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再生障碍性贫血患者中的人细小病毒B19

Human parvovirus B19 in patients with aplastic anemia.

作者信息

Mishra Baijayantimala, Malhotra Pankaj, Ratho Radha Kanta, Singh Mini P, Varma Subhash, Varma Neelam

机构信息

Department of Virology, Post Graduate Institute of Medical Education & Research, 160012 Chandigarh, India.

出版信息

Am J Hematol. 2005 Jun;79(2):166-7. doi: 10.1002/ajh.20347.

Abstract

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.

摘要

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。

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