Mishra Baijayantimala, Malhotra Pankaj, Ratho Radha Kanta, Singh Mini P, Varma Subhash, Varma Neelam
Department of Virology, Post Graduate Institute of Medical Education & Research, 160012 Chandigarh, India.
Am J Hematol. 2005 Jun;79(2):166-7. doi: 10.1002/ajh.20347.
Aplastic anemia is characterized by pancytopenia with hypoplastic bone marrow. Various factors including viral infections have been implicated as the precipitating factors. Human parvovirus B19 has been associated with red-cell aplasia, leukopenia, and thrombocytopenia. The present study was carried out to determine the role of parvovirus B19 in aplastic anemia patients. Twenty-seven aplastic anemia patients and 20 healthy controls were tested for the presence of parvovirus B19 infection by detecting parvovirus B19-specific IgM by ELISA and viral DNA by PCR. Parvovirus B19 IgM and viral DNA were detected in significantly higher numbers of patients in comparison to the controls (40.7% vs. 5%, P < 0.01; 37% vs. 0%, P < 0.001, respectively). The presence of parvovirus DNA in aplastic anemia patients indicates active or recent infection. However, more studies are needed to explore the mechanism of bone-marrow aplasia due to human parvovirus B19 infection.
再生障碍性贫血的特征是全血细胞减少伴骨髓造血功能低下。包括病毒感染在内的多种因素被认为是诱发因素。人类细小病毒B19与红细胞再生障碍、白细胞减少和血小板减少有关。本研究旨在确定细小病毒B19在再生障碍性贫血患者中的作用。通过ELISA检测细小病毒B19特异性IgM以及通过PCR检测病毒DNA,对27例再生障碍性贫血患者和20名健康对照进行了细小病毒B19感染检测。与对照组相比,再生障碍性贫血患者中检测到细小病毒B19 IgM和病毒DNA的人数明显更多(分别为40.7%对5%,P<0.01;37%对0%,P<0.001)。再生障碍性贫血患者中细小病毒DNA的存在表明有活跃或近期感染。然而,需要更多的研究来探索人类细小病毒B19感染导致骨髓再生障碍的机制。