期刊文献+

变应性接触性皮炎模型鼠体内Th17细胞活性变化 被引量:2

Changes of Activity of Th17 Cells in a Mouse Model of Allergic Contact Dermatitis
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摘要 目的:研究变应性接触性皮炎(allergic contact dermatitis,ACD)模型鼠外周血及皮损处Th17细胞活性变化情况及其意义。方法:利用2,4-二硝氟苯(DNFB)诱导构建ACD小鼠模型,分别于激发前及激发后的第3、6、9、12、24 h取小鼠耳组织及外周血,评估小鼠耳组织炎症情况,采用实时荧光定量PCR法检测小鼠皮损处IL-17及RORγt mRNA的表达水平,利用酶联免疫吸附试验检测血清中IL-17水平。结果:激发后24 h内小鼠耳组织肿胀程度逐渐加重,皮损中IL-17和RORγt mRNA表达量也逐渐升高,激发后各组与激发前组比较差异有统计学意义(均P<0.05);耳组织IL-17和RORγt mRNA表达量与其肿胀程度呈正相关;激发后小鼠血清中IL-17水平升高,在6小时达到最高,随后逐渐下降。结论:在ACD小鼠的急性炎症期,皮损及外周血中Th17细胞活性增强,并且局部皮损处的Th17细胞活性与炎症程度密切正相关。 Objective :To study the changes and significance of Thl7 cells activity in a mouse model of allergic contact dermatitis (ACD). Methods:The ACD mouse model was established with 2,4- dinitrofluorobenzene (DNFB). Ear swelling response was observed at six time points: before elicitation, 3h,6h,9h,12h,24h after elicitation. Meanwhile RT-RCR was conducted to detect the mRNA of IL-17 and RORγt in ear tissues. The level of IL-17 in peripheral blood was de- tected by ELISA. Results: The degree of inflammation and the expression of both IL-17 and RORγt mRNA in ear tissues went up gradually after elicitation. They were significantly higher than that before elicitation (P 〈 0. 05 ). The degree of inflammation was positively correlated with the expression of IL-17 and RORγt mRNA in ear tissues. The level of IL-17 in peripheral blood went up to the peak 6h after elicitation and then declined gradually. Conclusion:The results demonstrate the activity of Th17 cells increase in acute inflammation of the ACD mouse model. The degree of inflammation is significantly positively correlated to the activity of Th17 cells in ear tissues.
出处 《皮肤性病诊疗学杂志》 2012年第6期343-347,共5页 Journal of Diagnosis and Therapy on Dermato-venereology
基金 广东省科技计划项目(编号:2009B030801090)
关键词 TH17 变应性接触性皮炎 Th17 cells Allergic contact dermatitis
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参考文献8

  • 1Kolls JK, Linden A. Interleukin-17 family members and inflammation [ J ]. Immunity, 2004, 21 (4) :467-476.
  • 2Ivanov II, Zhou L, Littman DR. Transcriptional regula- tion of Thl7 cell differentiation [ J]. Sere in Immunol, 2007, 9(6) :409-417.
  • 3Scholzen TE, Stander S, Riemann H, et al. Modulation of cutaneous inflammation by angiotensin- converting en- zyme[J]. J Immunol, 2003, 70(7): 3866-3873.
  • 4李圆圆,阎春林,马莉,郑志忠.变应性接触性皮炎小鼠模型评价指标探讨[J].中国实验动物学报,2008,16(5):353-356. 被引量:10
  • 5Ouyang W, Kolls JK, Zheng Y. The biological functions of T helper 17 cell effector cytokines in inflammation[ J]. Immunity, 2008,28 (4) : 454-467.
  • 6Larsen JM, Bonefeld CM, Poulsen SS, et al. IL-23 and Thl7-mediated inflammation in human allergic contact dermatitis[J]. J Allergy Clin Immunol, 2009,123(2), 486-492.
  • 7Nakae S, Komiyama Y, Nambu A, et al. Antigen-specif- ic T cell sensitization is impaired in IL-17-deficient mice, causing suppression of allergic cellular and humoral re- sponses[J]. Immunity, 2002, 17(3) :375-387.
  • 8Mitsui G, Mitsui K, Hirano T, et al. Kinetic profiles of sequential gene expressions for chemokines in mice with contact hypersensitivity [ J ]. Immunol Let, 2003, 86 (2) : 191-197.

二级参考文献8

  • 1Saint-Mezard P, Krasteva M, Chavagnac C, et al. Afferent and efferent phases of allergic contact dermatitis (ACD) can be induced after a single skin contact with haptens: evidence using a mouse model of primary ACD[J]. J Invest Dennatol, 2003, 120(4) :641 - 647.
  • 2Ausaneya U, Kawada A, Aragane Y. ltraconazole suppresses an elicitation phase of a contact hypersensitivity reaction [ J]. J Invest Dermatol, 2006, 126(5) : 1028 - 1035.
  • 3Waltz SE, Eaton L, Toney-Earley K, et al. Ron-mediated cytoplasmic signaling is dispensable for viability but is required to limit inflammatory responses[J]. J Clin Invest, 2001, 108(4):567 - 576.
  • 4Hopkins JE, Naisbitt DJ, Kitteringham NR, et al. Selective haptenation of cellular or extracellular protein by chemical allergens: association with cytokine polarization[ J]. Chem Res Toxicol. 2005, 18(2) :375 - 381.
  • 5Wang B, Fujisawa H, Zhuang L, et al. CD4 + Th1 and CD8 + type 1 cytotoxic T cells both play a crucial role in the full development of contact hypersensitivity [ J ]. J Immunol, 2000, 165 (12) :6783 - 6790.
  • 6Woolhiser MR, Munson AE, Meade BJ. Comparison of mouse strains using the local lymph node assay[J]. Toxicology, 2000, 146 (2 - 3) :221 - 227.
  • 7van den Berg FA, Baken KA, Vermeulen JP, et al. Use of the local lymph node assay in assessment of immune function [ J ]. Toxicology, 2005, 211 ( 1 - 2) : 107 - 114.
  • 8樊粤光,梁笃,刘建仁,李雄,王海彬,何伟,张德兴,范光顺,杨荣建.中药M对兔内皮细胞增殖影响的初步研究[J].中国实验动物学报,2003,11(3):181-183. 被引量:2

共引文献9

同被引文献14

  • 1陈凯.著名中医皮外科专家赵炳南教授临床经验及特色疗法[J].中国中西医结合皮肤性病学杂志,2004,3(3):129-132. 被引量:22
  • 2杨西群,陈德宇,杜宇,廖勇梅.祛风止痒口服液对豚鼠变应性接触性皮炎的影响及其作用机制研究[J].中国中西医结合皮肤性病学杂志,2004,3(3):141-144. 被引量:7
  • 3Vocanson M,Hennino A,Rozieres A,et al.Effector and regulatory mechanisms in allergic contact dermatitis[J].Allergy,2009,64(12):1699-1714.
  • 4Wakkach A,Fournier N,Brun V,et al.Characterization of denritic cells that induce tolerance and T regulatory 1 cell differentiation invivo[J].Immunity,2003,18:605-617.
  • 5Fantini M C,Becker C,Monteleone G,et al.Cutting edge:TGFbeta induces a regulatory phenotype in CD4+CD25-T cells through Foxp3 induction and down-regulation of Smad7[J].J Immunol,2004,172:5149-5153.
  • 6Damsker J M,Hansen A M,Caspi R R.Th1 and Th17 cells[J].Ann N Y Acad Sci,2010,1183(1):211-221.
  • 7Louten J,Boniface K,de Waal Malefyt R.Development and function of TH17 cells in health and disease[J].J Allergy Clin Immunol,2009,123(5):1004-1011.
  • 8Ivanov I I,Zhou L,Littman D R.Transcriptional regulation of Th17 cell differentiation[J].Semin Immunol,2007,19(6):409-417.
  • 9Jietang Mai,Hong Wang,and Xiao-Feng Yang.T Helper 17Cells Interplay with CD4+CD25high Foxp3+Tregs in Regulation of Inflammations and Autoimmune Diseases[J].Front Biosci,2010,15:986-1006.
  • 10Korn T,Bettelli E,Gao W,et al.IL-21 initiates an alternative pathway to induce proinflammatory T(H)17 cell[J].Nature,2007,448(52):484-487.

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