Evidence map›Paper›PMID 40783628›Full record

ArticleVirchows Archiv : an international journal of pathology2025

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

Dan Inoue, Takashi Oda, Tadaki Suzuki, Michiyo Kataoka, Sachiko Iwama, Yuko Dohi, Osamu Konno, Muneharu Yamada, Hironori Takeuchi, Hitoshi Iwamoto

Erratum issuedAbstract read
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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Dan InoueDepartment of Nephrology and Blood Purification, Kidney Disease Center, Tokyo Medical University Hachioji Medical Center, Hachioji, Tokyo, Japan.
Takashi OdaDepartment of Nephrology and Blood Purification, Kidney Disease Center, Tokyo Medical University Hachioji Medical Center, Hachioji, Tokyo, Japan. takashio@tokyo-med.ac.jp.ORCID http://orcid.org/0000-0002-4134-8535
Tadaki SuzukiDepartment of Pathology, National Institute of Infectious Diseases, Shinjuku-Ku, Tokyo, Japan.ORCID http://orcid.org/0000-0002-3820-9542
Michiyo KataokaDepartment of Pathology, National Institute of Infectious Diseases, Shinjuku-Ku, Tokyo, Japan.ORCID http://orcid.org/0000-0002-2654-8803
Sachiko IwamaDepartment of Nephrology and Blood Purification, Kidney Disease Center, Tokyo Medical University Hachioji Medical Center, Hachioji, Tokyo, Japan.ORCID http://orcid.org/0000-0002-3326-2010
Yuko DohiDepartment of Practical Pharmacy, Tokyo University of Pharmacy and Life Sciences, Hachioji, Tokyo, Japan.
Osamu KonnoDepartment of Kidney Transplantation Surgery, Kidney Disease Center, Tokyo Medical University Hachioji Medical Center, Hachioji, Tokyo, Japan.ORCID http://orcid.org/0000-0001-7706-0616
Muneharu YamadaDepartment of Nephrology and Blood Purification, Kidney Disease Center, Tokyo Medical University Hachioji Medical Center, Hachioji, Tokyo, Japan.ORCID http://orcid.org/0000-0003-0483-0012
Hironori TakeuchiDepartment of Practical Pharmacy, Tokyo University of Pharmacy and Life Sciences, Hachioji, Tokyo, Japan.ORCID http://orcid.org/0000-0002-0954-6988
Hitoshi IwamotoDepartment of Kidney Transplantation Surgery, Kidney Disease Center, Tokyo Medical University Hachioji Medical Center, Hachioji, Tokyo, Japan.

Funding

AMED JP23fk0108637Japan Society for the Promotion of Science London 21K08604
6 · The paper itself

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.

Indexed as

0-h biopsyElectron microscopyKidney transplantationP antigenParvovirus B19Polymerase chain reaction

Identifiers

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.