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Immune monitoring of prevalent kidney transplant recipients using Torque Teno Virus: Protocol for a single-centre prospective cohort study

INTRODUCTION: Kidney transplant recipients (KTRs) suffer from immunosuppression-related adverse events (iRAEs), such as infections and malignancy from chronic immunosuppression, but are also at risk of graft loss from rejection with underimmunosuppression. Biomarkers that predict both iRAEs and reje...

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Autores principales: Ho, Quan Yao, Lai, Chooi Mun Deborah, Liew, Ian Tatt, Oon, Lynette Lin Ean, Lim, Kun Lee, Chung, Shimin Jasmine, Thangaraju, Sobhana, Tien, Shan-Yeu Carolyn, Tan, Chieh Suai, Kee, Terence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510931/
https://www.ncbi.nlm.nih.gov/pubmed/37730403
http://dx.doi.org/10.1136/bmjopen-2023-076122
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author Ho, Quan Yao
Lai, Chooi Mun Deborah
Liew, Ian Tatt
Oon, Lynette Lin Ean
Lim, Kun Lee
Chung, Shimin Jasmine
Thangaraju, Sobhana
Tien, Shan-Yeu Carolyn
Tan, Chieh Suai
Kee, Terence
author_facet Ho, Quan Yao
Lai, Chooi Mun Deborah
Liew, Ian Tatt
Oon, Lynette Lin Ean
Lim, Kun Lee
Chung, Shimin Jasmine
Thangaraju, Sobhana
Tien, Shan-Yeu Carolyn
Tan, Chieh Suai
Kee, Terence
author_sort Ho, Quan Yao
collection PubMed
description INTRODUCTION: Kidney transplant recipients (KTRs) suffer from immunosuppression-related adverse events (iRAEs), such as infections and malignancy from chronic immunosuppression, but are also at risk of graft loss from rejection with underimmunosuppression. Biomarkers that predict both iRAEs and rejection while allowing individualisation of immunosuppression exposure are lacking. Although plasma viral DNA levels of torque teno virus (TTV), a widely prevalent, non-pathogenic virus, have been shown to predict both iRAE and rejection in newly transplanted KTRs within the first year after transplant, its role for prevalent KTRs on stable immunosuppression is less clear. This study aims to determine the prognostic value of TTV levels for severe infections (defined as infections requiring hospitalisation) in prevalent KTRs on stable immunosuppression for at least 3 months and compare it against that of other commonly available biomarkers. The study also aims to explore the relationship between TTV levels and factors affecting the ‘net state of immunosuppression’ as well as other clinical outcomes. METHODS AND ANALYSIS: This is a single-centre, prospective, observational cohort study of 172 KTRs on stable immunosuppression for more than 3 months. TTV levels will be measured using the TTV R-GENE kit upon recruitment when study subjects are admitted and when kidney allograft biopsies are performed. Subjects will be monitored for iRAEs and rejection for at least 12 months. The relationship between TTV load and clinical outcomes such as severe infections will be analysed and compared against that from other common biomarkers and previously published predictive scores. ETHICS AND DISSEMINATION: The study was approved by the SingHealth Centralised Institutional Review Board (2023/2170). The results will be presented at conferences and submitted for publication in peer-reviewed journals. TRIAL REGISTRATION NUMBER: NCT05836636.
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spelling pubmed-105109312023-09-21 Immune monitoring of prevalent kidney transplant recipients using Torque Teno Virus: Protocol for a single-centre prospective cohort study Ho, Quan Yao Lai, Chooi Mun Deborah Liew, Ian Tatt Oon, Lynette Lin Ean Lim, Kun Lee Chung, Shimin Jasmine Thangaraju, Sobhana Tien, Shan-Yeu Carolyn Tan, Chieh Suai Kee, Terence BMJ Open Renal Medicine INTRODUCTION: Kidney transplant recipients (KTRs) suffer from immunosuppression-related adverse events (iRAEs), such as infections and malignancy from chronic immunosuppression, but are also at risk of graft loss from rejection with underimmunosuppression. Biomarkers that predict both iRAEs and rejection while allowing individualisation of immunosuppression exposure are lacking. Although plasma viral DNA levels of torque teno virus (TTV), a widely prevalent, non-pathogenic virus, have been shown to predict both iRAE and rejection in newly transplanted KTRs within the first year after transplant, its role for prevalent KTRs on stable immunosuppression is less clear. This study aims to determine the prognostic value of TTV levels for severe infections (defined as infections requiring hospitalisation) in prevalent KTRs on stable immunosuppression for at least 3 months and compare it against that of other commonly available biomarkers. The study also aims to explore the relationship between TTV levels and factors affecting the ‘net state of immunosuppression’ as well as other clinical outcomes. METHODS AND ANALYSIS: This is a single-centre, prospective, observational cohort study of 172 KTRs on stable immunosuppression for more than 3 months. TTV levels will be measured using the TTV R-GENE kit upon recruitment when study subjects are admitted and when kidney allograft biopsies are performed. Subjects will be monitored for iRAEs and rejection for at least 12 months. The relationship between TTV load and clinical outcomes such as severe infections will be analysed and compared against that from other common biomarkers and previously published predictive scores. ETHICS AND DISSEMINATION: The study was approved by the SingHealth Centralised Institutional Review Board (2023/2170). The results will be presented at conferences and submitted for publication in peer-reviewed journals. TRIAL REGISTRATION NUMBER: NCT05836636. BMJ Publishing Group 2023-09-19 /pmc/articles/PMC10510931/ /pubmed/37730403 http://dx.doi.org/10.1136/bmjopen-2023-076122 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Renal Medicine
Ho, Quan Yao
Lai, Chooi Mun Deborah
Liew, Ian Tatt
Oon, Lynette Lin Ean
Lim, Kun Lee
Chung, Shimin Jasmine
Thangaraju, Sobhana
Tien, Shan-Yeu Carolyn
Tan, Chieh Suai
Kee, Terence
Immune monitoring of prevalent kidney transplant recipients using Torque Teno Virus: Protocol for a single-centre prospective cohort study
title Immune monitoring of prevalent kidney transplant recipients using Torque Teno Virus: Protocol for a single-centre prospective cohort study
title_full Immune monitoring of prevalent kidney transplant recipients using Torque Teno Virus: Protocol for a single-centre prospective cohort study
title_fullStr Immune monitoring of prevalent kidney transplant recipients using Torque Teno Virus: Protocol for a single-centre prospective cohort study
title_full_unstemmed Immune monitoring of prevalent kidney transplant recipients using Torque Teno Virus: Protocol for a single-centre prospective cohort study
title_short Immune monitoring of prevalent kidney transplant recipients using Torque Teno Virus: Protocol for a single-centre prospective cohort study
title_sort immune monitoring of prevalent kidney transplant recipients using torque teno virus: protocol for a single-centre prospective cohort study
topic Renal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510931/
https://www.ncbi.nlm.nih.gov/pubmed/37730403
http://dx.doi.org/10.1136/bmjopen-2023-076122
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