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Usefulness of BK virus-specific interferon-γ enzyme-linked immunospot assay for predicting the outcome of BK virus infection in kidney transplant recipients

BACKGROUND/AIMS: To investigate if BK virus (BKV)-specific T cell immunity measured by an interferon-γ enzyme-linked immunospot (ELISPOT) assay can predict the outcome of BK virus infection in kidney transplant recipients (KTRs). METHODS: We included 68 KTRs with different viremia status (no viremia...

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Autores principales: Bae, Hyunjoo, Na, Do Hyun, Chang, Ji-Yeun, Park, Ki Hyun, Min, Ji Won, Ko, Eun Jeong, Lee, Hyeyoung, Yang, Chul Woo, Chung, Byung Ha, Oh, Eun-Jee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Internal Medicine 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820663/
https://www.ncbi.nlm.nih.gov/pubmed/32241081
http://dx.doi.org/10.3904/kjim.2019.339
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author Bae, Hyunjoo
Na, Do Hyun
Chang, Ji-Yeun
Park, Ki Hyun
Min, Ji Won
Ko, Eun Jeong
Lee, Hyeyoung
Yang, Chul Woo
Chung, Byung Ha
Oh, Eun-Jee
author_facet Bae, Hyunjoo
Na, Do Hyun
Chang, Ji-Yeun
Park, Ki Hyun
Min, Ji Won
Ko, Eun Jeong
Lee, Hyeyoung
Yang, Chul Woo
Chung, Byung Ha
Oh, Eun-Jee
author_sort Bae, Hyunjoo
collection PubMed
description BACKGROUND/AIMS: To investigate if BK virus (BKV)-specific T cell immunity measured by an interferon-γ enzyme-linked immunospot (ELISPOT) assay can predict the outcome of BK virus infection in kidney transplant recipients (KTRs). METHODS: We included 68 KTRs with different viremia status (no viremia [n = 17], BK viremia [n = 27], and cleared viremia [n = 24]) and 44 healthy controls (HCs). The BK viremia group was divided into controller (< 3 months) and noncontroller (> 3 months) according to sustained duration of BKV infection. We compared BKV-ELISPOT results against five BKV peptides (large tumor antigen [LT], St, VP1-3). RESULTS: BKV-ELISPOT results were higher in three KTRs groups with different BKV infection status than the HCs group (p < 0.05). In KTR groups, they were higher in cleared viremia group than no viremia or BK viremia group. Within the BK viremia group, controller group had higher LT-ELISPOT results compared to noncontroller group (p = 0.032). Also, KTRs without BK virus-associated nephropathy (BKVN) had higher LT, St, VP1, and VP2-ELISPOT results than those with BKVN (p < 0.05). CONCLUSIONS: BKV-ELISPOT assay may be effective in predicting clinical outcomes of BKV infection in terms of clearance of BK virus and development of BKVN.
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spelling pubmed-78206632021-01-27 Usefulness of BK virus-specific interferon-γ enzyme-linked immunospot assay for predicting the outcome of BK virus infection in kidney transplant recipients Bae, Hyunjoo Na, Do Hyun Chang, Ji-Yeun Park, Ki Hyun Min, Ji Won Ko, Eun Jeong Lee, Hyeyoung Yang, Chul Woo Chung, Byung Ha Oh, Eun-Jee Korean J Intern Med Original Article BACKGROUND/AIMS: To investigate if BK virus (BKV)-specific T cell immunity measured by an interferon-γ enzyme-linked immunospot (ELISPOT) assay can predict the outcome of BK virus infection in kidney transplant recipients (KTRs). METHODS: We included 68 KTRs with different viremia status (no viremia [n = 17], BK viremia [n = 27], and cleared viremia [n = 24]) and 44 healthy controls (HCs). The BK viremia group was divided into controller (< 3 months) and noncontroller (> 3 months) according to sustained duration of BKV infection. We compared BKV-ELISPOT results against five BKV peptides (large tumor antigen [LT], St, VP1-3). RESULTS: BKV-ELISPOT results were higher in three KTRs groups with different BKV infection status than the HCs group (p < 0.05). In KTR groups, they were higher in cleared viremia group than no viremia or BK viremia group. Within the BK viremia group, controller group had higher LT-ELISPOT results compared to noncontroller group (p = 0.032). Also, KTRs without BK virus-associated nephropathy (BKVN) had higher LT, St, VP1, and VP2-ELISPOT results than those with BKVN (p < 0.05). CONCLUSIONS: BKV-ELISPOT assay may be effective in predicting clinical outcomes of BKV infection in terms of clearance of BK virus and development of BKVN. The Korean Association of Internal Medicine 2021-01 2020-04-03 /pmc/articles/PMC7820663/ /pubmed/32241081 http://dx.doi.org/10.3904/kjim.2019.339 Text en Copyright © 2021 The Korean Association of Internal Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Bae, Hyunjoo
Na, Do Hyun
Chang, Ji-Yeun
Park, Ki Hyun
Min, Ji Won
Ko, Eun Jeong
Lee, Hyeyoung
Yang, Chul Woo
Chung, Byung Ha
Oh, Eun-Jee
Usefulness of BK virus-specific interferon-γ enzyme-linked immunospot assay for predicting the outcome of BK virus infection in kidney transplant recipients
title Usefulness of BK virus-specific interferon-γ enzyme-linked immunospot assay for predicting the outcome of BK virus infection in kidney transplant recipients
title_full Usefulness of BK virus-specific interferon-γ enzyme-linked immunospot assay for predicting the outcome of BK virus infection in kidney transplant recipients
title_fullStr Usefulness of BK virus-specific interferon-γ enzyme-linked immunospot assay for predicting the outcome of BK virus infection in kidney transplant recipients
title_full_unstemmed Usefulness of BK virus-specific interferon-γ enzyme-linked immunospot assay for predicting the outcome of BK virus infection in kidney transplant recipients
title_short Usefulness of BK virus-specific interferon-γ enzyme-linked immunospot assay for predicting the outcome of BK virus infection in kidney transplant recipients
title_sort usefulness of bk virus-specific interferon-γ enzyme-linked immunospot assay for predicting the outcome of bk virus infection in kidney transplant recipients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820663/
https://www.ncbi.nlm.nih.gov/pubmed/32241081
http://dx.doi.org/10.3904/kjim.2019.339
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