期刊文献+

不同剂量致敏原对小鼠过敏性哮喘模型特异性抗体和炎性细胞因子的影响 被引量:2

Influence of different dose of sensitinogen on serum specific antibody and inflammatory cytokines in allergic asthma model in mice
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摘要 目的 观察不同剂量致敏原对小鼠过敏性哮喘模型血清特异性抗体IgE、IgG2a和白细胞介素-4(IL-4)、白细胞介素-5(IL-5)、白细胞介素-12(IL-12)、γ-干扰素(IFN-γ)等炎性细胞因子的影响.方法 45只雌性BALB小鼠随机分为4组,空白对照组腹腔注射不含鸡卵蛋白(OVA)的PBS缓冲液,低、中、高剂量组分别注射含10、100、1 000 μg OVA的PBS缓冲液,第15 ~20天以雾化吸入OVA生理盐水激发致敏,制备过敏性哮喘模型.结果 各给药组均出现不同程度炎细胞浸润,低剂量组最为显著;低、中、高剂量组血清IgE、IL-4、IL-5水平呈递减趋势,组间差异显著(P<0.01),且均显著高于对照组(P<0.01);各实验组血清IgG2a、IL-12及IFN-γ水平呈递增趋势,组间差异显著(P<0.01),且与对照组差异显著(P<0.05或P<0.01).结论 不同剂量的OVA可能影响小鼠过敏性哮喘模型所产生的细胞因子类型,低剂量OVA造模的效果最为显著,高剂量OVA可能导致小鼠发生免疫耐受. Objective To observe the influence of different dose of snetitinogen on IgE, IgG2a, IL-4, IL-5, IL-12 and IFN-γ in allergic asthma model in mice. Methods A total of 45 female BALB mice were divided into 4 groups, of which blank control group was given intraperitoneal injection of PBS buffer solution not containing OVA while low, middle and high dose groups were injected PNS buffer solution containing 10, 100 and 1 000 p.g OVA, respectively. Allergic asthma models were prepared by aerosol inhalation of OVA normal saline (NS) for sensitization. Results Different degree of inflammatory cell infiltration appeared in medication administration groups, and most obvious in low-dose group. IgE and IL-4 and IL-5 levels in low, middle and high dose groups showed a trend of decline and were significantly higher than those of control group (P 〈 0.01). IgG2a, IL-12 and IFN-γ levels showed a increasing trend and there were significant differences among groups ( P 〈 0.05, or P 〈 0.0O1 ). Conclusion Different dose of OVA may affect cytokine type caused by allergic asthma model in mice, and high-dose OVA might lead to immune tolerance in mice.
出处 《实用临床医药杂志》 CAS 2014年第21期8-11,共4页 Journal of Clinical Medicine in Practice
基金 中国高校医学期刊临床专项资金(11321443)
关键词 致敏原 过敏性哮喘 白细胞介素-4 白细胞介素-5 肿瘤坏死因子-γ 细胞因子 sensitinogen interleukin-4 interleukin-5 tumor necrosis factor-γ eytokines
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参考文献13

  • 1Busse W W,Morgan W J,Gergen P J,et al.Randomized trial of omalizumab(anti-Ig E)for asthma in inner-city children[J].New England Journal of Medicine,2011,364(11):1005.
  • 2Jin C,Shelburne C P,Li G,et al.Particulate allergens potentiate allergic asthma in mice through sustained Ig E-mediated mast cell activation[J].The Journal of clinical investigation,2011,121(3):941.
  • 3Huang X,Tang L,Wang F,et al.Astragaloside IV attenuates allergic inflammation by regulation Th1/Th2 cytokine and enhancement CD4+CD25+Foxp3 T cells in ovalbumin-induced asthma[J].Immunobiology,2014,219(7):565.
  • 4商艳,李强,黄怡,白冲,刘忠令.不同剂量致敏原对小鼠过敏性哮喘模型的影响[J].第二军医大学学报,2002,23(1):69-71. 被引量:23
  • 5樊卫文,杨志军,孙滨,孙秉中.过敏性哮喘大鼠大脑和肺组织c-fos蛋白的表达[J].中华结核和呼吸杂志,2001,24(8):469-471. 被引量:5
  • 6Arnold I C,Dehzad N,Reuter S,et al.Helicobacter pylori infection prevents allergic asthma in mouse models through the induction of regulatory T cells[J].The Journal of clinical investigation,2011,121(8):3088.
  • 7Ather J L,Ckless K,Martin R,et al.Serum amyloid A activates the NLRP3 inflammasome and promotes Th17 allergic asthma in mice[J].The Journal of Immunology,2011,187(1):64.
  • 8吴静,胡东,李朝品,张荣波.细菌内毒素对粉尘螨诱导的哮喘小鼠肺部炎症的免疫调节[J].中华微生物学和免疫学杂志,2007,27(12):1132-1135. 被引量:7
  • 9Abrahamsson T R,Sandberg Abelius M,Forsberg A,et al.A Th1/Th2 associated chemokine imbalance during infancy in children developing eczema,wheeze and sensitization[J].Clinical&Experimental Allergy,2011,41(12):1729.
  • 10Zhao Y,Yang J,Gao Y D.Altered expressions of helper T cell(Th)1,Th2,and Th17 cytokines in CD8+andγδT cells in patients with allergic asthma[J].Journal of Asthma,2011,48(5):429.

二级参考文献36

  • 1胡东,张荣波.小鼠过敏性哮喘模型发病机制研究进展[J].现代预防医学,2007,34(2):300-301. 被引量:3
  • 2胡东,张荣波,吴静.居室内毒素含量与儿童过敏性哮喘相关性调查[J].中华流行病学杂志,2007,28(4):354-357. 被引量:4
  • 3孙秀珍 米烈汉.西安地区蛾致敏原的调查及临床研究[J].西安医科大学学报,1996,12:34-36.
  • 4[1]Watson ML,White AM,Campbell EM,et al.Anti-inflammatory actions of interleukin-13:suppression of tumor necrosis factor-alpha and antigen-induced leukocyte accumulation in the guinea pig lung[J].Am J Respir Cell Mol Biol,1999,20(5):1007-1012.
  • 5[2]Shim JJ, Dabbagh K,Takeyama K, et al.Suplatast tosilate inhibits goblet-cell metaplasia of airway epithelium in sensitized mice[J].J Allergy Clin Immunol,2000,105(4):739-745.
  • 6[3]Zhao GD, Yokoyama A,Kohno N, et al .Effect of suplatast tosilate (IPD-1151T) on a mouse model of asthma:inhibition of eosinophilic inflammation and bronchial hyperresponsiveness[J].Int Arch Allergy Immunol,2000,121(2):116-122.
  • 7[4]Zuhdi AM,Piazza FM,Selby DM, et al.Muc-5/5ac mucin messenger RNA and protein expression is a marker of goblet cell metaplasia in murine airways[J].Am J Respir Cell Mol Biol,2000,22(3):253-260.
  • 8[5]Constant S, Pfeiffer C,Woodard A.Extent of T cell receptor ligation can determine the functional differentiation of naive CD4+ T cells[J].J Exp Med,1995,182(5):1591-1596.
  • 9[6]Temann UA, Prasad B,Gallup MW, et al.A novel role for murine IL-4 in vivo:induction of MUC5AC gene expression and mucin hypersecretion[J].Am J Respir Cell Mol Biol,1997,16(4):471-478.
  • 10[7]Schwarze J,Hamelmann E, Cieslewicz G, et al.Local treatment with IL-12 is an effective inhibitor of airway hyperresponsiveness and lung eosinophilia after airway challenge in sensitized mice[J].J Allergy Clin Immunol,1998,102(8):86-93.

共引文献59

同被引文献43

  • 1刘晓微,蒋敏,农光民,刘宏涌,彭方,刘静.中性粒细胞性支气管哮喘小鼠模型的建立及其气道高反应规律的研究[J].中华哮喘杂志(电子版),2013,7(3):1-5. 被引量:14
  • 2World Health Organization (homepage on the Intemet) Bronchial Asthma( update 2013 November; Available from http ://www. who. int/mediacentre/factsheets/fs307/en/).
  • 3Shin YS, Takeda K, Gelfand EW. Understanding asthma using animal models [ J ]. Allergy Asthma Immunol Res, 2009,1 (1) :10-18.
  • 4Ghonim MA, Pyakurel K, Ibba SV, et al. PARP inhibition by olaparib or gene knockout blocks asthma-like manifestation in mice by modulating CD4 + T cell function [ J ]. J Transl Med, 2015,13 : 225-236.
  • 5Gabehart KE, Royce SG, Maselli DJ, et al. Airway hyperresponsiveness is associated with airway remodeling but not inflammation in aging Cav lmice[ J]. Respir Res,2013,14: 110-120.
  • 6Ressmeyer A, Larsson AK, Vollmer E, et al. Characterisation of guinea pig precision-cut lung slices: comparision with human tissues [J]. Eur J Respir, 2006,28 : 603-611.
  • 7Murad HA, Hasanin AH. The anti-inflammatory effects of 1,1 dimethyl-4- phenylpiperazinium(DMPP) compared m dexamethasone in a guinea pig model of ovalbumin induced asthma [J]. Eur Rev Med Pharmacol Sci ,2014,18:2228-2236.
  • 8Kobayashi M, Kubo S, Shiraki K, et al. Therapeutic potential of ASP3258, a selective phosphodiesterase 4 inhibitor, on chronic eosinophilic airway inflammation [ J ]. Pharmacology, 2012,90 : 223-232.
  • 9Hylkema M, Hoekstra MO, Luinge M, et al. The strength of the OVA-induced airway inflammation in rats is strain dependent [J]. Clin Exp Immunol,2002,129 ( 3 ) : 390-396.
  • 10Kucharewicz I, Bodzenta-Lukaszyk A, Buczko W. Experimental asthma in rats[J].Pharmacol Rep,2008,60(6) :783-8.

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