Study on the correlation between Th17/ Treg and IL-17 and pancreatic B cell function in type 1 diabetes mellitus

  • YIN Qingqing ,
  • YANG Lulu ,
  • HU Xiaolei ,
  • SHI Zhaoming ,
  • YANG Qingqing ,
  • SUN Weihua
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  • The First Affiliated Hospital of Bengbu Medical College, Bengbu 233000, China

Received date: 2023-12-08

  Online published: 2025-02-24

Abstract

Objective: To observe the expression levels of regulatory T cells (Treg), helper T cells 17 (Th17) and cytokine interleukin 17 (IL-17) in peripheral blood of patients with type 1 diabetes mellitus (T1DM) and latent autoimmune diabetes in adults (LADA), with the purpose of exploring the role of Th17/Treg in T1DM by analyzing its correlation with islet-reactive B cells function in T1DM. Methods: A total of 78 cases of T1DM patients, LADA patients and normal healthy people who were admitted in the Endocrinology Department, the First Affiliated Hospital of Bengbu Medical College from December 2021 to June 2022 were selected and divided into the T1DM group, LADA group and normal control (NC) group. Serum IL-17 was detected by ELISA method. Proportions of Th17 and Treg cells were detected by flow cytometry, and the differences of Th17 and IL-17 expression among the three groups were compared. Results: The proportion of Treg cells in the T1DM group and LADA group was significantly lower than that in the NC group, and it was significantly lower in the T1DM group than that in the LADA group. The expression levels of Th17 and IL-17 in the T1DM group and LADA group were significantly higher than those in the NC group, but there was no significant difference between the T1DM group and LADA group. The results of Pearson correlation analysis showed that serum IL-17 and Th17 were negatively correlated with FCP and 2h-CP (IL-17: r/P=-0.273, 0.016, -0.352, 0.002), Treg was positively correlated with FCP and 2h-CP (r/P=0.494/<0.001, 0.575/<0.001). Multivariate logistic regression analysis showed that IL-17 was a risk factor to T1DM and LADA by taking T1DM, LADA, NC as dependent variables(1=T1DM,2=LADA,3=NC), Th17 was a risk factor to T1DM, and Treg was a protective factor to T1DM and LADA. Conclusion: T1DM and LADA patients have unbalanced Th 17 / Treg ratio in vivo, manifested by increased expression level of Th 17 and IL-17 and decreased expression level of Treg, it may be associated with functional impairment of islet-reactive B cells, which could lead to the occurrence and development of T1DM.

Cite this article

YIN Qingqing , YANG Lulu , HU Xiaolei , SHI Zhaoming , YANG Qingqing , SUN Weihua . Study on the correlation between Th17/ Treg and IL-17 and pancreatic B cell function in type 1 diabetes mellitus[J]. Journal of Baotou Medical College, 2025 , 41(1) : 91 -96 . DOI: 10.16833/j.cnki.jbmc.2025.01.017

References

[1] Weng JP, Zhou ZG, Guo LX. Incidence of type 1 diabetes in China, 2010-13: population based study[J]. BMJ, 2018, 360: j5295.
[2] Rawshani A, Sattar N, Franzén S, et al. Excess mortality and cardiovascular disease in young adults with type 1 diabetes in relation to age at onset: a nationwide, register-based cohort study[J]. The Lancet, 2018, 392(10146): 477-486.
[3] Raphael I, Nalawade S, Eagar TN, et al. T cell subsets and their signature cytokines in autoimmune and inflammatory diseases[J]. Cytokine, 2015, 74(1): 5-17.
[4] Abdel-Moneim A, Bakery HH, Allam G. The potential pathogenic role of IL-17/Th17 cells in both type 1 and type 2 diabetes mellitus[J]. Biomedicine & Pharmacotherapy, 2018, 101: 287-292.
[5] Li BW, Ren Q, Ling JZ, et al. The change of Th17/Treg cells and IL-10/IL-17 in Chinese children with Henoch-Schonlein purpura: a PRISMA-compliant meta-analysis[J]. Medicine, 2019, 98(3): e13991.
[6] 翁建平. 我国1型糖尿病的流行病学研究与疾病负担[J]. 中国科学: 生命科学, 2018, 48(8): 834-839.
[7] Rouvier E, Luciani MF, Mattéi MG, et al. CTLA-8, cloned from an activated T cell, bearing AU-rich messenger RNA instability sequences, and homologous to a herpesvirus saimiri gene[J]. The Journal of Immunology, 1993, 150(12): 5445-5456.
[8] 刘蔚, 王天刚, 祝虹霞, 等. 柴黄清胰活血颗粒对重症急性胰腺炎患者辅助性T细胞17及其相关因子的调节作用[J]. 中医临床研究, 2020, 12(29): 56-59.
[9] 解松龄, 蒋正, 赵涛, 等. 辅助性T细胞17及其细胞因子在急性胰腺炎患者诊治中的作用[J]. 中华肝胆外科杂志, 2020(2): 134-138.
[10] Zhang X, Yuan YP, Pan ZP, et al. Elevated circulating IL-17 level is associated with inflammatory arthritis and disease activity: a meta-analysis[J]. Clinica Chimica Acta, 2019, 496: 76-83.
[11] Satoh Y, Nakano K, Yoshinari H, et al. A case of refractory lupus nephritis complicated by psoriasis vulgaris that was controlled with secukinumab[J]. Lupus, 2018, 27(7): 1202-1206.
[12] Liu YL, Yan WM, Yuan W, et al. Treg/Th17 imbalance is associated with poor autoimmune hepatitis prognosis[J]. Clinical Immunology, 2019, 198: 79-88.
[13] 孙卫华, 薛丽, 殷晴晴, 等. 1型糖尿病患者IL-17与TNF-α的表达及临床意义[J]. 河北北方学院学报(自然科学版), 2021, 37(6): 6-10.
[14] 赵成玉, 黄香丽, 李占全, 等. 1型糖尿病患者Th17细胞比例及其相关细胞因子表达水平的变化[J]. 中国全科医学, 2017, 20(9): 1061-1066.
[15] Emamaullee JA, Davis J, Merani S, et al. Inhibition of Th17 cells regulates autoimmune diabetes in NOD mice[J]. Diabetes, 2009, 58(6): 1302-1311.
[16] 郭红, 米克拉依·加帕尔, 余亮, 等. 1型糖尿病患儿血清程序性细胞死亡受体1及其配体和相关细胞因子水平变化及临床意义[J]. 中国医药, 2021, 16(9): 1342-1345.
[17] 王丽丽, 何振生. 补肾活血泄浊汤对2型糖尿病肾病肾功能衰竭患者肾功能及血清炎症因子的影响[J]. 中国中医急症, 2019, 28(6): 996-998.
[18] Feng XL, Jiang S, Leung WT, et al. BuShen HuoXue decoction promotes decidual stromal cell proliferation via the PI3K/AKT pathway in unexplained recurrent spontaneous abortion[J]. Evidence-Based Complementary and Alternative Medicine, 2020, 2020: 1-11.
[19] Abdel-Moneim A, Bakery HH, Allam G. The potential pathogenic role of IL-17/Th17 cells in both type 1 and type 2 diabetes mellitus[J]. Biomedicine & Pharmacotherapy, 2018, 101: 287-292.
[20] 王智峰, 李秋梅, 姜啸, 等. Foxp3+Treg、Tim-3和CTLA-4水平与T1DM患者病情发生发展的关系[J]. 国际检验医学杂志, 2020, 41(24): 3028-3030, 3036.
[21] Luczyński W, Wawrusiewicz-Kurylonek N, Iłendo E, et al. Generation of functional t-regulatory cells in children with metabolic syndrome[J]. Arch Immunol Ther Exp (Warsz), 2012, 60(6): 487-495.
[22] Ryba-Stanisławowska M, Skrzypkowska M, Myšliwiec M, et al. Loss of the balance between CD4+Foxp3+regulatory T cells and CD4+IL17A+Th17 cells in patients with type 1 diabetes[J]. Human Immunology, 2013, 74(6): 701-707.
[23] Bending D, Ono M. From stability to dynamics: understanding molecular mechanisms of regulatory T cells through Foxp3 transcriptional dynamics[J]. Clinical & Experimental Immunology, 2019, 197(1): 14-23.
[24] Polonsky WH, Arsenault J, Fisher L, et al. Initiating insulin: how to help people with type 2 diabetes start and continue insulin successfully[J]. International Journal of Clinical Practice, 2018, 71(8): e12973.
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