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儿童及青少年风湿性疾病中的慢性人细小病毒B19感染

Chronic human parvovirus B19 infection in rheumatic disease of childhood and adolescence.

作者信息

Lehmann Hartwig W, Kühner Lucia, Beckenlehner Karin, Müller-Godeffroy Esther, Heide Karl-Günter, Küster Rolf-Michael, Modrow Susanne

机构信息

Department of Paediatric Rheumatology, Rheumaklinik Bad Bramstedt, Postfach 14 48, 24572 Bad Bramstedt, Germany.

出版信息

J Clin Virol. 2002 Aug;25(2):135-43. doi: 10.1016/s1386-6532(01)00247-5.

Abstract

Parvovirus B19 causes erythema infectiosum in children, but the virus is associated with an increasing range of different diseases. About 20% of infections are associated with delayed virus elimination and viremia persisting over several months or years. These persistent B19-infections are characterised by the presence of IgG against the non-structural protein NS1. This study aimed to find further evidence for an association of parvovirus B19 persistence with VP1/2- and NS1-specific IgG-antibodies in children suffering from rheumatic diseases of childhood. Forty-eight children and adolescents with joint complaints lasting longer than 1 year including patients with juvenile systemic sclerosis and juvenile dermatomyositis showed antibodies against the viral NS1-protein. Laboratory markers of inflammation, humoral immune response against parvovirus B19 proteins and the presence of viral genomes in patients' sera as well as in 124 healthy children were investigated. Almost 50% of the patients showed laboratory signs of chronic inflammation. B19-DNA was amplified in 31% of patients' sera and 7% of the controls (P<0.0001). VP2-specific IgM was detectable in 50% of the patients' and 6% of control sera. NS1-specific immune reactions were linked to persistent B19-infection as indicated by the presence of viral genomes in the peripheral blood and of VP2-specific IgM years after disease onset. To estimate the severity of the disease and the clinical course, the number of affected and functionally impaired joints were noted and compared with the records from patients' initial visit in the hospital. Disease related complications were registered. Impairment of activities of daily living was assessed by Childhood Health Assessment Questionnaire (CHAQ)- and Munich Quality of Life Questionnaire (KINDL)-tests. During observation the clinical state of four patients worsened, 27 improved, the others remained stable. Twenty-four children were restricted in their daily activities.

摘要

细小病毒B19可导致儿童传染性红斑,但该病毒与越来越多的不同疾病有关。约20%的感染与病毒清除延迟及病毒血症持续数月或数年有关。这些持续性B19感染的特征是存在针对非结构蛋白NS1的IgG。本研究旨在寻找更多证据,证明儿童风湿性疾病患者中细小病毒B19持续性感染与VP1/2和NS1特异性IgG抗体之间的关联。48名关节不适持续超过1年的儿童和青少年,包括青少年系统性硬化症和青少年皮肌炎患者,显示出针对病毒NS1蛋白的抗体。对炎症的实验室指标、针对细小病毒B19蛋白的体液免疫反应以及患者血清和124名健康儿童血清中病毒基因组的存在情况进行了研究。近50%的患者出现慢性炎症的实验室迹象。31%的患者血清和7%的对照组中扩增出B19-DNA(P<0.0001)。50%的患者血清和6%的对照血清中可检测到VP2特异性IgM。如疾病发作数年外周血中存在病毒基因组及VP2特异性IgM所示,NS1特异性免疫反应与持续性B19感染有关。为评估疾病的严重程度和临床病程,记录了受累关节和功能受损关节的数量,并与患者首次住院记录进行比较。记录了与疾病相关的并发症。通过儿童健康评估问卷(CHAQ)和慕尼黑生活质量问卷(KINDL)测试评估日常生活活动的受损情况。在观察期间,4名患者的临床状态恶化,27名患者改善,其他患者保持稳定。24名儿童的日常活动受到限制。

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