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儿童噬血细胞性淋巴组织细胞增生症外周血淋巴细胞亚群分析

Periphery Leukomonocyte Subgroup In children with hemophagocytic lymphohistiocytosis
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摘要 【目的】研究儿童噬血细胞性淋巴组织细胞增生症(hemophagocytic lymphohistiocytosis,HLH)外周血淋巴细胞活性的改变。【方法】选择2005年1月—2009年12月在本院住院的49例确诊为HLH且为急性期的患儿为病例组,30例健康儿童为对照组,分别抽取外周血,肝素抗凝,采用流式细胞术方法分别检测两组外周血淋巴细胞CD3+、CD4+、CD8+、CD(16+56)+的表达率。【结果】病例组CD(16+56)+和CD8+细胞比例显著低于对照组(P<0.01),CD3+细胞比例高于对照组(P<0.05),CD4+细胞比例与对照组比较无显著统计学意义(P>0.05)。【结论】NK细胞[CD(16+56)+]和CTL细胞(CD8+)活性的降低对诊断HLH可能具有重要临床意义,T淋巴细胞(CD3+)活性增强对诊断HLH也有一定价值。 【Objective】 To study the activity changes of Periphery Leukomonocyte in children with hemophagocytic lymphohistiocytosis(HLH).【Methods】 The expression of CD3+、CD4+、CD8+、CD(16+56)+on peripheral blood lym-phocytes of 49 patients with HLH(patients group) and 30 healthy children(control group) were analyzed by flow cytome-try.【Results】 Compared with the control group,the expression of CD(16 + 56)、CD8 were markedly decreased(P 0.01).The expression of CD3 was increased(P0.05).The ratio between CD4+and CD8+was decreased(P 0.05).There was no significant difference on the expression of CD4 between this two groups(P 0.05).【Conclusions】 The decreasing activity of NK cell[(CD16+56)+] and CTL(CD8+) may play an important role in the diagnosis of HLH.The increasing activity of Total T lymphocytes(CD3+) may be valuable on the diagnosis of HLH as well.
出处 《中国儿童保健杂志》 CAS 2010年第12期1008-1010,共3页 Chinese Journal of Child Health Care
关键词 噬血细胞性淋巴组织细胞增生症 儿童 淋巴细胞亚群 hemophagocytic lymphohistiocytosis children lymphocyte subsets
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  • 1汤永民,廖婵.噬血细胞综合征的分子生物学基础及其发病机制[J].实用儿科临床杂志,2006,21(9):513-516. 被引量:11
  • 2Janka GE. Familial and acquired hemophagocytic lymphohistiocytosis. Eur J Pediatr, 2007 ;166:95 - 109
  • 3Kontopoulou T ,Tsaousis G,Vaidakis E, et al. Hemophagocytic syndrome in association with visceral leishmaniasis. Am J Med, 2002; 113:439 -440
  • 4Eguchi K. Systemic lupus erythemalosus complicated by cytomegalovirus-induced hemophagocytic syndrome and colitis. Intern Med, 2002,41:77 - 78
  • 5Janka GE. Familial and acquied hemophagocytic lymphohistiocytosis. Eur J Pediatr, 2007 ; 166:95 - 109
  • 6Henter JI, Elinder G, Ost A. Diagnostic guideline for hemophagocytic lymphohistiocytosis. The FHL Study Group of the Histocyte Society. Semin Onco1,1991 ;18:29 -33
  • 7Henter JI, Home A, Arico M,et al. HLH-2004 : diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer, 2007 ;48 : 124 - 131
  • 8Hercend T, Schmidt RE. Characteristics and uses of natural Killer Ceils. Immunol Today, 1988 ; 9:291 -293
  • 9Menasche G, Feldmann J , Fischer A , et al. Primary hemophagocytic syndromes point to a direct link between lymphocyte cytotoxicity and homeostasis. Immunol Rev, 2005, 203 : 165 - 179
  • 10Takahashi N, Chubachi A, Kume M, et al. A clinical analysis of 52 aduh patients with hemophagocytic syndrome : the prognostic significance of the underlying disease. Int J Hematol,2001 ;74:209 -213

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