Volume 19 Issue 4
Apr.  2021
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HE Cheng-cheng, JIN Guo-xi, BI Ya-xin. Expression of B cell activating factor and interleukin-21 in the plasma of patients with Hashimoto's thyroiditis[J]. Chinese Journal of General Practice, 2021, 19(4): 568-571. doi: 10.16766/j.cnki.issn.1674-4152.001863
Citation: HE Cheng-cheng, JIN Guo-xi, BI Ya-xin. Expression of B cell activating factor and interleukin-21 in the plasma of patients with Hashimoto's thyroiditis[J]. Chinese Journal of General Practice, 2021, 19(4): 568-571. doi: 10.16766/j.cnki.issn.1674-4152.001863

Expression of B cell activating factor and interleukin-21 in the plasma of patients with Hashimoto's thyroiditis

doi: 10.16766/j.cnki.issn.1674-4152.001863
Funds:

 KJ2019ZD29

  • Received Date: 2020-08-31
    Available Online: 2022-02-16
  •   Objective  To investigate the expression of human B cell activating factor (BAFF) and interleukin-21 (IL-21) in the plasma of patients with Hashimoto's thyroiditis (HT) and explore their roles in the pathogenesis of HT.  Methods  Patients with HT in the Endocrinology Clinic of The First Affiliated Hospital of Bengbu Medical College from December 2019 to June 2020 were selected as the observation group (HT group, n= 82). According to thyroid functions, the HT group was further divided into an NHT group (normal thyroid function, n= 39) and an SHT group (hypothyroidism or subclinical hypothyroidism, n=43). A total of 51 patients (NC group) who visited the hospital for consultation during the same period were designated as the control group. Peripheral venous blood plasma was collected. BAFF and IL-21 were tested via enzyme-linked immunosorbent assay(ELISA). Thyroid function, thyroid microsomal antibody (TMAB) and thyroglobulin antibody (TGAB) were detected via chemiluminescence immunoassay. Data were analysed using SPSS 24.0.  Results  The levels of BAFF and IL-21 in the plasma of the HT group were significantly higher than those of the NC group (all P < 0.05). The levels of BAFF in the SHT group was significantly higher than that in the NHT group (P < 0.05). The plasma levels of BAFF in the patients with HT were positively correlated with TGAB and TMAB (r=0.444 and 0.401, respectively; all P < 0.05). Similarly, IL-21 was positively correlated with TGAB and TMAB (r=0.451 and 0.451, respectively; all P < 0.05). A positive correlation was observed between BAFF and IL-21 (r=0.324, P < 0.05). By contrast, a negative correlation was found between BAFF and total T4(TT4, r=-0.214, P < 0.05). The combined diagnosis of HT with BAFF and IL-21 (AUC=0.896) was more valuable than that of BAFF (AUC=0.862) and IL-21 (AUC=0.809) alone.  Conclusion  BAFF combined with IL-21 has a certain value in the diagnosis of HT. BAFF and IL-21 play an important role in the occurrence and development of HT. Moreover, they participate in the maturation, proliferation and differentiation of B cells. Finally, they participate jointly in the production of TGAB and TMAR.

     

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  • [1]
    方露, 朱武飞, 廖翔宇, 等. 桥本氏甲状腺炎患者年龄、性别分布及自身免疫抗体水平分析[J]. 微循环学杂志, 2020, 30(1): 69-72. doi: 10.3969/j.issn.1005-1740.2020.01.015
    [2]
    王薇, 卢桂芝, 高燕明, 等. 甲状腺针吸细胞学检查的不同年龄段患者临床特点分析[J]. 中华全科医学, 2019, 17(5): 738-741. https://www.cnki.com.cn/Article/CJFDTOTAL-SYQY201905010.htm
    [3]
    LUTY J, RUCKEMANN-DZIURDZINSKA K, WITKOWSKI J M, et al. Immunological aspects of autoimmune thyroid disease-Complex interplay between cells and cytokines[J]. Cytokine, 2019, 116: 128-133. doi: 10.1016/j.cyto.2019.01.003
    [4]
    詹玲, 陈创, 孙圣荣. 免疫微环境在桥本甲状腺炎与甲状腺癌中作用研究进展[J]. 中华实用诊断与治疗杂志, 2020, 34(6): 640-642. https://www.cnki.com.cn/Article/CJFDTOTAL-HNZD202006027.htm
    [5]
    ROBINSON M J, PITT C, BRODIE E J, et al. BAFF, IL-4 and IL-21 separably program germinal center-like phenotype acquisition, BCL6 expression, proliferation and survival of CD40L-activated B cells in vitro[J]. Immunol Cell Biol, 2019, 97(9): 826-839. doi: 10.1111/imcb.12283
    [6]
    ZHAO R Q, ZHANG H H, ZHANG Y, et al. In vivo screen identifies Zdhhc2 as a critical regulator of germinal center B cell differentiation[J]. Front Immunol, 2020, 11: 1025. doi: 10.3389/fimmu.2020.01025
    [7]
    NAKAYAMA Y, KOSEK J, CAPONE L, et al. Aiolos overexpression in systemic lupus erythematosus B Cell subtypes and BAFF-induced memory B cell differentiation are reduced by CC-220 modulation of cereblon activity[J]. J Immunol, 2017, 199(7): 2388-2407. doi: 10.4049/jimmunol.1601725
    [8]
    GHARIBI T, HOSSEINI A, MAROFI F, et al. IL-21 and IL-21-producing T cells are involved in multiple sclerosis severity and progression[J]. Immunol Lett, 2019, 216: 12-20. doi: 10.1016/j.imlet.2019.09.003
    [9]
    DINESH P, RASOOL M. Multifaceted role of IL-21 in rheumatoid arthritis: Current understanding and future perspectives[J]. J Cell Physiol, 2018, 233(5): 3918-3928. doi: 10.1002/jcp.26158
    [10]
    ZHOU H, HU B, ZHAOPENG Z, et al. Elevated circulating T cell subsets and cytokines expression in patients with rheumatoid arthritis[J]. Clin Rheumatol, 2019, 38(7): 1831-1839. doi: 10.1007/s10067-019-04465-w
    [11]
    GENSOUS N, SCHMITT N, RICHEZ C, et al. T follicular helper cells, interleukin-21 and systemic lupus erythematosus[J]. Rheumatology(Oxford), 2017, 56(4): 516-523.
    [12]
    CHENG C W, TANG K T, FANG W F, et al. Synchronized expressions of serum osteopontin and B cell-activating factor in autoimmune thyroid disease[J]. Eur J Clin Invest, 2019, 49(7): e13122. http://www.ncbi.nlm.nih.gov/pubmed/31034586
    [13]
    CHENG C W, WU C Z, TANG K T, et al. Simultaneous measurement of twenty-nine circulating cytokines and growth factors in female patients with overt autoimmune thyroid diseases[J]. Autoimmunity, 2020, 53(5): 261-269. doi: 10.1080/08916934.2020.1755965
    [14]
    FENG Y, QIU T, CHEN H, et al. Association of serum IL-21 and vitamin D concentrations in Chinese children with autoimmune thyroid disease[J]. Clin Chim Acta, 2020, 507: 194-198. doi: 10.1016/j.cca.2020.04.030
    [15]
    RAMOS-LEVI A M, MARAZUELA M. Pathogenesis of thyroid autoimmune disease: the role of cellular mechanisms[J]. Endocrinol Nutr, 2016, 63(8): 421-429. doi: 10.1016/j.endonu.2016.04.003
    [16]
    RYDZEWSKA M, JAROMIN M, PASIEROWSKA I E, et al. Role of the T and B lymphocytes in pathogenesis of autoimmune thyroid diseases[J]. Thyroid Res, 2018, 11: 2. doi: 10.1186/s13044-018-0046-9
    [17]
    MAO J N, SHEN Y S, LUO X Y, et al. Expression of IL-21 in rats with inflammatory bowel disease[J]. Genet Mol Res, 2015, 14(4): 17322-17328. doi: 10.4238/2015.December.16.33
    [18]
    CARRILLO-BALLESTEROS F J, PALAFOX-SANCHEZ C A, FRANCO-TOPETE R A, et al. Expression of BAFF and BAFF receptors in primary Sjogren's syndrome patients with ectopic germinal center-like structures[J]. Clin Exp Med, 2020, 20(4): 615-626. doi: 10.1007/s10238-020-00637-0
    [19]
    VINCENT F B, KANDANE-RATHNAYAKE R, KOELMEYER R, et al. Associations of serum soluble Fas and Fas ligand (FasL) with outcomes in systemic lupus erythematosus[J]. Lupus Sci Med, 2020, 7(1): e000375. doi: 10.1136/lupus-2019-000375
    [20]
    CAMPI I, TOSI D, ROSSI S, et al. B Cell Activating Factor (BAFF) and BAFF receptor expression in autoimmune and nonautoimmune thyroid diseases[J]. Thyroid, 2015, 25(9): 1043-1049. doi: 10.1089/thy.2015.0029
    [21]
    CHENG C W, WU C Z, TANG K T, et al. Simultaneous measurement of twenty-nine circulating cytokines and growth factors in female patients with overt autoimmune thyroid diseases[J]. Autoimmunity, 2020, 53(5): 261-269. doi: 10.1080/08916934.2020.1755965
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