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863. ELISpot-BK virus assay for the assesment of BK virus cell-mediated immunity in kidney recipients
BACKGROUND: The pre and post-transplant monitoring of BKV-specific T cells could be a useful marker to identify renal receptors at risk of BKV reactivation and consequently develop BKV nephropathy. METHODS: We performed a prospective multicenter study between October 2020 and December 2021. BKV-ELIS...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677160/ http://dx.doi.org/10.1093/ofid/ofad500.908 |
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author | Herrera, Sabina Sempere, Abiu Egri, Natalia Maurandi, Javier Bernal Cofan, Frederic Marcos, María Angeles Pascal, Mariona Bodro, Marta |
author_facet | Herrera, Sabina Sempere, Abiu Egri, Natalia Maurandi, Javier Bernal Cofan, Frederic Marcos, María Angeles Pascal, Mariona Bodro, Marta |
author_sort | Herrera, Sabina |
collection | PubMed |
description | BACKGROUND: The pre and post-transplant monitoring of BKV-specific T cells could be a useful marker to identify renal receptors at risk of BKV reactivation and consequently develop BKV nephropathy. METHODS: We performed a prospective multicenter study between October 2020 and December 2021. BKV-ELISPOT was performed before and two months after kidney transplantation in included patients. Other variables such as demographic, immunosuppressive therapy, presence of biopsy-proven rejection, lymphopenia, CD4 count levels and development of BK infection and nephropathy were prospectively recorded. RESULTS: We included 66 patients during the study period of whom median age was 56 (SD 16) and 60% were men. Twenty-nine percent of them received a prior transplantation, 17% was a living donor and 74% needed haemodialysis prior transplantation. Ninety-two percent received induction therapy and 86% maintenance therapy was with 3 drugs. Fifty-one percent of patients presented lymphopenia at 2 months post transplantation with a median CD4 count levels of 298 (IQR 176-899). Prior transplantation 30% of patients presented a reactive ELISPOT-BKV test, whereas at 2 months post transplantation only 21% of them tested positive. Five patients presented a BK infection and 2 of them a BK nephropathy, all of them presenting with impaired graft function at one year post transplantation.Twenty-eight percent of them presented a biopsy-proven acute rejection. All patients that presented a BKV infection presented a non-reactive ELISPOT-BKV test prior transplantation and at 2 months post transplantation. After performing multivariate analysis, neither lymphopenia, acute allograft rejection nor ELISPOT-BKV test were related to BKV infection, probably due to low incidence of BKV infection in this subgroup of kidney recipients. CONCLUSION: BKV-ELISPOT test could be a valuable tool to predict BKV infection or nephropathy and could be useful to implement preventive measures such pre-emptive reduction of immunosuppressive therapy in kidney recipients. DISCLOSURES: All Authors: No reported disclosures |
format | Online Article Text |
id | pubmed-10677160 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106771602023-11-27 863. ELISpot-BK virus assay for the assesment of BK virus cell-mediated immunity in kidney recipients Herrera, Sabina Sempere, Abiu Egri, Natalia Maurandi, Javier Bernal Cofan, Frederic Marcos, María Angeles Pascal, Mariona Bodro, Marta Open Forum Infect Dis Abstract BACKGROUND: The pre and post-transplant monitoring of BKV-specific T cells could be a useful marker to identify renal receptors at risk of BKV reactivation and consequently develop BKV nephropathy. METHODS: We performed a prospective multicenter study between October 2020 and December 2021. BKV-ELISPOT was performed before and two months after kidney transplantation in included patients. Other variables such as demographic, immunosuppressive therapy, presence of biopsy-proven rejection, lymphopenia, CD4 count levels and development of BK infection and nephropathy were prospectively recorded. RESULTS: We included 66 patients during the study period of whom median age was 56 (SD 16) and 60% were men. Twenty-nine percent of them received a prior transplantation, 17% was a living donor and 74% needed haemodialysis prior transplantation. Ninety-two percent received induction therapy and 86% maintenance therapy was with 3 drugs. Fifty-one percent of patients presented lymphopenia at 2 months post transplantation with a median CD4 count levels of 298 (IQR 176-899). Prior transplantation 30% of patients presented a reactive ELISPOT-BKV test, whereas at 2 months post transplantation only 21% of them tested positive. Five patients presented a BK infection and 2 of them a BK nephropathy, all of them presenting with impaired graft function at one year post transplantation.Twenty-eight percent of them presented a biopsy-proven acute rejection. All patients that presented a BKV infection presented a non-reactive ELISPOT-BKV test prior transplantation and at 2 months post transplantation. After performing multivariate analysis, neither lymphopenia, acute allograft rejection nor ELISPOT-BKV test were related to BKV infection, probably due to low incidence of BKV infection in this subgroup of kidney recipients. CONCLUSION: BKV-ELISPOT test could be a valuable tool to predict BKV infection or nephropathy and could be useful to implement preventive measures such pre-emptive reduction of immunosuppressive therapy in kidney recipients. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10677160/ http://dx.doi.org/10.1093/ofid/ofad500.908 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstract Herrera, Sabina Sempere, Abiu Egri, Natalia Maurandi, Javier Bernal Cofan, Frederic Marcos, María Angeles Pascal, Mariona Bodro, Marta 863. ELISpot-BK virus assay for the assesment of BK virus cell-mediated immunity in kidney recipients |
title | 863. ELISpot-BK virus assay for the assesment of BK virus cell-mediated immunity in kidney recipients |
title_full | 863. ELISpot-BK virus assay for the assesment of BK virus cell-mediated immunity in kidney recipients |
title_fullStr | 863. ELISpot-BK virus assay for the assesment of BK virus cell-mediated immunity in kidney recipients |
title_full_unstemmed | 863. ELISpot-BK virus assay for the assesment of BK virus cell-mediated immunity in kidney recipients |
title_short | 863. ELISpot-BK virus assay for the assesment of BK virus cell-mediated immunity in kidney recipients |
title_sort | 863. elispot-bk virus assay for the assesment of bk virus cell-mediated immunity in kidney recipients |
topic | Abstract |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677160/ http://dx.doi.org/10.1093/ofid/ofad500.908 |
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