Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan.
J Med Virol. 2014 Dec;86(12):2102-6. doi: 10.1002/jmv.23930. Epub 2014 Jun 24.
Several publications concerning the methods of real-time PCR for human parvovirus B19 (B19V) have appeared and some case reports mention B19V DNA loads. However, no large-scale study quantitating levels of B19V DNA in common or representative B19V manifestations such as erythema infectiosum and aplastic crisis has been performed. Consequently, using the TaqMan PCR assay, the B19V load in a large sample of subjects with erythema infectiosum or aplastic crisis was quantitated. Sixty-five subjects in the acute phase of erythema infectiosum were involved, and in addition 22 serum samples from seven subjects with B19V-associated aplastic crisis complicating chronic hemolytic anemia were also analyzed. In the acute phase of erythema infectiosum the median B19V DNA load in the serum samples from the acute phase of erythema infectiosum was 7.63 × 10(5) genomes/ml, (range from 4.48 × 10(3) to 8.31 × 10(6) genomes/ml). The serum B19V DNA load during the acute phase of aplastic crisis complicating chronic hemolytic anemia was extremely high, that is 10(10) -10(13) genomes/ml, and decreased gradually to around 10(5) genomes/ml over 1-2 months. Although all subjects followed an almost uniform and typical clinical course of erythema infectiosum, there was a large individual variation of B19V DNA loads, that is differences of over 1,000 times. Extremely high B19V loads were observed in subjects with aplastic crisis. This study is the first large scale report of studies of the B19V DNA loads in subjects with erythema infectiosum and aplastic crisis, the most common and significant clinical manifestations by B19V infections.
已有多篇关于人细小病毒 B19(B19V)实时 PCR 方法的出版物发表,部分病例报告提到了 B19V DNA 载量。然而,尚未对常见或代表性 B19V 表现形式(如传染性红斑和再生障碍危象)进行定量分析 B19V DNA 水平的大规模研究。因此,我们使用 TaqMan PCR 法对患有传染性红斑或再生障碍危象的大量患者的 B19V 载量进行了定量分析。我们纳入了 65 名处于传染性红斑急性期的患者,另外还分析了 7 名伴有慢性溶血性贫血的 B19V 相关再生障碍危象患者的 22 份血清样本。在传染性红斑急性期,传染性红斑急性期血清样本的中位 B19V DNA 载量为 7.63×10(5) 基因组/ml(范围为 4.48×10(3) 至 8.31×10(6) 基因组/ml)。慢性溶血性贫血合并再生障碍危象急性期血清 B19V DNA 载量极高,即 10(10) 至 10(13) 基因组/ml,并在 1 至 2 个月内逐渐降至约 10(5) 基因组/ml。尽管所有患者均经历了几乎相同的典型传染性红斑临床病程,但 B19V DNA 载量存在较大个体差异,差异超过 1000 倍。再生障碍危象患者的 B19V 载量极高。本研究首次大规模报告了传染性红斑和再生障碍危象患者的 B19V DNA 载量研究,这是 B19V 感染最常见和最重要的临床表现。