养血消风饮对变应性接触性皮炎的作用及免疫学机制研究
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摘要
目的:利用小鼠急、慢性变应性接触性皮炎(ACD)模型,通过动物的病理改变、组织形态学改变评价养血消风饮对急、慢性ACD的药理作用;并通过对相关细胞因及其mRNA、细胞凋亡等的检测,从细胞水平、分子水平对其免疫学机制进行探索,为临床更好地应用该方防治急、慢性ACD提供客观依据。
     材料与方法
     1.实验材料
     (1)实验动物:继康雄性昆明种小鼠。
     (2)实验用药:均采用灌胃给药的方法。中药治疗组采用养血消风饮水煎剂;西药对照组采用氯雷他定片,用蒸馏水溶解制成混浊液;空白组、模型组用等量蒸馏水灌胃。
     2.研究方法
     (1)造模方法:采用DNCB皮肤涂抹的方法分别制备小鼠急、慢性ACD动物模型。
     (2)通过观察养血消风饮对急、慢性ACD小鼠病变耳肿胀度、耳肿胀抑制百分率及脾指数和胸腺指数的影响,初步评价其对小鼠ACD的抑制。
     (3)通过光镜及透射电镜观察养血消风饮对急性ACD小鼠病变局部组织病理以及超微结构的影响,进一步分析养血消风饮对急性ACD病变组织形态学的影响。
     (4)采用ELISA法测定慢性ACD模型小鼠血清中IFN-γ、IL-4的含量,采用RT-PCR方法检测病变组织局部IFN-γmRNA、IL-4mRNA的表达情况,并进行血清中细胞因子的水平与病变组织中mRNA表达的相关分析,从Th1/Th2细胞因子网络平衡的角度进一步深入探讨养血消风饮抑制ACD的免疫学机制。
     (5)采用免疫组化的方法,检测慢性ACD模型小鼠病变组织中细胞因子TNF-α、NF-κBp50、Fas/FasL含量,通过研究慢性ACD发病过程中皮损部位上述细胞因子表达的变化,探求养血消风饮可能的作用机制和环节。
     (6)采用Annexin V-FITC细胞凋亡检测方法,用流式细胞仪对慢性ACD小鼠脾淋巴细胞早期凋亡百分率进行研究,从细胞水平探索养血消风饮能否通过诱导淋巴细胞凋亡下调免疫应答强度,进而抑制ACD的发生。
     结果
     1.养血消风饮可下调急、慢性ACD模型小鼠病变耳的重量差和肿胀度
     急、慢性ACD模型组小鼠的耳重量差值均明显高于空白组(P<0.01),养血消风饮低、中、高剂量组和氯雷他定组的耳重量差与模型组相比均明显减小(P<0.01或P<0.05),在本实验所采用药量范围内,养血消风饮对急性ACD模型的作用无明显量-效依赖关系,对慢性ACD模型的作用呈一定的量-效依赖关系。
     2.养血消风饮可下调急、慢性ACD模型小鼠的脾指数及胸腺指数
     急、慢性ACD模型组小鼠的脾指数、胸腺指数均明显升高(P<0.01);养血消风饮组和氯雷他定均可显著下调急、慢性ACD模型小鼠的脾指数及胸腺指数(P<0.01);养血消风饮对二者的影响均呈现一定的量-效依赖关系。
     3.养血消风饮可减轻急性ACD模型小鼠病变局部组织病理及超微结构的损伤程度
     ACD模型组小鼠背部皮肤的组织病理切片显示:表皮部分坏死缺失,细胞间、细胞内水肿;真皮乳头水肿,真皮内大量炎细胞浸润;胶原纤维间隙增宽;血管扩张,内皮细胞肿胀。用养血消风饮干预后,其皮肤全层结构基本完整,细胞内和细胞间水肿明显减轻,真皮内炎性细胞浸润明显减少。各层损害均较ACD模型组明显减轻。氯雷他定组真皮内炎性细胞浸润数目较养血消风饮组高,其他改变与养血消风饮组大致相同。
     在皮肤超微结构的研究中,ACD模型组小鼠病变皮肤基底细胞、棘细胞均出现萎缩,表皮角质细胞电子密度略增强,基底细胞间连接消失,胞质内细胞器空泡化,细胞核内异染色质浓缩成团块状并趋向核周边化分布;养血消风饮组小鼠病变皮肤基底细胞与棘细胞结构完整,细胞轻度萎缩,细胞间以桥粒连结,核内染色质基本呈均匀分布,线粒体和粗面内质网结构基本完整,空泡化不明显,细胞损伤较模型组明显减轻。氯雷他定组核内染色质部分呈团块状分布,其他改变与养血消风饮组大致相同。
     4.养血消风饮可上调ACD模型小鼠血清中IL-4的含量及下调IFN-γ的含量,同时可上调耳组织中IL-4mRNA的表达水平,下调IFN-γmRNA的表达水平
     慢性ACD模型小鼠血清中IFN-γ的水平明显升高而IL-4的水平明显降低(P<0.01),病变耳组织中有IFN-γmRNA的高表达而IL-4mRNA的表达减少(P<0.01),模型组小鼠的血清IFN-γ/IL-4比值与耳组织中IFN-γmRNA/IL-4mRNA比值均明显升高(P<0.01);养血消风饮或氯雷他定均可明显下调ACD小鼠血清中IFN-γ水平以及耳组织中IFN-γmRNA的表达水平(P<0.01);养血消风饮还可明显上调血清中IL-4水平(P<0.05)以及耳组织中IL-4mRNA的表达水平(P<0.01),氯雷他定则上调血清中IL-4水平而对病变耳组织中IL-4mRNA的表达水平无影响;养血消风饮或氯雷他定均可显著降低IFN-γ/IL-4以及IFN-γmRNA/IL-4mRNA的比值(P<0.01);养血消风饮对IFN-γmRNA/IL-4mRNA比值的影响优于氯雷他定组,而对IFN-γ/IL-4比值的影响二者无显著差异。
     5.养血消风饮可明显下调慢性ACD小鼠病变皮肤组织中TNF-α、NF-κBp50的表达水平,并明显上调Fas和FasL的表达
     慢性ACD小鼠耳组织TNF-α、NF-κBp50表达均明显增加(P<0.01);养血消风饮可以明显下调组织中TNF-α、NF-κBp50表达(P<0.01);氯雷他定组对组织中TNF-α表达的影响不明显(P>0.05),但可以明显下调NF-κBp50表达(P<0.05);养血消风饮组的作用明显优于氯雷他定组(P<0.05或P<0.01)。
     慢性ACD小鼠耳组织Fas、FasL表达均明显增加(P<0.01);养血消风饮可以明显上调组织中Fas、FasL表达(P<0.01):氯雷他定组对二者的影响均不明显(P>0.05)。
     小鼠耳廓皮肤组织中TNF-α与NF-κBp50、Fas与FasL的表达分别呈正相关(相关系数分别为:0.783,P<0.01:0.747,P<0.01)。
     6.养血消风饮可明显促进慢性ACD小鼠脾淋巴细胞早期凋亡
     模型小鼠脾淋巴细胞早期凋亡的百分率明显增加(P<0.01);养血消风饮或氯雷他定均可明显上调小鼠脾淋巴细胞早期凋亡的百分率,养血消风饮组的作用强于氯雷他定组(P<0.01)。
     小鼠脾淋巴细胞早期凋亡的百分率与小鼠耳组织Fas、FasL的表达分别呈正相关(相关系数分别为:0.783,P<0.01;0.785,P<0.01)。
     结论
     1.养血消风饮对小鼠急、慢性ACD均有抑制作用,能减轻其耳廓的肿胀度,并能够抑制病变过程中免疫器官的肿大反应,下调胸腺指数和脾指数;
     2.养血消风饮能够减轻急性ACD小鼠病变局部组织病理及超微结构损伤的程度;
     3.养血消风饮可抑制慢性ACD小鼠Th1型细胞因子、促进Th2型细胞因子的分泌,从而调节Th1/Th2网络平衡:
     4.养血消风饮可明显下调慢性ACD小鼠病变皮肤组织中TNF-α、NF-κBp50的表达水平,可能在转录水平抑制炎症的发生,抑制免疫反应;
     5.养血消风饮可以明显上调慢性ACD小鼠病变皮肤组织中Fas和FasL的表达,促进小鼠脾淋巴细胞凋亡。
Objective:This thesis evaluates the pharmacological effects of experienced prescription of the wind Yangxue drink on acute and chronic ACD from the perspective of pathological changes and histomorphology by adopting mice of acute and chronic allergic contact dermatitis(ACD) model,probes immunological mechanism on the level of cells and molecules by examines the relevant cells and its mRNA,so that to provide objective basis for the application of this experience experienced prescription's better prevention and treatment of acute and chronic ACD clinically.
     Materials and Methods
     1.Experimental materials
     (1) Experimental animals:Healthy male Kunming mice.
     (2) Experimental medicine:The method of oral drug delivery is used.The experienced prescription of Yangxue Xiaofeng Drink is adopted in Chinese medical treatment and the control group of Western medicine used loratadine tablets,dissolved with distilled water made turbid liquid;blank group,model group gavage with distilled water contour.
     2.Research Methods
     (1)Model approach:To use the methods of DNCB skin to prepare acute and chronic ACD animal models of mice.
     (2)To make preliminary evaluation of effect of ACD- inhibition by observing the Yangxue Xiaofeng Drink on acute and chronic ACD ear swelling disease in mice,the percentage of swelling inhibition,and spleen index and thymus index.
     (3)To analyze the effects of Yangxue Xiaofeng Drink on acute acute lesions histomorphology through the light microscope and transmission electron microscopy observation of Yangxue Xiaofeng Drink lesions of acute ACD in mice and the pathological changes in tissue ultrastructure.
     (4)To determine the levels of IFN-γand IL-4 in the serum of ACD mouse model by using ELISA method,using RT-PCR used to detect lesions local IFN-γmRNA,IL-4mRNA expression and serum cytokine protein expression and mRNA expression in lesions of the correlation analysis,from the Th1 / Th2 cytokine balance in the perspective of the network to explore further in-depth Yangxue Xiaofeng Drink ACD drink immunological inhibition mechanism.
     (5)To detect content of TNF-α,NF-κBp50,Fas / Fas-L of chronic lesions of cytokines in ACD mouse model by using immunohistochemical methods,and explore the possible role of drinking wind mechanisms and links by studying the pathogenesis of chronic skin lesions of ACD positions cytokine expression in the above-mentioned changes in consumer Yangxue.
     (6)To study the percentage of early apoptosis by Annexin V-FITC apoptosis detection method. and using flow cytometry in chronic ACD mouse spleen lymphocytes,and to explore whether drinking Yangxue Xiaofeng Drink reduced intensity of immune response,thereby inhibiting the occurrence of ACD from cell level by inducing lymphoid ways of apoptosis.
     Results
     1.Yangxue Xiaofeng Drink can reduce acute and chronic ear disease model mice ACD weight difference and swelling degree.
     Acute and chronic ACD model of the ears of mice were significantly higher than the weight difference between the blank group(P<0.01),Yangxue Wind-drink low-,medium-, high-dose group and the group of loratadine ear weight difference with the model group were significantly reduced compared to(P<0.01 or P<0.05).With the range of this experiment dose used,Yangxue Xiaofeng Drink on the role of acute ACD model no significang amount- effect dependence on the role of chronic ACD model was a certain amount - effect dependence.
     2.Yangxue Xiaofeng Drink can be reduced acute and chronic mouse model of ACD spleen index and thymus index.
     Acute and chronic ACD model group mice spleen index,thymus index were significantly higher(P<0.01):Yangxue Xiaofeng Drinking group and loratadine can be significantly reduced acute and chronic mouse model of ACD and the spleen index Thymus index(P<0.01);Yangxue Xiaofeng Drink on the impact of both showed a certain amount - effect dependence.
     3.Yangxue Xiaofeng Drinking mice reduce acute ACD partial lesion histopathology and ultrastructure of the extent of injury
     The mice back skin biopsy of ACD model group showed:loss of partial necrosis of epidermal cells,the cells edema;dermal papilla edema,dermal infiltration of inflammatory cells in large numbers;gap widened collagen fibers;vasodilator,endothelial cell swelling. After the intervention of Yangxue Xiaofeng Drink,the basic structure of full-thickness skin integrity,cells and intercellular edema significantly reduced and inflammatory cell infiltration in the dermis decreased significantly.All levels of damage are less than those of the ACD model group.The number of dermal inflammatory cell infiltration in Loratadine group is more than that of Yangxue Xiaofeng Drink group,and other changes is about the same with Yangxue Xiaofeng Drink group.
     In the study of ultrastructure of the skin,basal cell skin lesions and spine cells of ACD mouse model shrink and the electron density of epidermal keratinocyte slightly enhanced, inter-connection of epidermal basal cells disappear and within the cell,cytoplasm was vacuolated changes nuclear heterochromatin condensed into a mass distribution to the nuclear periphery.The lesions basal cell skin and spine cells of Yangxue Xiaofeng Drinking mice kept structural integrity,cells with mild atrophy,intercellular is liked with desmosomes and the nuclear chromatin basically uniform distribution.Mitochondria and rough endoplasmic reticulum are of structure integrity,little vacuolization,and cell injury is less than the model group.Loratadine group part of the nuclear chromatin was mass distribution,and other changes is about the same with Yangxue Xiaofeng Drink group.
     4.Yangxue Xiaofeng Drink can raised level of IL-4 and reduced levels of IFN-γin serum of ACD model,while increase expression level of of IL-4mRNA reduced the expression level of IFN-γmRNA in ear tissue.
     Levels of IFN-γsignificantly increased in serum of chronic ACD mouse model and the level of IL-4 decreased significantly(P<0.01),there is high expression level of IFN-γmRNA in ear lesions organizations and expression level of IL-4mRNA reduced expression(P<0.01).The ratio of serum IFN-γ/IL-4 ear tissues were significantly higher IFN-γmRNA/IL-4mRNA ratio(P<0.01) in model mice group;Both Yangxue Xiaofeng Drink and loratadine ACD in mice significantly reduced serum levels of IFN-γas well as the ear tissue of IFN-γmRNA expression level(P<0.01);Yangxue Xiaofeng Drink can significantly increase serum IL-4 levels(P<0.05) as well as the ears tissue expression of IL-4mRNA level (P<0.01),while loratadine increase serum levels of IL-4 on the ear lesion tissue expression of IL-4mRNA the level of no effect;Yangxue Xiaofeng Drink or loratadine group,while the impact of the ratio of IFN-γ/IL-4 is of no significant difference between the two groups.
     5.Yangxue Xiaofeng Drink ACD significantly reduced expression levels of TNF-α.and NF-κBp50 in chronic skin lesions of mice,and markedly increase that of Fas and FasL. TNF-αand NF-κBp50 expression were significantly increased(P<0.01) in chronic ear organizations of ACD mouse model;Yangxue Xiaofeng Drink organizations can significantly lower TNF-α,NF-κBp50 expression(P<0.01);TNF-αexpression was not obvious(P>0.05) in tissue of Loratadine group,but can significantly reduced NF-κBp50 expression(P<0.05); and the interference role of Yangxue Xiaofeng Drink is superior to that of loratadine group(P<0.05 or P<0.01).
     Fas and FasL expression were significantly increased(P<0.01) in chronic ear organizations of ACD mouse model;Yangxue Xiaofeng Drink organizations can significantly increase Fas and FasL expression(P<0.01);and loratadine group has no significant effects on the two(P>0.05).
     TNF-αand NF-κBp50,Fas and Fas-L expression in ear skin of mice were positively correlated(correlation coefficients were:0.783,P<0.01;0.747,P<0.01).
     6.Yangxue Xiaofeng Drink chronic drinking can significantly promote the ACD mouse spleen T lymphocytes in early apoptosis.
     Percentage of early apoptosis of lymphocytes is significantly increased in the spleen of model of mouse(P<0.01);Yangxue Xiaofeng Drink or loratadine may significantly increase percentage of early apoptosis of lymphocytes in the mouse spleen,Yangxue Xiaofeng Drinking group was stronger than the loratadine group(P<0.01).
     Percentage of early apoptosis of lymphocytes in Mouse spleen and Fas.Fas-L expression in mouse ears organizations were positively correlated(correlation coefficients were:0.783.P<0.01;0.785,P<0.01).
     Conclusion:
     1.Yangxue Xiaofeng Drink has inhibition effect on acute and chronic ACD of mice and can reduce the swelling of the ear,inhibit the swelling response of immune organs in the course of changes and reduce thymus index and spleen index.
     2.Yangxue Xiaofeng Drink can effectively reduce the injury degree of ultrastructure and local tissue pathological lesions of acute ACD group in mice.
     3.Yangxue Xiaofeng can lower the cytokine of Th1 and promote the secreting of the cytokine of Th2,so that adjust network Th1/Th2 balance of mouse model of chronic ACD.
     4.Yangxue Xiaofeng Drink can significantly lower the TNF-α,NF-κBp50 expression levels in skin lesions of chronic ACD mice,and may inhibit inflammation at the transcriptional level and suppress immune response.
     5.Yangxue Xiaofeng Drink can significantly promote Fas / FasL expression level in the Fas / FasL expression level and promote apoptosis of lymphocytes in mouse spleen.
引文
[1]宋智琦,林熙然.不同类型钙通道阻滞剂对小鼠变应性接触性皮炎及表皮郎格罕细胞的影响.中国皮肤性病学杂志.1998,12(3):137-139.
    [2]陈妍,郭在培.咪唑斯汀抑制小鼠变应性接触性皮炎机制的研究.中华皮肤科杂志.2004,37(6):44-346.
    [3]林熙然,涂彩霞.Ⅳ型变态反应中药治疗湿疹的研究.中国中西医结合杂志.200020(4):258-260.
    [4]陈晶,何春涤,王雅坤等.咪唑斯汀等几种抗组胺药对小鼠接触性皮炎作用的实验研究.临床皮肤科杂志.2005,34(3):154-156.
    [5]杨保华,陈德宇,肖顺汉.消风胶囊对小鼠迟发型超敏反应的影响及其作用机理研究.中国中西医结合皮肤性病学杂志.2003,2(1):13-15.
    [6]王国江,顾军.小鼠背部变应性接触性皮炎模型的建立.中国职业医学.2004 31(1):17-19.
    [7]戴宇飞,牛勇,冷曙光等.三氯乙烯致皮肤过敏动物模型的建立.中华预防医学杂志.2005,39(1):55.
    [8]郭丽芳,范卫新,汤爱民.两种变应原致小鼠变应性接触性皮炎的研究.中华皮肤科杂志.2005,38(4):229-231.
    [9]Boyera N,Caver D,Bouclier M,et al.Reperater application of dinitrochlorobenze to the ears of sensitized guinea pigs:Apreliminary characterization of a potential new animal model for contact eczema in humans.Skin Pharmacol.1992,5(3):185.
    [10]Hiroichi Nagai,Yo shi fu mi Ueda.Different role of IL-4 in the onset of hapten-induced contact hypersensitivity in BALB/c and C57BL/6 mice.Br.J.Pharmacol.2000,129(2):299-306.
    [11]金慧玲,张汝芝,余其斌.小鼠慢性皮炎-湿疹模型的建立.蚌埠医学院学报.2002,27(3):193-194.
    [12]李莉,罗仁,曾抗等.加味玉屏风颗粒对变应性接触性皮炎小鼠模型的干预及对T 细胞分化的影响.南方医科大学学报.2006,26(5):701-702.
    [13]郑咏秋,戴敏,陈光亮等.消风散颗粒抗过敏作用及其机制研究.中国实验方剂学杂志.2002,8(6):26-28.
    [14]李国忠,郑咏秋.消风散颗粒免疫调节作用机理研究.中国实验方剂学杂志.2004.10(4):39-42.
    [15]梁秀宇,关洪全.消风散对Ⅳ型超敏反应中IL-4、IFN-γ及sIL-2R的影响.中国中医药信息杂志2007,14(4):37-38.
    [16]熊恺轩,曾耀英,蔡小嫦等.喘可治注射液抑制小鼠变应性接触性皮炎的实验研究.中国病理生理杂志.2005,21(4):757-760.
    [17]连莉阳,李治牢,聂爱迪.乌蛇败毒胶囊对接触性皮炎小鼠血清IL-2、TNF-α的影响.陕西中医学院学报.2007,30(2):39-41.
    [18]宋瑜,李咏梅,马绍尧等.除湿止痒合剂对变应性接触性皮炎小鼠模型TH1/TH2相关细胞因子水平的影响.成都中医药大学学报.2008,31(1):32-33.
    [19]尤立平,刘永生,刘东玉.皮炎煎剂对小鼠实验性接触性皮炎的疗效及作用机制研究.北京中医药大学学报.2004,27(6):50-52.
    [20]佘鸿燕,王见宾,刘福来.复方马齿苋液对小鼠实验性接触性皮炎的疗效及作用机理研究.中国实用医药.2007,2(27):30-31.
    [21]黄磅,吴铁,樊翌明.6种中药抑制二硝基氟苯小鼠接触性皮炎的实验研究.现代中西医结合杂志.2007,16(13):1756-1757.
    [22]梁秀宇,关洪全,刘文力等.常用清热类中药抗Ⅳ型超敏反应的实验研究,中医药学刊.2006,24(6):1053-1054.
    [23]王丹丹,李维.大黄素对小鼠变态反应性接触性皮炎的作用.广东医学院学报.2008,26(1):14-15.
    [24]陈保疆,王萍,李晓莉等.雷公藤甲素对体外培养的变应性接触性皮炎小鼠Th细 胞Fas表达的影响.时珍国医国药.2008,19(2):443-444.
    [25]FuchibeK,Nabe T,FujiiM,et al.Delayed type allergic itch-asso-ciated response induced by toluene-2,4 -diisocyanate in hairlessmice.J PharmacolSci.2003,93(1):47-54.
    [26]Scholzen TE,Stander S,RiemannH,et al.Modulation of cutaneous inflammation by angiotensin - converting enzyme.J Immunol.2003,,170(7):3866-3873.
    [27]Ohmura T,Tsunenari I,HavashiT,et al.Role of substance P in an NC/Ngamousemodel of atopic dermatitis-like disease.IntArch Allergy Immuno l.2004,133(4):389-397.
    [28]Andoh T,KuraishiY..Nitric oxide enhances substance P- induceditch-associated responses inmice.Br J Pharmacol.2003,138(1):202-208.
    [1]欧阳恒,杨志波,向亚平.湿疹的诊断与治疗.北京:人民军医出版社,2004:4.
    [2]王侠生,廖康煌.杨国亮皮肤病学.上海:上海科学技术文献出版社,2005:78,389-394.
    [3]Walsh GM,Annunziato L,Frossard N,et al.New insights into the second generation antihistanmines.Drugs,2001,61:207-36.
    [4]黄礴,吴铁,樊翌明.6种中药抑制二硝基氟苯所致小鼠接触性皮炎的实验研究.现代中西医结合杂志.2007,16(13):1756-1757.
    [5]梁秀宇,关洪全,刘文力等.常用清热类中药抗Ⅳ型超敏反应的实验研究.中医药学刊.2006,24(6):1052-1054.
    [6]芦源,刘鸿慧,田静.养血消风饮治疗颜面再发性皮炎的临床观察.辽宁中医杂志.2009,36(4):589-590.
    [7]陈奇主编.中药药理研究方法学.北京:人民卫生出版社,1993:1103.
    [8]徐叔云,卞如濂,陈修.药理实验方法学.北京:人民卫生出版社,1997:1430-1432.
    [9]金慧玲,张汝芝,余其斌.小鼠慢性皮炎-湿疹模型的建立.蚌埠医学院学报.2002,27(3):193-194.
    [10]陈平雁主编.SPSS13.0统计软件应用教程.北京:人民卫生出版社,2005:132-125.
    [11]林熙然,涂彩霞,杨春梅等.抗变态反应中药治疗湿疹的研究.中国中西医结合杂志.2000,20(4):258-260.
    [12]谢文平.养血止痒片治疗血虚风燥型慢性湿疹的实验与临床研究:博士学位论文.广州:广州中医药大学,2002
    [13]Boyera N,Caver D,Bouclier M,et al.Reperater application of dinitrochlorobenze to the ears of sensitized guinea pigs:Apreliminary characterization of a potential new animal model for contact eczema in humans.Skin Pharmacol.1992,5(3):185.
    [14]王国江,顾军.小鼠背部变应性接触性皮炎模型的建立.中国职业医学.2004,31(1):17-19.
    [15]Boyera N,Cavey D,Bouclier M,et al.Repeated application of dinitroc hlorobenzene to the ear of sensitized guinea pigs:a preliminary characturization of a potential new animal model for contacteczema in humans.Skin Pharmacol.1992,5(3):184-188.
    [16]Miyauchi H,Horio T.A new animal model for contact dermatitis:the hair less guinia pig.J Dermatol.1992,19(3):140-145.
    [17]李林峰,施辛,王文慧等.皮炎湿疹的发病机制.北京:人民军医出版社,2006:54-63.
    [18]陈锡唐.实用皮肤组织病理学.广州:广东科技出版社,1993:56-59.
    [19]高俊峰.医用组织细胞学电镜图谱.沈阳:辽宁教育出版社,1993:117-124.
    [20]高天文.现代皮肤组织病理学.北京:人民卫生出版社,2001:10-12.
    [21]朱学骏.皮肤的组织病理诊断.北京:北京医科大学、中国协和医科大学联合出版社,1990:132-134.
    [22]陈辉,何立,宗红英.日本血吸虫感染新模型小鼠IFN-γ及IL-4mRNA的动态变化.中国人兽共患病学报.2008,24(4):316-318
    [23]Cumberbatch M,Kimber I.Tumour necrosis factor-α is required for optimal contact require signals from both tumour necrosis factor-a and interleukin-1 β for migration.Immunol.1997,92:388- 395.
    [24]Kidd P.Th1/Th2 balance The hypothesis its limitations ans inplications for health and diseases.Altem Med Rev.2003,8:223-246.
    [25]窦肇华,张远强,郭顺根.细胞和分子免疫学.北京:中国医药科技出版社,2004:396-409,48-49,75
    [26]Leung DY,Boguniewicz M,Howell MD,et al.Newinsights into atopicdermatitis.J Clin Invest,2004,113(5):651-657.
    [27]赵武述.免疫平衡研究及其临床意义.北京:科学出版社,2005:90-106,183-185.
    [28]Wakabayashi T,Hu DL,Tagawa Y,et al.IFN-gamma and TNF-alpha are involved in urushiol-induced contact hypersensitivity in mice.Immunol Cell Biol.2005,83(1):18-24.
    [29]Carroll,J.M.,T.Crompton,J.P.Seery,and F.M.Watt.Transgenic mice expressing IFN- gamma in the epidermis have eczema,hair hypopigmentation,and hair loss.[J].J Invest Dermatol.1997,108:412-422.
    [30]龚非力.医学免疫学.北京:科学出版社,2005:148-314.
    [31]Nakamura T,,Lee R K,,Nam S Y,et al.Roles of Ih-4 and IFNgamma in stabilizing the T helper cell type 1 and 2 phenotype.Immurol.1997,158(6):2648-2653.
    [32]Mosmann & S Sad.The expanding universe of T-cell subsets:Th1,Th2 and more.Immunol Today.1996,17:142-46.
    [33]Grabbe S,Schwarz T.hnmunoregulatory mechanisms involved in elicitation of allergic contact hypersensitivity.Immunol Today.1998,19:37-44.
    [34]Bell S,Degitz K,Quirling M etal.Involvent of NF-kappaB signalling in skin physiology and disease.Cell Signal.2003,15:1-7.
    [35]Westphal GA,Schnuch A,Moessner R,et al.Cytokine gene polymorphisms in allergic contact dermatitis.Contact Dermatitis.2003,48:93-98.
    [36]Karin M.Nuclear factor-κB in cancer development and progression.Nature.2006,441(7092):431-436.
    [37]Baldwin AS.The NF-kappa B and I kappa B Protein:new disceoveries and insights.AnnuRev Immunol.1996,14:649-683.
    [38]朱桂英,徐斌,张捷,等.TNF-α活化人瘢痕疙瘩成纤维细胞NF-κB的实验研究.中国病理生理杂志.2008,24(1):165-168.
    [39]鲍国强,章扬培.NF-κB的生物学功能.国外医学分子生物学分册.2003,25(6):345-348.
    [40]陈慰峰主编.医学免疫学.北京:人民卫生出版社,2006:155-156.
    [41]胡野,凌志强,单小云.细胞凋亡的分子医学.北京:军事医学科学出版社,2004:21,76-81,153-158,251-252,390-396.

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