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HCMV感染在小儿特发性ITP中的作用及机制
引用本文:曾耀光,程力平,任志宏. HCMV感染在小儿特发性ITP中的作用及机制[J]. 海南医学院学报, 2013, 0(11): 1585-1588
作者姓名:曾耀光  程力平  任志宏
作者单位:湖北省黄冈市中心医院儿科,湖北黄冈438000
基金项目:中国高校医学期刊临床专项资金项目(112210865)
摘    要:目的:探讨小儿血小板减少性紫癜(ITP)与巨细胞病毒(HCMV)感染的相关性。方法:选取52例ITP患儿为研究对象,根据临床分度将其分为急性型(AITP)21例以及慢性型(CITP)31例,同时选取g0例健康体检儿童为对照组,采用二步免疫组化法测定各组骨髓中HCMV—IgM及采用ELISA免疫法测定各组血清中HCMV—IgM,并对各组临床特点进行分析。结果:AITP组及CITP组骨髓中HCMV阳性率显著血液中HCMV阳性率,差异有统计学意义(P〈0.05);CITP骨髓及血液+HC—MV阳性率均高于AITP及对照组,差异有统计学意义(P〈0.05);AITP及cITP组中骨髓HCMV(+)者平均年龄、IL-6、TNF—a水平均高于骨髓HCMV(-)者,而血小板计数少于HCMV(-),差异有统计学意义(P〈0.05);而CITP组中骨髓HCMV(+)者IL-6、TNF—a水平高于AITP组HCMV(-)者,而血小板计数少于AITP组HCMV(-)者,差异有统计学意义(P〈0.05);AITP及CITP组中血液HCMV(+)者平均年龄、血小板计数、IL-6、TNF—a水平均与血液HCMV(-)者相比,差异无统计学意义(P〉0.05)。结论:骨髓HCMV感染可能是引起ITP发病的重要因素之一。骨髓HCMV感染可能是引起ITP患儿病情加重及慢性化趋向的重要因素,骨髓HCMV感染在ITP患儿发病机制中可能通过破坏患儿免疫系统从而影响血小板的生成,并不是抑制红细胞的生成。

关 键 词:巨细胞病毒  小儿  血小板减少性紫癜  感染

Role and mechanism of HCMV infection in children with idiopathic ITP
ZENG Yao-guang,CHENG Li-ping,REN Zhi-hong. Role and mechanism of HCMV infection in children with idiopathic ITP[J]. Journal of Hainan Medical College, 2013, 0(11): 1585-1588
Authors:ZENG Yao-guang  CHENG Li-ping  REN Zhi-hong
Affiliation:(Department of Pediatrics, Central Hospital of Huanggang City, Hubei Province 438000 China)
Abstract:Objective: To investigate the correlation between ediatric thrombocytopenic purpura (ITP) and cytomegalovirus (HCMV) infection. Methods: A total of 52 ITP patients were divided into a- cute type (AITP)(n=21)and chronic type (CITP) (n=31), besides 30 cases of healthy children were also selects as control group. The bone marrow HCMV-IgM and serum HCMV-IgM were measured with two- step immunohistochemical method and ELISA immunoassay method. The clinical characteristics of each group were also analyzed. Results: In both AITP group and CITP group, positive rate of marrow HCMV rates were higher than the serum HCMV-positive rate (P〈i0.05). Both marrow and serum HCMV-posi- tire rate of the AITP group were higher than that of the control group (P〈0.05). In both AITP and CITP groups, marrow HCMV (+) patients showed older average age, and higher IL-6 and TNF-a levels, while less platelet counts than bone marrow HCMV (--) patients (P〈0.05). Marrow HCMV (+) pa- tients in the CITP group showed higher IL-6 and TNF-a levels and less platelet counts than HCMV (-) patients in the AITP group (P%0.05). No significant difference in average age, IL-6 and TNF-a levels or platelet counts were found between the serum HCMV (+) patients in AITP group and CITP group. Con- clusion. Bone marrow HCMV infection may be one cause of ITP. Bone marrow HCMV infection may ag- gravate children ITP and make it tend to be chronic, probably by affecting immune system to damage for- mation of platelets.
Keywords:Cytomegalovirus  Children  Thrombocytopenic purpura  Infection
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