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免疫功能正常和免疫功能低下的呼吸道疾病患者中的 Merkel 细胞多瘤病毒 DNA。

Merkel cell polyomavirus DNA in immunocompetent and immunocompromised patients with respiratory disease.

机构信息

Department of Virology, University of Manchester, Manchester, UK.

出版信息

J Med Virol. 2011 Dec;83(12):2220-4. doi: 10.1002/jmv.22222.

Abstract

Merkel cell polyomavirus (MCPyV) was identified originally in association with a rare but aggressive skin cancer, Merkel cell carcinoma. The virus has since been found in the respiratory tract of some patients with respiratory disease. However, the role of MCPyV in the causation of respiratory disease has not been established. To determine the prevalence of MCPyV in 305 respiratory samples from immunocompetent and immunocompromised patients and evaluate their contribution to respiratory diseases, specimens were screened for MCPyV using single, multiplex, or real-time PCR; co-infection with other viruses was examined. Of the 305 samples tested, 10 (3.27%) were positive for MCPyV. The virus was found in two groups of patients: in 6 (2%) nasopharyngeal aspirate samples from children aged 26 days to 7 months who were immunocompetent; and in 4 (1.3%) of nasopharyngeal aspirate samples taken from patients aged 41 to 69 years who were severely immunosuppressed from leukemia or transplant therapy. Both groups had upper or lower respiratory tract infection. Co-infections with other viruses were found in 30% of the MCPyV positive samples. The data present a pattern of infection similar to that seen with the polyomaviruses JC and BK in which the virus is acquired during childhood, probably by the respiratory route. The viruses then establish latency and become reactivated in the event of immunosuppression.

摘要

默克尔细胞多瘤病毒(MCPyV)最初是在一种罕见但侵袭性很强的皮肤癌——默克尔细胞癌中发现的。此后,在一些患有呼吸道疾病的患者的呼吸道中发现了这种病毒。然而,MCPyV 在引起呼吸道疾病中的作用尚未确定。为了确定 305 份来自免疫功能正常和免疫功能低下患者的呼吸道样本中 MCPyV 的流行情况,并评估其对呼吸道疾病的贡献,使用单重、多重或实时 PCR 对标本进行了 MCPyV 筛查;同时还检查了与其他病毒的合并感染情况。在 305 个测试样本中,有 10 个(3.27%)样本对 MCPyV 呈阳性。该病毒存在于两组患者中:一组为 26 天大至 7 个月大的免疫功能正常的儿童的 6 份(2%)鼻咽抽吸物样本;另一组为 4 份(1.3%)来自白血病或移植治疗导致严重免疫抑制的 41 至 69 岁患者的鼻咽抽吸物样本。两组患者均有上呼吸道或下呼吸道感染。在 30%的 MCPyV 阳性样本中发现了与 JC 和 BK 多瘤病毒相似的合并感染模式。在这些病毒中,病毒在儿童时期通过呼吸道获得,可能是通过呼吸道获得的。然后,这些病毒建立潜伏状态,并在发生免疫抑制时重新激活。

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