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 al...

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Veröffentlicht in:Pediatric nephrology (Berlin, West) West), 2021-01, Vol.36 (1), p.153-162
Hauptverfasser: Uhl, Phoebe, Heilos, Andreas, Bond, Gregor, Meyer, Elias, Böhm, Michael, Puchhammer-Stöckl, Elisabeth, Arbeiter, Klaus, Müller-Sacherer, Thomas, Csaicsich, Dagmar, Aufricht, Christoph, Rusai, Krisztina
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Sprache:eng
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Zusammenfassung: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.
ISSN:0931-041X
1432-198X
DOI:10.1007/s00467-020-04606-3