Each 1-log10 increase in pre-transplant TTV load in lung recipients increased early infection risk (aOR 15.05) and 1-year graft failure (aHR 1.40), but reduced acute rejection (aHR 0.70).
Does pre-transplant Torque teno virus (TTV) load predict early post-transplant infection, acute rejection, and 1-year graft failure in lung transplant recipients?
Higher pre-transplant plasma TTV load is a strong predictor of early post-transplant infection and 1-year graft failure, but is associated with fewer acute rejection events, highlighting its potential as a biomarker for immune risk stratification.
Tasa de eventos absoluta: 0% vs 0%
AbstractBackground Torque teno virus (TTV) load has emerged as a potential surrogate marker of net immunosuppression in solid organ transplantation. However, the clinical significance of pre-transplant TTV levels for early outcomes after lung transplantation remains unclear. Methods In this multicenter cohort of 334 adult first-time lung transplant recipients (2015–2022), plasma samples were collected immediately prior to transplantation. The primary endpoint was infection within 3 months. One hundred healthy individuals served as controls for TTV comparisons. Secondary outcomes were acute rejection and 1-year graft failure. Associations were evaluated using multivariable logistic regression for early infection and time-to-event analyses for rejection and graft failure. Results Pre-transplant TTV levels were higher in recipients than in controls (6.7 vs 5.9 log₁₀ copies/mL; pConclusions Pre-transplant plasma TTV load was associated with early infection, fewer rejection events, and increased 1-year graft failure after lung transplantation, supporting its potential role as a biomarker for immune risk stratification.
Lee et al. (Sun,) reported a other. Each 1-log10 increase in pre-transplant TTV load in lung recipients increased early infection risk (aOR 15.05) and 1-year graft failure (aHR 1.40), but reduced acute rejection (aHR 0.70).
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