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Graves病^(131)I或抗甲状腺药物治疗前后外周血CD4^+CD25^+CD127^(low)调节性T细胞的变化 被引量:17

Change of CD4^+ CD25^+ CD127^(low)regulatory T cells in peripheral blood of patients with Graves disease treated by ^(131)I or antithyroid drugs therapy
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摘要 目的探讨调节性T细胞(Treg)在Graves病(GD)患者外周血中变化,以及^(131)I或抗甲状腺药物(ATD)治疗后其变化趋势,寻找评价^(131)I和ATD治疗疗效的新指标。方法健康者40例设为对照组,初诊GD患者40例设为GD组,并将GD组随机分成^(131)I治疗组(20例)及ATD治疗组(20例)。检测^(131)I治疗组、ATD治疗组治疗前、治疗后及对照组CD4^+CD25^+CD127^(low)Treg比例、白介素-10(IL-10)、转化生长因子-β1(TGF-β1)水平,通过统计学软件处理相关结果。结果①治疗前GD组Treg比例较对照组明显降低,差异有统计学意义(P<0.01);②^(131)I治疗组、ATD治疗组治疗后第3个月及第6个月Treg比例较治疗前均升高,差异均有统计学意义(P<0.01);③治疗后第3个月及第6个月,ATD治疗组Treg比例与^(131)I治疗组差异无统计学意义;④治疗前GD组IL-10、TGF-β1水平较对照组均降低,治疗后6个月,细胞因子水平较治疗前均升高,差异均有统计学意义(P<0.05),各时间点^(131)I治疗组与ATD治疗组之间,细胞因子差异无统计学意义。结论 GD患者Treg比例和功能显著降低,治疗后部分恢复,因此,对于甲亢患者,Treg可能是评价免疫状态及治疗后病情缓解的指标之一。 Objective To investigate the changes of regulatory T cells (Treg) in Graves disease (GD) before and after being treated by 131I or antithyroid drugs (ATD), and to seek for new clinical indicators to evaluate the treat- ment response. Methods The study groups included 40 patients with GD ( GD group), 20 of whom were treated by 131i , others were treated by ATD. Forty healthy donors without history of thyroid or autoimmune disease were en- rolled in control group. The proportions of CD4 + CD25 + CD127l^w Treg , IL-10 and TGF-~I were tested before and after treatment respectively. Results The significant decrease in the proportion of CD4 + CD25 + CD1271low WTreg cells in untreated GD patients (GD group) was found compared with the control group; After treatment of 131I or ATD, the proportion of Treg was significantly higher than GD group in 3rd and 6th month ( P 〈 0. 05 ) ; There was no significant difference in the proportion of Treg between ATD group and 1311 group in 3rd and 6th month; (~) The characteristic of cytokine levels( such as IL-10 ,TGF-[31 ) was decreased in untreated GD group, and increased after being treated in 6th month (P 〈 0. 05, respectively). There was no significant difference in the cytokine levels between the 131I group and ATD group at any moment . Conclusion The proportion and function of Treg decrease in GD, but increase in both 131I and ATD therapy patients. The study shows that Treg may play a critical role in af- fecting immunologic function and prognosis of GD patients.
出处 《安徽医科大学学报》 CAS 北大核心 2016年第5期691-695,共5页 Acta Universitatis Medicinalis Anhui
关键词 GRAVES病 调节性T细胞 碘131 抗甲状腺药物 Graves disease regulatory T cells 1311 therapy antithyroid drugs
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参考文献15

  • 1Sakaguchi S, Sakaguchi N, Asano M, et al. Immunologic selftol- erance maintained by activated T cells expressing IL-2 receptor al- phachains (CD25). Breakdown of a single mechanism of self-tol- erance causes various autoimmune diseases [ J ]. Immunol, 1995, 155(3) :1151 -64.
  • 2Saiton O, Nagayama Y. Regulation of Graves' hyperhyroidism with naturally occurring CD4 + CD25 + regulatory T cell in a mouse mod-eli J ]. Endocrinology,2006,147 (5) :2417 - 22.
  • 3Campbell D J, Koch M A. Phenotypical and functional specializa- tion of FOXP3 + regulatory T cell[ J ]. Nat Rev Immunol, 2011,11 (2) :119 -30.
  • 4Liu W, Putnam A L, Xu Y Z, et al. CD127 expression inversely correlates with FoxP3 and suppressive function human CIM + Treg cells[J]. J Exp Meal,2006,203(7) :1701 - 11.
  • 5Hu Y, Tian W, Zhang L L, et al. Function of regulatory T-cells improved by dexamethasone in Graves' disease [ J ]. Eur J Endo- crinol,2012,166(4) :641 -6.
  • 6Mao C M, Wang S, Xiao Y C, et al. Impairment of regulatory ca- pacity of CIM + CD25 + regulatory T ceils mediated by dendritic cell polarization and hyperthyroidism in Graves' disease [ J ]. J Immunol,2011, 186(8): 4734-43.
  • 7李晓玲,王存丰,翟亚萍,汪艳芳,袁慧娟,马跃华,赵志刚.桥本甲状腺炎和格雷夫斯病甲状腺组织中淋巴细胞亚群分布及临床意义[J].中华实用诊断与治疗杂志,2013,27(12):1156-1158. 被引量:12
  • 8Nakano A, Watanabe M, Iida T, et al. Apoptosis-induced decrease of intrathyroidal CIM ( + )CD25 ( + ) regulatory T cells in autoim- mune thyroid diseases [ J ]. Thyroid,2007,17 ( 1 ) :25 - 31.
  • 9Wang H, Zhao S, Tang X, et al. Changes of regulatory T cells in Graves' disease [ J ]. J Huazhong Univ Sci Technolog Med Sci, 2006,26(5): 545 -7.
  • 10钱伟,张强,吴汉妮.Foxp3在Graves病患者外周血单个核细胞中的表达及临床意义[J].中国免疫学杂志,2011,27(1):76-78. 被引量:8

二级参考文献50

  • 1刘世娟,王洪刚,冯永堂,冯志徐.^(131)I治疗Graves病免疫状态变化的规律及临床价值[J].潍坊医学院学报,2005,27(6):410-413. 被引量:4
  • 2Wang S H,Baker J R.The role of apoptosis in thyroid autoimmunity[J].Thyroid,2007;17:975-979.
  • 3Morgan M E,van Bilsen J H,Bakker A M et al.Expression of FOXP3 mRNA is not confined to CD4^+CD25^+ T regulatory cells in humans[J].Hum Immunl,2005;66(1):13-20.
  • 4Hori S,Sakaguchi S.FOXP3:a critical regulator of the development and function of regulatory T cells[J].Microbes Infect,2004;6(8):745-751.
  • 5Shevach E M.CD4^+CD25^+ suppressor T cells:more questions than answers[J].Nat Rev Immunol,2002;2(6):389-400.
  • 6Walker M R,Kasprowicz D J,Gersuk V H et al.Induction of FOXP3 and acquisition of T regulatory activity by stimulated human CD4^+CD25 T cells[J].J Clin Invest,2003;112(9):1437-1443.
  • 7Kasprowiez D J,Smallwood P S,Tyznik A J et al.Scurfin(FOXP3) controls T-dependent immune responses in vivo through regulation of CD4^+ T cell effector function[J].J Immunol,2003;17(3):1216-1223.
  • 8Saitoh O,Nagayama Y.Regulation of Graves hyperthyroidism with naturally occurring CD4^+CD25^+ regulatory T cells in a mouse model[J].Endocrinology,2006;147(5):2417-2422.
  • 9Morris G P,Brown N K,Kong Y C.Naturally-existing CD4^+CD25^+ Foxp3+ regulatory T cells are required for tolerance to experimental autoimmune thyroiditis induced by either exogenous or endogenous autoantigen[J].J Autoimmun,2009;33(1):68-76.
  • 10Rapic M,Stein-Streilein J,Zakarija M et al.Suppression of peripheral blood natural killer cell activity by excess thyroid hormone[J].J Clin Invest,1987;79(2):404-408.

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