Loading…
BK polyomavirus infection: more than 50 years and still a threat to kidney transplant recipients
BK polyomavirus (BKPyV) is a ubiquitous human polyomavirus and a major infection after kidney transplantation, primarily due to immunosuppression. BKPyV reactivation can manifest as viruria in 30%-40%, viremia in 10%-20%, and BK polyomavirus-associated nephropathy (BKPyVAN) in 1%-10% of recipients....
Saved in:
Published in: | Frontiers in transplantation 2024, Vol.3, p.1309927 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c2657-7b7e2ef185fe5daa6c939e02892464bb61aa963e8e6aa0249b5c9ed8f6f031dc3 |
container_end_page | |
container_issue | |
container_start_page | 1309927 |
container_title | Frontiers in transplantation |
container_volume | 3 |
creator | Parajuli, Sandesh Aziz, Fahad Zhong, Weixiong Djamali, Arjang |
description | BK polyomavirus (BKPyV) is a ubiquitous human polyomavirus and a major infection after kidney transplantation, primarily due to immunosuppression. BKPyV reactivation can manifest as viruria in 30%-40%, viremia in 10%-20%, and BK polyomavirus-associated nephropathy (BKPyVAN) in 1%-10% of recipients. BKPyVAN is an important cause of kidney graft failure. Although the first case of BKPyV was identified in 1971, progress in its management has been limited. Specifically, there is no safe and effective antiviral agent or vaccine to treat or prevent the infection. Even in the current era, the mainstay approach to BKPyV is a reduction in immunosuppression, which is also limited by safety (risk of
donor specific antibody and rejection) and efficacy (graft failure). However, recently BKPyV has been getting more attention in the field, and some new treatment strategies including the utilization of viral-specific T-cell therapy are emerging. Given all these challenges, the primary focus of this article is complications associated with BKPyV, as well as strategies to mitigate negative outcomes. |
doi_str_mv | 10.3389/frtra.2024.1309927 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_20a8dc62c0f24302bcab42123f22eb0f</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_20a8dc62c0f24302bcab42123f22eb0f</doaj_id><sourcerecordid>3079172942</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2657-7b7e2ef185fe5daa6c939e02892464bb61aa963e8e6aa0249b5c9ed8f6f031dc3</originalsourceid><addsrcrecordid>eNpVkU1P3DAQhqOqqCDgD_RQ-djLLvY4ceJeqha1gIrUS3t2J84YTJM4tb1I--9r2AXBaaz5eOYdv1X1XvC1lJ0-czFHXAOHei0k1xraN9URdEKuoK752xfvw-o0pTvOOXStahv1rjosAC1bVR9Vf77-YEsYt2HCex83ifnZkc0-zJ_YFCKxfIszazjbEsbEcB5Yyn4cGZZKJMwsB_bXDzNtWRE0p2XEObNI1i-e5pxOqgOHY6LTfTyufn__9uv8cnX98-Lq_Mv1yoJq2lXbtwTkRNc4agZEZbXUVCRrqFXd90ogaiWpI4VYjtZ9YzUNnVOOSzFYeVxd7bhDwDuzRD9h3JqA3jwmQrwxGLO3Ixng2A1WgeUOasmht9jXIEA6AOq5K6zPO9ay6ScabLkj4vgK-roy-1tzE-6NKJBGclEIH_eEGP5tKGUz-WRpLJ9DYZOM5K0WLegaSivsWm0MKUVyz3sENw9Wm0erzYPVZm91GfrwUuHzyJOx8j9fsadR</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3079172942</pqid></control><display><type>article</type><title>BK polyomavirus infection: more than 50 years and still a threat to kidney transplant recipients</title><source>PubMed Central</source><creator>Parajuli, Sandesh ; Aziz, Fahad ; Zhong, Weixiong ; Djamali, Arjang</creator><creatorcontrib>Parajuli, Sandesh ; Aziz, Fahad ; Zhong, Weixiong ; Djamali, Arjang</creatorcontrib><description>BK polyomavirus (BKPyV) is a ubiquitous human polyomavirus and a major infection after kidney transplantation, primarily due to immunosuppression. BKPyV reactivation can manifest as viruria in 30%-40%, viremia in 10%-20%, and BK polyomavirus-associated nephropathy (BKPyVAN) in 1%-10% of recipients. BKPyVAN is an important cause of kidney graft failure. Although the first case of BKPyV was identified in 1971, progress in its management has been limited. Specifically, there is no safe and effective antiviral agent or vaccine to treat or prevent the infection. Even in the current era, the mainstay approach to BKPyV is a reduction in immunosuppression, which is also limited by safety (risk of
donor specific antibody and rejection) and efficacy (graft failure). However, recently BKPyV has been getting more attention in the field, and some new treatment strategies including the utilization of viral-specific T-cell therapy are emerging. Given all these challenges, the primary focus of this article is complications associated with BKPyV, as well as strategies to mitigate negative outcomes.</description><identifier>ISSN: 2813-2440</identifier><identifier>EISSN: 2813-2440</identifier><identifier>DOI: 10.3389/frtra.2024.1309927</identifier><identifier>PMID: 38993764</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>acute kidney injury (AKI) ; antibody-mediated rejection (AMR) ; BK polyomavirus (BKPyV) ; BKPyV management ; BKPyV-associated nephropathy (BKPyVAN) ; Transplantation</subject><ispartof>Frontiers in transplantation, 2024, Vol.3, p.1309927</ispartof><rights>2024 Parajuli, Aziz, Zhong and Djamali.</rights><rights>2024 Parajuli, Aziz, Zhong and Djamali. 2024 Parajuli, Aziz, Zhong and Djamali</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2657-7b7e2ef185fe5daa6c939e02892464bb61aa963e8e6aa0249b5c9ed8f6f031dc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11235301/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11235301/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,4024,27923,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38993764$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Parajuli, Sandesh</creatorcontrib><creatorcontrib>Aziz, Fahad</creatorcontrib><creatorcontrib>Zhong, Weixiong</creatorcontrib><creatorcontrib>Djamali, Arjang</creatorcontrib><title>BK polyomavirus infection: more than 50 years and still a threat to kidney transplant recipients</title><title>Frontiers in transplantation</title><addtitle>Front Transplant</addtitle><description>BK polyomavirus (BKPyV) is a ubiquitous human polyomavirus and a major infection after kidney transplantation, primarily due to immunosuppression. BKPyV reactivation can manifest as viruria in 30%-40%, viremia in 10%-20%, and BK polyomavirus-associated nephropathy (BKPyVAN) in 1%-10% of recipients. BKPyVAN is an important cause of kidney graft failure. Although the first case of BKPyV was identified in 1971, progress in its management has been limited. Specifically, there is no safe and effective antiviral agent or vaccine to treat or prevent the infection. Even in the current era, the mainstay approach to BKPyV is a reduction in immunosuppression, which is also limited by safety (risk of
donor specific antibody and rejection) and efficacy (graft failure). However, recently BKPyV has been getting more attention in the field, and some new treatment strategies including the utilization of viral-specific T-cell therapy are emerging. Given all these challenges, the primary focus of this article is complications associated with BKPyV, as well as strategies to mitigate negative outcomes.</description><subject>acute kidney injury (AKI)</subject><subject>antibody-mediated rejection (AMR)</subject><subject>BK polyomavirus (BKPyV)</subject><subject>BKPyV management</subject><subject>BKPyV-associated nephropathy (BKPyVAN)</subject><subject>Transplantation</subject><issn>2813-2440</issn><issn>2813-2440</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkU1P3DAQhqOqqCDgD_RQ-djLLvY4ceJeqha1gIrUS3t2J84YTJM4tb1I--9r2AXBaaz5eOYdv1X1XvC1lJ0-czFHXAOHei0k1xraN9URdEKuoK752xfvw-o0pTvOOXStahv1rjosAC1bVR9Vf77-YEsYt2HCex83ifnZkc0-zJ_YFCKxfIszazjbEsbEcB5Yyn4cGZZKJMwsB_bXDzNtWRE0p2XEObNI1i-e5pxOqgOHY6LTfTyufn__9uv8cnX98-Lq_Mv1yoJq2lXbtwTkRNc4agZEZbXUVCRrqFXd90ogaiWpI4VYjtZ9YzUNnVOOSzFYeVxd7bhDwDuzRD9h3JqA3jwmQrwxGLO3Ixng2A1WgeUOasmht9jXIEA6AOq5K6zPO9ay6ScabLkj4vgK-roy-1tzE-6NKJBGclEIH_eEGP5tKGUz-WRpLJ9DYZOM5K0WLegaSivsWm0MKUVyz3sENw9Wm0erzYPVZm91GfrwUuHzyJOx8j9fsadR</recordid><startdate>2024</startdate><enddate>2024</enddate><creator>Parajuli, Sandesh</creator><creator>Aziz, Fahad</creator><creator>Zhong, Weixiong</creator><creator>Djamali, Arjang</creator><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>2024</creationdate><title>BK polyomavirus infection: more than 50 years and still a threat to kidney transplant recipients</title><author>Parajuli, Sandesh ; Aziz, Fahad ; Zhong, Weixiong ; Djamali, Arjang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2657-7b7e2ef185fe5daa6c939e02892464bb61aa963e8e6aa0249b5c9ed8f6f031dc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>acute kidney injury (AKI)</topic><topic>antibody-mediated rejection (AMR)</topic><topic>BK polyomavirus (BKPyV)</topic><topic>BKPyV management</topic><topic>BKPyV-associated nephropathy (BKPyVAN)</topic><topic>Transplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Parajuli, Sandesh</creatorcontrib><creatorcontrib>Aziz, Fahad</creatorcontrib><creatorcontrib>Zhong, Weixiong</creatorcontrib><creatorcontrib>Djamali, Arjang</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Parajuli, Sandesh</au><au>Aziz, Fahad</au><au>Zhong, Weixiong</au><au>Djamali, Arjang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>BK polyomavirus infection: more than 50 years and still a threat to kidney transplant recipients</atitle><jtitle>Frontiers in transplantation</jtitle><addtitle>Front Transplant</addtitle><date>2024</date><risdate>2024</risdate><volume>3</volume><spage>1309927</spage><pages>1309927-</pages><issn>2813-2440</issn><eissn>2813-2440</eissn><abstract>BK polyomavirus (BKPyV) is a ubiquitous human polyomavirus and a major infection after kidney transplantation, primarily due to immunosuppression. BKPyV reactivation can manifest as viruria in 30%-40%, viremia in 10%-20%, and BK polyomavirus-associated nephropathy (BKPyVAN) in 1%-10% of recipients. BKPyVAN is an important cause of kidney graft failure. Although the first case of BKPyV was identified in 1971, progress in its management has been limited. Specifically, there is no safe and effective antiviral agent or vaccine to treat or prevent the infection. Even in the current era, the mainstay approach to BKPyV is a reduction in immunosuppression, which is also limited by safety (risk of
donor specific antibody and rejection) and efficacy (graft failure). However, recently BKPyV has been getting more attention in the field, and some new treatment strategies including the utilization of viral-specific T-cell therapy are emerging. Given all these challenges, the primary focus of this article is complications associated with BKPyV, as well as strategies to mitigate negative outcomes.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>38993764</pmid><doi>10.3389/frtra.2024.1309927</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2813-2440 |
ispartof | Frontiers in transplantation, 2024, Vol.3, p.1309927 |
issn | 2813-2440 2813-2440 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_20a8dc62c0f24302bcab42123f22eb0f |
source | PubMed Central |
subjects | acute kidney injury (AKI) antibody-mediated rejection (AMR) BK polyomavirus (BKPyV) BKPyV management BKPyV-associated nephropathy (BKPyVAN) Transplantation |
title | BK polyomavirus infection: more than 50 years and still a threat to kidney transplant recipients |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T02%3A06%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=BK%20polyomavirus%20infection:%20more%20than%2050%20years%20and%20still%20a%20threat%20to%20kidney%20transplant%20recipients&rft.jtitle=Frontiers%20in%20transplantation&rft.au=Parajuli,%20Sandesh&rft.date=2024&rft.volume=3&rft.spage=1309927&rft.pages=1309927-&rft.issn=2813-2440&rft.eissn=2813-2440&rft_id=info:doi/10.3389/frtra.2024.1309927&rft_dat=%3Cproquest_doaj_%3E3079172942%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c2657-7b7e2ef185fe5daa6c939e02892464bb61aa963e8e6aa0249b5c9ed8f6f031dc3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3079172942&rft_id=info:pmid/38993764&rfr_iscdi=true |