Obeid Obeid E
Department of Microbiology, College of Medicine, University of Dammam, Saudi Arabia.
J Infect Dev Ctries. 2011 Jul 27;5(7):535-9. doi: 10.3855/jidc.1807.
Parvovirus B19 is a cause of hemolysis and red blood cell aplasia in patients with sickle cell anemia. The present study aimed to assess parvovirus B19 infection among sickle cell anemia patients.
All patients (n = 138) included in the study were sickle cell anemia patients. Blood donors were used as a control group. Assessment of parvovirus B19 antibodies and viral DNA was performed using established methods of detection and B19 recomBlot assay.
Detectable levels of parvovirus B19 IgG were found in 52 samples (37.6%) whereas anti-parvovirus B19 IgM antibodies were detected in four (2.89 %) patients of the sickle-cell anemia group. Anti-B19 IgM-positive samples contained B19-viral DNA. These four patients presented with fever, malaise, pallor and no cutaneous rash. Anti-parvovirus B19 antibodies were detected in 22 (39.3%) of the control blood donors group. Anti-parvovirus B19 IgM antibodies were not detected in the control group. Using the recomBlot assay, 58 test samples (42%) were found to contain detectable levels of Parvovirus B19 antibodies. All the samples that were positive for parvovirus B19 IgG by the ELISA were also positive by the recomBlot assay. Six samples were only positive by the recomBlot assay and not by the ELISA. Two of these six samples were positive for B19 viral DNA.
Establishing the extent of parvovirus B19 infection in sickle cell anemia patients will help in proper management of aplastic crisis in such patients. The B19 recomBlot assay may be suitable as a confirmatory assay.
细小病毒B19是镰状细胞贫血患者发生溶血和红细胞再生障碍的一个病因。本研究旨在评估镰状细胞贫血患者中的细小病毒B19感染情况。
本研究纳入的所有患者(n = 138)均为镰状细胞贫血患者。献血者作为对照组。采用既定的检测方法和B19重组印迹法对细小病毒B19抗体和病毒DNA进行评估。
在52份样本(37.6%)中检测到可检测水平的细小病毒B19 IgG,而在镰状细胞贫血组的4名患者(2.89%)中检测到抗细小病毒B19 IgM抗体。抗B19 IgM阳性样本含有B19病毒DNA。这4名患者表现为发热、不适、面色苍白且无皮疹。在对照组献血者中,22名(39.3%)检测到抗细小病毒B19抗体。对照组未检测到抗细小病毒B19 IgM抗体。使用重组印迹法,发现58个测试样本(42%)含有可检测水平的细小病毒B19抗体。通过酶联免疫吸附测定法检测细小病毒B19 IgG呈阳性的所有样本,通过重组印迹法检测也呈阳性。6个样本仅通过重组印迹法呈阳性,而酶联免疫吸附测定法呈阴性。这6个样本中有2个B19病毒DNA呈阳性。
确定镰状细胞贫血患者中细小病毒B19感染的程度将有助于对此类患者再生障碍危象进行适当管理。B19重组印迹法可能适合作为一种确证检测方法。