Localization of parvovirus B19 in the renal allografts of healthy donors.

IF 3.1 3区 医学 Q1 PATHOLOGY
Dan Inoue, Takashi Oda, Tadaki Suzuki, Michiyo Kataoka, Sachiko Iwama, Yuko Dohi, Osamu Konno, Muneharu Yamada, Hironori Takeuchi, Hitoshi Iwamoto
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引用次数: 0

Abstract

Parvovirus B19 (PVB19) is usually not a subject of pre-transplant evaluation. Little is known regarding the localization of PVB19 in normal kidneys, particularly in relation to its cellular receptor, the P antigen. Tissue specimens obtained from 0-h renal allograft biopsies were investigated for the presence of PVB19 DNA by polymerase chain reaction (PCR) and the relative localization of P antigen and PVB19-related protein by double immunofluorescence staining. Double staining of in situ hybridization for PVB19 DNA and immunofluorescence staining for PVB19-related proteins was also performed. The presence of the virus was further evaluated by electron microscopy in selected biopsy specimens. PCR analysis detected PVB19 DNA in 39 out of 112 (35%) tissue samples. Immunohistochemical analysis of these 39 PVB19 DNA-positive samples revealed that 28 (72%) exhibited positive staining for PVB19-related proteins within some tubular epithelial cells. Electron microscopy demonstrated regular polygonal virus-like particles within tubular epithelial cells. Furthermore, most PVB19-positive tubular epithelial cells expressed the P antigen on their apical surfaces. PVB19 DNA and PVB19-related proteins co-localized in some tubular epithelial cells. Thus, approximately 1/3 of healthy adult kidneys contain PVB19, which is localized mainly in distal tubules expressing P antigens on their apical surface. The concurrent detection of PVB19 DNA and proteins, along with the visualization of virus-like particles by electron microscopy, suggests that PVB19 could live with protein-producing capacity. Given the relatively high frequency of detection, the possibility of PVB19 infection should be carefully considered in the context of kidney transplantation.

细小病毒B19在健康供体移植肾中的定位。
细小病毒B19 (PVB19)通常不是移植前评估的对象。关于PVB19在正常肾脏中的定位,特别是其细胞受体P抗原的定位,我们所知甚少。采用聚合酶链反应(PCR)检测移植肾0 h组织标本PVB19 DNA的存在,双免疫荧光染色检测P抗原和PVB19相关蛋白的相对定位。PVB19 DNA原位杂交双染色和PVB19相关蛋白免疫荧光染色。在选定的活检标本中,通过电子显微镜进一步评估病毒的存在。PCR分析在112个组织样本中的39个(35%)中检测到PVB19 DNA。39例PVB19 dna阳性样本的免疫组化分析显示,28例(72%)在一些小管上皮细胞中显示PVB19相关蛋白阳性。电镜显示小管上皮细胞内有规则的多角形病毒样颗粒。大多数pvb19阳性的小管上皮细胞在其顶端表面表达P抗原。PVB19 DNA和PVB19相关蛋白在一些小管上皮细胞中共定位。因此,大约1/3的健康成人肾脏含有PVB19, PVB19主要位于远端小管,在其顶端表面表达P抗原。PVB19 DNA和蛋白质的同时检测,以及电子显微镜下病毒样颗粒的可视化,表明PVB19具有生产蛋白质的能力。鉴于PVB19的检测频率相对较高,在肾移植的背景下,应仔细考虑PVB19感染的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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