儿童特发性血小板减少性紫癜:与人细小病毒B19感染有关。

J C Murray, P K Kelley, W R Hogrefe, K L McClain
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引用次数: 0

摘要

目的:人细小病毒B19感染是慢性溶血性贫血患者一过性再生危象的最常见原因。多例同时发生B19感染和血小板减少症的儿童报告,以及已知的实验性B19感染和血小板减少症之间的关联,促使我们假设B19可能与儿童特发性或免疫性血小板减少性紫癜(ITP)有关。由于缺乏关于ITP的病毒病因的证据,我们进行了一项全面的研究,以探索其与B19感染的可能关系。患者和方法:对35例既往健康的ITP患儿进行前瞻性研究。采用聚合酶链反应(PCR)检测骨髓和外周血B19 DNA。采用基于B19 VP1抗原的酶联免疫吸附法检测血清中抗B19免疫球蛋白(Ig) M和IgG抗体。14名健康儿童作为对照组进行外周血PCR和血清学分析。结果:研究人群的临床和实验室表现为典型的ITP。35例患者中有17例(49%)外周血、骨髓或两者均有B19 DNA。35例患者中有6例(17%)有抗b19 IgM抗体。35例患者中8例(23%)血清抗b19 IgG阳性。对照组无PCR阳性和抗b19 IgM标本。结论:我们的研究结果提示,感染人细小病毒B19可能与儿童ITP有关。PCR方法学和血清学检测方法在确定B19与ITP相关的病理生物学方面的作用有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Childhood idiopathic thrombocytopenic purpura: association with human parvovirus B19 infection.

Purpose: Infection with human parvovirus B19 is the most common cause of transient aplastic crisis in patients with chronic hemolytic anemia. Multiple reports of children with simultaneous B19 infection and thrombocytopenia as well as the known association between experimental B19 infection and thrombocytopenia prompted us to hypothesize that B19 may be associated with childhood idiopathic, or immune, thrombocytopenic purpura (ITP). Because there is a paucity of evidence regarding a viral etiology for ITP, we performed a comprehensive study to explore its possible relationship to B19 infection.

Patients and methods: Thirty-five previously healthy children with ITP were studied prospectively. Bone marrow and peripheral blood were analyzed for B19 DNA using the polymerase chain reaction (PCR). Serum was analyzed for anti-B19 immunoglobulin (Ig) M and IgG antibodies using a B19 VP1 antigen-based enzyme-linked immunosorbent assay. Fourteen healthy children served as controls for peripheral blood PCR and serologic analyses.

Results: The presenting clinical and laboratory features of the study population were typical of classic ITP. Seventeen of the 35 patients (49%) had evidence of B19 DNA in the peripheral blood, bone marrow, or both. Six of 35 (17%) had anti-B19 IgM antibodies. Eight of 35 (23%) were anti-B19 IgG seropositive. The control group had no positive PCR or anti-B19 IgM specimens.

Conclusions: Our results suggest that infection with human parvovirus B19 may be associated with childhood ITP. More investigation is warranted regarding the role of PCR methodology and serologic detection methods in defining B19 pathobiology as it relates to ITP.

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