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Torque teno viral load reflects immunosuppression in paediatric kidney-transplanted patients—a pilot study
BACKGROUND: Chronic deterioration of kidney graft function is related to inadequate immunosuppression (IS). A novel tool to assess the individual net state of IS in transplanted patients might be the monitoring of Torque teno virus (TTV) viral load. TTV is a non-pathogen virus detectable in almost a...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7701084/ https://www.ncbi.nlm.nih.gov/pubmed/32524259 http://dx.doi.org/10.1007/s00467-020-04606-3 |
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author | Uhl, Phoebe Heilos, Andreas Bond, Gregor Meyer, Elias Böhm, Michael Puchhammer-Stöckl, Elisabeth Arbeiter, Klaus Müller-Sacherer, Thomas Csaicsich, Dagmar Aufricht, Christoph Rusai, Krisztina |
author_facet | Uhl, Phoebe Heilos, Andreas Bond, Gregor Meyer, Elias Böhm, Michael Puchhammer-Stöckl, Elisabeth Arbeiter, Klaus Müller-Sacherer, Thomas Csaicsich, Dagmar Aufricht, Christoph Rusai, Krisztina |
author_sort | Uhl, Phoebe |
collection | PubMed |
description | BACKGROUND: Chronic deterioration of kidney graft function is related to inadequate immunosuppression (IS). A novel tool to assess the individual net state of IS in transplanted patients might be the monitoring of Torque teno virus (TTV) viral load. TTV is a non-pathogen virus detectable in almost all individuals. TTV level in the peripheral blood has been linked to the immune-competence of its host and should thus reflect IS after solid organ transplantation. METHODS: TTV plasma load was quantified monthly by RT-PCR for a period of 1 year in 45 kidney-transplanted children. Post-transplant time was at least 3 months. The relation of the virus DNA levels to IS and transplant-specific clinical and laboratory parameters was analysed longitudinally. RESULTS: TTV DNA was detectable in 94.5% of the plasma samples. There was a significant association with the post-transplant follow-up time as well as with the type of IS regimen, with lower virus loads in patients after longer post-transplant time and mTOR inhibitor–based IS. Furthermore, a significant positive correlation with the dose of prednisolone and mycophenolate mofetil was found. CONCLUSIONS: TTV levels show an association/correlation with the strength of IS. Further studies are needed in order to evaluate TTV measurement as a tool for IS monitoring for hard clinical outcomes such as presence of donor-specific antibodies, rejections or infections—common consequences of insufficient or too intense IS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00467-020-04606-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7701084 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-77010842020-12-03 Torque teno viral load reflects immunosuppression in paediatric kidney-transplanted patients—a pilot study Uhl, Phoebe Heilos, Andreas Bond, Gregor Meyer, Elias Böhm, Michael Puchhammer-Stöckl, Elisabeth Arbeiter, Klaus Müller-Sacherer, Thomas Csaicsich, Dagmar Aufricht, Christoph Rusai, Krisztina Pediatr Nephrol Original Article BACKGROUND: Chronic deterioration of kidney graft function is related to inadequate immunosuppression (IS). A novel tool to assess the individual net state of IS in transplanted patients might be the monitoring of Torque teno virus (TTV) viral load. TTV is a non-pathogen virus detectable in almost all individuals. TTV level in the peripheral blood has been linked to the immune-competence of its host and should thus reflect IS after solid organ transplantation. METHODS: TTV plasma load was quantified monthly by RT-PCR for a period of 1 year in 45 kidney-transplanted children. Post-transplant time was at least 3 months. The relation of the virus DNA levels to IS and transplant-specific clinical and laboratory parameters was analysed longitudinally. RESULTS: TTV DNA was detectable in 94.5% of the plasma samples. There was a significant association with the post-transplant follow-up time as well as with the type of IS regimen, with lower virus loads in patients after longer post-transplant time and mTOR inhibitor–based IS. Furthermore, a significant positive correlation with the dose of prednisolone and mycophenolate mofetil was found. CONCLUSIONS: TTV levels show an association/correlation with the strength of IS. Further studies are needed in order to evaluate TTV measurement as a tool for IS monitoring for hard clinical outcomes such as presence of donor-specific antibodies, rejections or infections—common consequences of insufficient or too intense IS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00467-020-04606-3) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-06-10 2021 /pmc/articles/PMC7701084/ /pubmed/32524259 http://dx.doi.org/10.1007/s00467-020-04606-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Article Uhl, Phoebe Heilos, Andreas Bond, Gregor Meyer, Elias Böhm, Michael Puchhammer-Stöckl, Elisabeth Arbeiter, Klaus Müller-Sacherer, Thomas Csaicsich, Dagmar Aufricht, Christoph Rusai, Krisztina Torque teno viral load reflects immunosuppression in paediatric kidney-transplanted patients—a pilot study |
title | Torque teno viral load reflects immunosuppression in paediatric kidney-transplanted patients—a pilot study |
title_full | Torque teno viral load reflects immunosuppression in paediatric kidney-transplanted patients—a pilot study |
title_fullStr | Torque teno viral load reflects immunosuppression in paediatric kidney-transplanted patients—a pilot study |
title_full_unstemmed | Torque teno viral load reflects immunosuppression in paediatric kidney-transplanted patients—a pilot study |
title_short | Torque teno viral load reflects immunosuppression in paediatric kidney-transplanted patients—a pilot study |
title_sort | torque teno viral load reflects immunosuppression in paediatric kidney-transplanted patients—a pilot study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7701084/ https://www.ncbi.nlm.nih.gov/pubmed/32524259 http://dx.doi.org/10.1007/s00467-020-04606-3 |
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