Interactions of TTV with BKV, CMV, EBV, and HHV-6A and their impact on post-transplant graft function in kidney transplant recipients.

BKV CMV Epstein–Barr virus (EBV) HHV-6A KTx TTV

Journal

Frontiers in transplantation
ISSN: 2813-2440
Titre abrégé: Front Transplant
Pays: Switzerland
ID NLM: 9918573988006676

Informations de publication

Date de publication:
2024
Historique:
received: 29 02 2024
accepted: 24 05 2024
medline: 12 7 2024
pubmed: 12 7 2024
entrez: 12 7 2024
Statut: epublish

Résumé

Mono and combined reactivation of latent viruses occurs frequently under immunosuppressive therapy in kidney transplant patients. Recently, monitoring torque teno virus (TTV) reactivation came more into focus as a potential biomarker for immune status. The surrogate characteristics of TTV reactivation on acute rejection, and the combined reactivation with other latent viruses such as cytomegalovirus (CMV), human BK virus (BKV), Epstein-Barr virus (EBV), and human herpes virus-6A (HHV-6A) on allograft function, are unknown so far. Blood samples from 93 kidney transplant recipients obtained during the first post-transplant year were analyzed for TTV/BKV/CMV/EBV/HHV-6A load. Clinical characteristics, including graft function [glomerular filtration rate (GFR)], were collected in parallel. TTV had the highest prevalence and viral loads at 100% and a mean of 5.72 copies/ml (cp/ml) (log We were able to observe and support previously introduced TTV load thresholds predicting kidney allograft rejection. However, due to a possible delayed relation between immunosuppressive medication and TTV viral load adaptation, the right time points to start using TTV as a biomarker might need to be further clarified by other and better designed studies.

Sections du résumé

Background UNASSIGNED
Mono and combined reactivation of latent viruses occurs frequently under immunosuppressive therapy in kidney transplant patients. Recently, monitoring torque teno virus (TTV) reactivation came more into focus as a potential biomarker for immune status. The surrogate characteristics of TTV reactivation on acute rejection, and the combined reactivation with other latent viruses such as cytomegalovirus (CMV), human BK virus (BKV), Epstein-Barr virus (EBV), and human herpes virus-6A (HHV-6A) on allograft function, are unknown so far.
Methods UNASSIGNED
Blood samples from 93 kidney transplant recipients obtained during the first post-transplant year were analyzed for TTV/BKV/CMV/EBV/HHV-6A load. Clinical characteristics, including graft function [glomerular filtration rate (GFR)], were collected in parallel.
Results UNASSIGNED
TTV had the highest prevalence and viral loads at 100% and a mean of 5.72 copies/ml (cp/ml) (log
Conclusion UNASSIGNED
We were able to observe and support previously introduced TTV load thresholds predicting kidney allograft rejection. However, due to a possible delayed relation between immunosuppressive medication and TTV viral load adaptation, the right time points to start using TTV as a biomarker might need to be further clarified by other and better designed studies.

Identifiants

pubmed: 38993745
doi: 10.3389/frtra.2024.1393838
pmc: PMC11235294
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1393838

Informations de copyright

© 2024 Rosiewicz, Blazquez-Navarro, Kaliszczyk, Bauer, Or-Guil, Viebahn, Zgoura, Reinke, Roch, Hugo, Westhoff, Thieme, Stervbo and Babel.

Déclaration de conflit d'intérêts

CB was employed by MicroDiscovery GmbH. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. PR and NB declared that they were editorial board members of Frontiers at the time of submission. This had no impact on the peer review process and the final decision.

Auteurs

Kamil S Rosiewicz (KS)

Berlin Center for Advanced Therapies (BeCAT), Charité - Universitätsmedizin Berlin, Berlin, Germany.

Arturo Blazquez-Navarro (A)

Berlin Center for Advanced Therapies (BeCAT), Charité - Universitätsmedizin Berlin, Berlin, Germany.
Center for Translational Medicine, Universitätsklinikum der Ruhr-Universität Bochum, Medizinische Klinik I, Herne, Germany.

Sviatlana Kaliszczyk (S)

Berlin Center for Advanced Therapies (BeCAT), Charité - Universitätsmedizin Berlin, Berlin, Germany.
Center for Translational Medicine, Universitätsklinikum der Ruhr-Universität Bochum, Medizinische Klinik I, Herne, Germany.

Chris Bauer (C)

MicroDiscovery GmbH, Berlin, Germany.

Michal Or-Guil (M)

Institute of Medical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Richard Viebahn (R)

Chirurgische Klinik, Universitätsklinikum Knappschaftskrankenhaus Bochum, Bochum, Germany.

Panagiota Zgoura (P)

Chirurgische Klinik, Universitätsklinikum Knappschaftskrankenhaus Bochum, Bochum, Germany.

Petra Reinke (P)

Berlin Center for Advanced Therapies (BeCAT), Charité - Universitätsmedizin Berlin, Berlin, Germany.

Toralf Roch (T)

Berlin Center for Advanced Therapies (BeCAT), Charité - Universitätsmedizin Berlin, Berlin, Germany.

Christian Hugo (C)

Universitätsklinikum Carl Gustav Carus, Medizinische Klinik III - Bereich Nephrologie, Dresden, Germany.

Timm Westhoff (T)

Center for Translational Medicine, Universitätsklinikum der Ruhr-Universität Bochum, Medizinische Klinik I, Herne, Germany.

Constantin Thieme (C)

Berlin Center for Advanced Therapies (BeCAT), Charité - Universitätsmedizin Berlin, Berlin, Germany.

Ulrik Stervbo (U)

Berlin Center for Advanced Therapies (BeCAT), Charité - Universitätsmedizin Berlin, Berlin, Germany.
Center for Translational Medicine, Universitätsklinikum der Ruhr-Universität Bochum, Medizinische Klinik I, Herne, Germany.

Nina Babel (N)

Berlin Center for Advanced Therapies (BeCAT), Charité - Universitätsmedizin Berlin, Berlin, Germany.
Center for Translational Medicine, Universitätsklinikum der Ruhr-Universität Bochum, Medizinische Klinik I, Herne, Germany.

Classifications MeSH