期刊文献+

急性免疫性血小板减少症患儿血清IL-33检测及其意义 被引量:3

Serum IL-33 determination in acute immune thrombocytopenia patients and its clinical significance
原文传递
导出
摘要 为研究IL-33在儿童急性免疫性血小板减少症(ITP)发病机制中的作用及意义,我们采用ELISA法检测了37名ITP患儿和37名对照者血清IL-33水平,分析IL-33与患儿就诊时血小板计数及后期疗效的关系。我们发现,ITP患儿血清IL-33较对照者明显增高(P<0.01),且与血小板计数呈负相关(R2=0.10,P=0.05)。血清IL-33水平与治疗效果密切相关,采用IL-33预测ITP患儿疗效,预测敏感性为0.88,特异性为0.81。这些结果提示:IL-33参与了ITP的发病机制,血清IL-33水平可以作为预测患儿疗效的免疫学指标。 To investigate the role of IL-33 in the pathogenesis of acute immune thrombocytopenia(ITP) and its potential clinicalsignificance, the serum IL-33 level in 37 ITP children and 37 healthy controls were detected by ELISA. The correlation between serum IL-33 level and platelet count and therapeutic outcome was analyzed. Increased serum IL-33 level (P〈0.01), which negatively correlated with platelet count (R^2=.10,P=0.05), was observed in ITP children. In addition, increased serum IL-33 was associated with poor therapeutic outcome. Thus it could be used as an effective predictive marker for therapeutic outcome, with a predictive sensitivity of 0.88 and specificity of 0.81. These results suggest that IL-33 involves in the pathogenesis of ITP and could be used as a predictive marker for therapeutic outcome.
机构地区 无锡市人民医院
出处 《现代免疫学》 CAS CSCD 北大核心 2012年第6期506-509,共4页 Current Immunology
关键词 免疫性血小板减少症 IL-33 发病机制 immune thromboeytopenia(ITP) IL-33
  • 相关文献

参考文献13

  • 1Cines DB, Bussel JB, Liebman HA, et al. The ITP syn- drome: pathogenic and clinical diversity[J]. Blood, 2009, 113 :6511-6521.
  • 2Gernsheimer T. Chronic idiopathic thrombocytopenic purpu- ra: mechanisms of pathogenesis[J] Oncologist, 2009, 14: 12-21.
  • 3Sims JE, Smith DE. The IL-1 family: regulators of immunity [J]. Nat Rev Immunol, 2010,10:89-102.
  • 4武燕,柳晓金,李明才.IL-33/ST2信号转导系统及其与疾病关系的研究进展[J].现代免疫学,2010,30(2):164-167. 被引量:4
  • 5Xu D, Jiang HR, Kewin P, etal. IL-33 exacerbates antigen- induced arthritis by activating mast cells[J]. Proc Natl Acad Sci USA, 2008,105 : 10913-10918.
  • 6穆荣,蒋慧蓉,李玉宾,Iain B McIness,栗占国.白细胞介素-33促进胶原诱导性关节炎的实验研究[J].中华风湿病学杂志,2010,14(3):165-167. 被引量:2
  • 7Palmer G, Talabot-Ayer D, Lamacehia C, etal. Inhibition of interleukin-33 signaling attenuates the severity of experimen- tal arthritis[J]. Arthritis Rheum, 2009,60:738-749.
  • 8Yang Z, Liang Y, Xi W, et al. Association of increased ser- um IL-33 levels with clinical and laboratory characteristics of systemic lupus erythematosus in Chinese population[J]. Clin Exp Med, 2011,11:75-80.
  • 9黄鹤卿,穆荣,刘霞,王世瑶,李忆农,栗占国.白细胞介素-33的测定及其与早期类风湿关节炎相关性的研究[J].中华风湿病学杂志,2010,14(7):446-449. 被引量:3
  • 10Yanaba K, Yoshizaki A, Asano Y, etal. Serum IL-33 levels are raised in patients with systemic sclerosis: association with extent of skin sclerosis and severity of pulmonary fibrosis [J]. Clin Rheumatol, 2011,30:825-830.

二级参考文献78

  • 1Dinarello CA. The IL-1 famiLy and inflammatory diseases[J]. Clin Exp Rheumatol,2002,20 ( 5 Suppl 27 ) : S1 -S13.
  • 2Schmitz J, Owyang A, Oldham E ,et al. IL-33, an interleukin-1 -like cytokine that signals via the IL-1 receptor-related protein ST2 and induces T helper type 2-associated cytokines [ J ]. Immunity,2005, 23 (5) :479-490.
  • 3Carriere V, Roussel L, Ortega N, et al. IL-33, the IL-1-like eytokine ligand for ST2 receptor,is a chromatin-associated nuclear factor in vivo[J]. Proc Natl Acad Sci USA,2007,104( 1 ) :282-287.
  • 4Allakhverdi Z, Smith DE, Comeau MR,et al. Cutting edge: the ST2 ligand IL-33 potently activates and drives maturation of human mast cells[J]. J Immunol,2007,179(4) :2051-2054.
  • 5Iikuta M, Suto H, Kajiwata N, et al. IL-33 can promote survival, adhesion and cytokine production in human mast cells [ J ]. Lab Invest ,2007,87(10) :971-978.
  • 6Ali S,Huber M,Koltewe C,et al. IL-1 receptor accessory protein is essential for IL-33-induced activation of T lymphocytes and mast cells[J]. Proc Natl Acad Sci USA,2007,104(47) :18660-18665.
  • 7Ho LH,Ohno T,Oboki K,et al. IL-33 induces IL-13 production by mouse mast cells independently of IgE-FceRI signals[J]. J Leukoc Biol,2007,82 ( 6 ) : 1481-1490.
  • 8Moulin D, Donze O, Talabot-Ayer D, et al. Interleukin ( IL ) -33 induces the release of pro-inflammatory mediators by mast cells [ J ]. Cytokine,2007,40( 3 ) :216-225.
  • 9Trajkovic V ,Sweet MJ ,Xu D. T1/ST2 - an IL-1 receptor-like modulator of immune responses [ J ]. Cytokine Growth Factor Rev, 2004,15(2/3) :87-95.
  • 10Bergem G, Reikerstorfer A, Braselmann S,et al. Alternative promoter usage of the Fos-responsive gene Fit-1 generates mRNA isoforms coding for either secreted or membrane-bound proteins related to the IL-1 receptor [J]. Embo J, 1994,13 ( 5 ) : 1176 - 1188.

共引文献84

同被引文献33

  • 1余上才,章育正,赵慧娟,于丽华.枸杞子和白术免疫调节作用的实验研究[J].上海免疫学杂志,1994,14(1):12-13. 被引量:77
  • 2Baekkevold ES, Roussigne M, Yamanaka T, et al. Molecular charac- terization of NF-HEV, a nuclear factor preferentially expressed in hu- man high endothelial venules [J]. Am J Pathol,2003,163(1):69-79.
  • 3Schrnitz J, Owyang A, Oldham E, et aL IL-33, an interleukin-1-like cytokine that signals via the IL-1 receptor-related protein ST2 and in- duces T helper type 2-associated cytokines [J]. Immunity, 2005,23(5): 479-490.
  • 4Roussel L, Erard M, Cayrol C, et al. Molecular mimicry between IL- 33 and KSHV for attachment to chromatin through the H2A-H2B acidic pocket [J]. EMBO Rep, 2008,9(10): 1006-1012.
  • 5Tominaga S. A putative protein of a growth specific cDNA from BALB/c-3T3 cells is highly similar to the extracellular portion of mouse interleukin 1 receptor [J]. FEBS Lett, 1989,258(2):301-304.
  • 6Pei C, Barbour M, Fairlie-Clarke KJ, et al. Emerging role of interleu- kin-33 in autoimmune disease [J]. Immunology,2014, 141(1):9-17.
  • 7Li XL, Lin TT, Qi CY, et al. Elevated serum level of IL-33 and sST2 in patients with ankylosing spondylitis:associated with disease activi- ty and vascular endothelial growth factor [J]. J Investig Med, 2013,61 (5):848-851.
  • 8Li GX, Wang S, Duan ZH, et al. Serum levels of IL-33 and its recep- tor ST2 are elevated in patients with ankylosing spondylitis [J]. Scand J Rheumatol, 2013,42(3):226-231.
  • 9Ciccia F, Alessandro R, Rizzo A, et al. Macrophage phenotype in the subclinical gut inflammation of patients with ankylosing spondylitis [J]. Rheumatology(Oxford), 2014,53(1): 104-113.
  • 10Han GW, Zeng LW, Liang CX, et al. Serum levels of 1L-33 is in- creased in patients with ankylosing spondylitis [J]. Clin Rheumatol, 2011,3(12):1583-1588.

引证文献3

二级引证文献16

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部