲状腺疾病诊治指南——甲状腺炎[J]. 中华内科杂志, 2008, 47(9): 784-788. DOI: 10.3321/j.issn:0578-1426.2008.09.032.
7 刘敏杰, 李露, 田红艳. 自身免疫性甲状腺疾病患者血清甲状腺过氧化物酶抗体水平与其代谢紊乱的关系[J]. 临床和实验医学杂志, 2021, 20(23): 2561-2564. DOI: 10.3969/j.issn.1671-4695.2021.23.027.
8 Chen A, Huang L, Zhang L. Helper T cell 17 and regulatory T cell levels in peripheral blood of newly diagnosed patients with autoimmune thyroid disease: a meta-analysis[J]. Horm Metab Res, 2023, 55(1): 40-50. PMID: 36332627. DOI: 10.1055/a-1972-5787.
9 Cao Y, Jin X, Sun Y, et al. Therapeutic effect of mesenchymal stem cell on Hashimoto's thyroiditis in a rat model by modulating Th17/Treg cell balance[J]. Autoimmunity, 2020, 53(1): 35-45. PMID: 31793369. DOI: 10.1080/08916934.2019.1697689.
10 Torimoto K, Okada Y, Nakayamada S, et al. Comprehensive immunophenotypic analysis reveals the pathological involvement of Th17 cells in Graves' disease[J]. Sci Rep, 2022, 12(1): 16880. PMID: 36207336. PMCID: PMC9546934. DOI: 10.1038/s41598-022-19556-z.
11 林凯, 齐育英, 王开银, 等. 免疫性甲状腺疾病患者肠道菌群分布及其对Th17/Treg细胞的影响[J]. 中国微生态学杂志, 2022, 34(3): 318-322. DOI: 10.13381/j.cnki.cjm.202203014.
12 Liu HY, Shi ZY, Fan D, et al. Absolute reduction in peripheral regulatory T cells in patients with Graves' disease and post-treatment recovery[J]. Mol Immunol, 2022, 144: 49-57. PMID: 35189399. DOI: 10.1016/j.molimm.2022.02.004.
13 Cortes-Troncoso J, Jang SI, Perez P, et al. T cell exosome-derived miR-142-3p impairs glandular cell function in Sj?gren's syndrome[J]. JCI insight, 2020, 5(9): 133497. PMID: 32376798. PMCID: PMC7253014. DOI: 10.1172/jci.insight.133497.
14 De Vito F, Balletta S, Caioli S, et al. MiR-142-3p is a critical modulator of TNF-mediated neuronal toxicity in multiple sclerosis[J]. Curr Neuropharmacol, 2023, 21(12): 2567-2582. PMID: 37021418. PMCID: PMC10616916. DOI: 10.2174/1570159X21666230404103914.
15 王征, 张浩, 李伟汉, 等. 自身免疫性甲状腺炎甲状腺组织和外周血单个核细胞中微小RNA-142-3p、微小RNA-150表达及临床意义[J]. 安徽医药, 2021, 25(8): 1642-1646. DOI: 10.3969/j.issn.1009-6469.2021.08.039.
16 Bayomy NR, Abo Alfottoh WM, Ali Eldeep SA, et al. Mir-142-5p as an indicator of autoimmune processes in childhood idiopathic nephrotic syndrome and as a part of microRNAs expression panels for its diagnosis and prediction of response to steroid treatment[J]. Mol Immunol, 2022, 141: 21-32. PMID: 34785326. DOI: 10.1016/j.molimm.2021.11.004.
17 De Vito F, Musella A, Fresegna D, et al. MiR-142-3p regulates synaptopathy-driven disease progression in multiple sclerosis[J]. Neuropathol Appl Neurobiol, 2022, 48(2): e12765. PMID: 34490928. PMCID: PMC9291627. DOI: 10.1111/nan.12765.
18 周伟清, 庄一心, 沈卫星, 等. 甲状腺癌患者血清let-7e、miR-142表达及其与Th17/Treg的相关性分析[J]. 疑难病杂志, 2020, 19(4): 362-366. DOI: 10.3969/j.issn.1671-6450.2020.04.009.
19 Li G, He L, Huang J, et al. miR-142-3p encapsulated in T lymphocyte-derived tissue small extracellular vesicles induces Treg function defect and thyrocyte destruction in Hashimoto's thyroiditis[J]. BMC Med, 2023, 21(1): 206. PMID: 37280674. PMCID: PMC10242775. DOI: 10.1186/s12916-023-02914-7.

基金

四川省科技计划资助(2022YFS0622);泸州市人民政府-西南医科大学科技战略合作项目(2023LZXNYDJ047)。

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