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系统性硬化症皮肤中人类细小病毒B19 DNA的患病率增加。

Increased prevalence of human parvovirus B19 DNA in systemic sclerosis skin.

作者信息

Ohtsuka T, Yamazaki S

机构信息

Department of Dermatology, Dokkyo Koshigaya Hospital, 2-1-50, Saitoma, 343-8555, Japan.

出版信息

Br J Dermatol. 2004 Jun;150(6):1091-5. doi: 10.1111/j.0007-0963.2004.05930.x.

DOI:10.1111/j.0007-0963.2004.05930.x
PMID:15214893
Abstract

BACKGROUND

Human parvovirus B19 is a small, single-stranded DNA virus encoding two structural capsid proteins and a nonstructural protein. It is the aetiological agent of erythema infectiosum and transient aplastic crisis in patients with haemolytic anaemia, and has been associated with fetal death, arthritis and chronic anaemia. In recent years, the possible involvement of parvovirus B19 in systemic sclerosis (SSc) has been reported.

OBJECTIVES

To determine whether human parvovirus B19 DNA can be detected in SSc skin tissue specimens.

METHODS

Normal subjects (n = 97) and patients with SSc (n = 48), systemic lupus erythematosus (n = 16), dermatomyositis (n = 8), morphoea (n = 6) and graft-versus-host disease (n = 8) were studied. Crude DNA was extracted from skin tissue specimens. We attempted to determine whether human parvovirus B19 could be detected in the skin of SSc using nested polymerase chain reaction (PCR). PCR amplification was performed with specifically designed first and second primer pairs for parvovirus B19 DNA.

RESULTS

After the first PCR, the occurrence rate of parvovirus B19 DNA in SSc skin tissues (36 of 48, 75%) was significantly elevated in comparison with that in normal controls (50 of 97, 52%) (P < 0.01). After the second PCR, the occurrence rate of parvovirus B19 DNA in SSc skin tissues (36 of 48, 75%) was significantly elevated compared with that in normal controls (53 of 97, 55%) (P < 0.02). The occurrence rates in the other diseases showed no significant difference from that in normal controls.

CONCLUSIONS

The increased prevalence of human parvovirus B19 DNA in SSc skin showed the possibility that the virus may be involved in the formation of skin tissue abnormalities in the disease.

摘要

背景

人细小病毒B19是一种小型单链DNA病毒,编码两种结构衣壳蛋白和一种非结构蛋白。它是传染性红斑和溶血性贫血患者短暂再生障碍危象的病原体,并且与胎儿死亡、关节炎和慢性贫血有关。近年来,已有报道细小病毒B19可能与系统性硬化症(SSc)有关。

目的

确定在SSc皮肤组织标本中是否能检测到人细小病毒B19 DNA。

方法

研究了正常受试者(n = 97)和患有SSc(n = 48)、系统性红斑狼疮(n = 16)、皮肌炎(n = 8)、硬斑病(n = 6)和移植物抗宿主病(n = 8)的患者。从皮肤组织标本中提取粗DNA。我们试图使用巢式聚合酶链反应(PCR)确定在SSc皮肤中是否能检测到人细小病毒B19。使用针对细小病毒B19 DNA专门设计的第一对和第二对引物进行PCR扩增。

结果

第一次PCR后,SSc皮肤组织中细小病毒B19 DNA的发生率(48例中的36例,75%)与正常对照组(97例中的50例,52%)相比显著升高(P < 0.01)。第二次PCR后,SSc皮肤组织中细小病毒B19 DNA的发生率(48例中的36例,75%)与正常对照组(97例中的53例,55%)相比显著升高(P < 0.02)。其他疾病中的发生率与正常对照组无显著差异。

结论

SSc皮肤中人细小病毒B19 DNA患病率的增加表明该病毒可能参与了该疾病皮肤组织异常形成的可能性。

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