期刊文献+

血清HO-1水平在获得性噬血细胞综合征中的临床意义探讨 被引量:6

Discussion about the clinical significance of the levels of serum HO-1 in hemophagocytic syndrome
下载PDF
导出
摘要 目的探讨血清血红素氧合酶-1(HO-1)升高在获得性噬血细胞综合征(HPS)中的诊断价值及监测其病情变化的临床意义,为临床诊疗工作的进一步开展提供理论依据。方法收集首都医科大学附属北京友谊医院2012年3月至2013年5月期间收治的HPS疑似患者129例,根据HLH-2004诊断标准最终分为原发性HPS患者8例,确诊获得性HPS组65例,排除组56例。并选取健康志愿者27例,采用酶联免疫吸附法检测所有获得性HPS患者确诊时、排除组患者、健康志愿者及部分获得性HPS临床治疗有效患者治疗2周后血清HO-1浓度,比较各组间差异。结果获得性HPS确诊组患者血清HO-1浓度明显高于排除组及正常实验对照组(F=36.835,P=0.000)。自身免疫性疾病相关性HPS血清HO-1浓度高于感染相关性HPS及淋巴瘤相关性HPS患者,组间比较差异具有统计学意义(F=4.579,P=0.014)。监测36例获得性HPS临床治疗有效患者治疗2周后血清HO-1浓度发现,治疗后血清HO-1浓度明显降低,差异有统计学意义(t=2.536,P=0.01)。血清HO-1与NK细胞活性、可溶性白细胞介素-2受体(sCD25)均无明显相关性;与铁蛋白有一定相关,但相关系数较小(r=0.273,P=0.028)。结论血清HO-1在获得性HPS患者中明显升高,尤其在自身免疫性疾病相关性HPS患者中明显高于淋巴瘤相关性HPS及感染相关性HPS,这对于诊断自身免疫性疾病相关性HPS具有重要提示意义,HO-1有可能成为监测获得性HPS病情变化的重要指标。 Objective To explore the diagnostic value and the clinical significance of monitoring the condition changes of serum HO - 1 in acquired hemophagocytic syndrome ( HPS), so as to provide a theoretical basis for the further development of clinical work. Methods Relevance data of 129 suspected I-IPS patients in Beijing Friendship Hospital, Capital Medical University were collected during the period from March 2012 to May 2013. All these patients were divided into three groups according to HLH -2004 diagnostic criteria, including 8 primary HPS patients, 65 di- agnosed acquired HPS patients and other 56 excluded person. 27 healthy volunteers were included into this study. The level of serum HO - 1 of all the person and some patients with acquired HPS were detected. All these subjects had 2 weeks effective clinical treatment. The serum HO - 1 level of these subjects were compared among the different groups. Results The serum HO - 1 levels of patients with acquired HPS were significantly higher than those of two other groups ( F = 36. 835, P = 0. 000). The serum HO - 1 levels of autoimmune disease associated hemophagocytic syn- drome were higher than those of infection associated HPS and lymphoma associated hemophagoeytie syndrome, with statistical significance ( F = 4. 579, P = 0. 014). The serum HO - 1 of 36 patients with acquired HPS who had 2 weeks effective clinical treatment were monitored. The serum HO - 1 levels were significantly lower after treatment . The difference was statistically significant ( t = 2. 536, P = 0.01 ). There was no correla- tion between Serum HO - 1, NK cell activity and sCD25. Ferritin had some relevance with HO - 1, but the correlation coefficient is small ( r = 0. 273, P = 0. 028 ). Conclusion The serum HO - 1 in patients with acquired HPS significantly increased, especially in the autoimmune disease associated hemophagoeytic syndrome, which had important signifleance for the diagnosis of autoimmune diseases associated HPS. The serum HO - 1 may be an important indicato
出处 《临床和实验医学杂志》 2013年第20期1609-1611,共3页 Journal of Clinical and Experimental Medicine
基金 国家自然科学基金(81270653) 首都医学发展科研基金(2009-1032) 北京市科技计划首都临床特色应用研究(D101100050010005) 中华医学会关于临床医学科研专项资金(11010020246) 北京友谊医院科研启动基金(YYQDKT2011-6)
关键词 噬血细胞综合征 HO-1 酶联免疫吸附测定 Hemophagocytic syndrome HO - 1 Enzyme - linked immunosorbent assay
  • 相关文献

参考文献9

二级参考文献60

  • 1Tenhunen R,Marver HS,Schmid R.Microsomal heme oxygenase:characterization of the enzyme[J].J Biol Chem,1969,244(23):6388-6394. 被引量:1
  • 2Stocker R.Induction of heme oxygenase as a defense against oxidative stress[J].Free Rad Res Commun,1990,9(4):101-112. 被引量:1
  • 3Lee PJ,Alam J,Sylvester SL,et al.Regulation of heme oxygenase-1 expression in vivo and in vitro in hyperoxic lung injury[J].Am J Respir Cell Mol Biol,1996,14(6):556-568. 被引量:1
  • 4Rensing H,Jaeschke H,Bauer I,et al.Differential activation pattern of redox-sensitive transcription factors and stress-inducible dilator systems heme oxygenase-1 and inducible nitric oxide synthase in hemorrhagic and endotoxic shock[J].Crit Care Med,2001,29(10):1962-1971. 被引量:1
  • 5Yang ZZ,Zou AP.Transcriptional regulation of heme oxygenase by HIF-1α in renal medullary interstitial cells[J].Am J Physiol Renal Physiol,2001,281(5):F900-F908. 被引量:1
  • 6Lu TH,Lambrecht RW,Pepe J,et al.Molecular cloning,characterization,and expression of the chicken heme oxygenase-1 gene in transfected primary cultures of chick embryo liver cells[J].Gene,1998,207(2):177-186. 被引量:1
  • 7Sethi JM,Otterbein LE,Choi AM.Differential modulation by exogenous carbon monoxide of TNF-α-stimulated mitogen activated protein kinase signaling in rat pulmonary artery endothelial cells[J].Antioxid Redox Signal,2002,4(2):241-248. 被引量:1
  • 8Ferris CD,Jaffrey SR,Sawa A,et al.Haem oxygenase-1 prevents cell death by regulating cellular iron[J].Nat Cell Biol,1999,1(3):152-157. 被引量:1
  • 9Petrache IL,Otterbein E,Alam J,et al.Heme oxygenase-1 inhibits TNF-α-induced apoptosis in cultured fibroblasts[J].Am J Physiol Lung Cell Mol Physiol,2000,278(2):L312-L319. 被引量:1
  • 10Brouard S,Otterbein LE,Anrather J,et al.Carbon monoxide generated by heme oxygenase-1 suppresses endothelial cell apoptosis[J].J Exp Med,2000,192(7):1015-1026. 被引量:1

共引文献86

同被引文献75

  • 1Zur S U, Beutel K, Kolberg S, et al.Mutaion spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses ofPRF1, UNC13D, STX11 and RAB27A[J].Hum Murat, 2006, 27 ( 1 ) : 62-68. 被引量:1
  • 2Stepp S E, Dufourcq-Lagelouse R, Le D F, et al.Perforin gene defects in familial hemophagocytic lymphohistiocytosis[J].Science, 1999, 286 (5446) : 1957-1959. 被引量:1
  • 3Schmid J P, Cote M, Menager M M, et al.Inherited defects in lymphocyte cytotoxic activity[J].Immunol Rev, 2010, 235 (6) : 10- 23. 被引量:1
  • 4Ueda I, Ishii E, Morimoto A, et al.Correlation between phenotypic heterogeneity and gene mutational characteristics in familial hemophagocytic lymphohistiocytosis ( FHL ) [J].Pediatr Blood Cancer, 2006, 46 ( 4 ) : 482-488. 被引量:1
  • 5Voskoboinik I, Dunstone M A, Baran K, et al.Perforin: structure, function, and role in human immunopathology[J].Immunol Rev, 2010, 235 (16) : 35-54. 被引量:1
  • 6Feldmann J, Callebaut I, Raposo G, et al.Muncl3-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis ( FHL3 ) [J].Cell, 2003,115 ( 4 ): 461-473. 被引量:1
  • 7Zur S U, Schmidt S, Kasper B , et al.Linkage of familial hemophagocytic lymphohistiocytosis ( FHL ) type-4 to chromosome 6q24 and identification of mutations in syntaxin 1 l[J].Hum Mol Genet, 2005, 14 ( 6 ) : 827-834. 被引量:1
  • 8Zur S U, Rohr J, Seifert W, et al.Familial hemophagocytic lymphohistiocytosis type 5 ( FHL-5 ) is caused by mutation in Muncl8-2 and impaired binding to syntaxin 11[J].Am J Hum Genet, 2009, 85 ( 4 ) : 482-492. 被引量:1
  • 9Munson M, Hughson F M.Conformational regulation of SNARE assembly and disassembly in vivo[J].J Biol Chem, 2002, 277 ( 11 ) : 9375-9381. 被引量:1
  • 10Mamishi S, Modarressi M H, Pourakbari B, et al.Analysis of RAB27A gene in griscelli syndrome type2: novel mutations including a deletion hotspot[]].J Clin Immunol, 2008, 28 ( 4 ) : 384-389. 被引量:1

引证文献6

二级引证文献12

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