TTV and CMV viral load dynamics: Which emerges first during immunosuppression?

Author:

Roberto Piergiorgio123ORCID,Cinti Lilia134,Lucente Dario5,Russo Gianluca36,Lai Quirino37,Micozzi Alessandra38,Gentile Giuseppe38,Turriziani Ombretta13ORCID,Pierangeli Alessandra1ORCID,Antonelli Guido13ORCID

Affiliation:

1. Laboratory of Microbiology and Virology, Department of Molecular Medicine Sapienza University of Rome Rome Italy

2. PhD National Programme in One Health Approaches to Infectious Diseases and Life Science Research, Department of Public Health, Experimental and Forensic Medicine University of Pavia Pavia Italy

3. University Hospital “Policlinico Umberto I” Rome Italy

4. PhD National Programme in Innovazione nella diagnosi, prevenzione e terapia delle infezioni a rischio epidemico‐pandemico, Dipartimento di Biotecnologie Mediche University of Siena Siena Italy

5. Department of Mathematics & Physics University of Campania “Luigi Vanvitelli” Caserta Italy

6. Department of Public Health and Infectious Diseases Sapienza University of Rome Rome Italy

7. Department of Chirurgia Generale e Specialistica Sapienza Università di Roma Roma Italy

8. Department of Translational and Precision Medicine Sapienza University of Rome Rome Italy

Abstract

AbstractNovel biomarkers reflecting the degree of immunosuppression in transplant patients are required to ensure eventual personalized equilibrium between rejection and infection risks. With the above aim, Torque Teno Virus (TTV) viremia was precisely examined in a large cohort of transplanted immunocompromised patients (192 hematological and 60 solid organ transplant recipients) being monitored for Cytomegalovirus reactivation. TTV load was measured in 2612 plasma samples from 448 patients. The results revealed a significant increase in TTV viral load approximately 14 days following CMV reactivation/infection in solid organ transplant (SOT) patients. No recognizable difference in TTV load was noted among hematological patients during the entire timeframe analyzed. Furthermore, a temporal gap of approximately 30 days was noted between the viral load peaks reached by the two viruses, with Cytomegalovirus (CMV) preceding TTV. It was not possible to establish a correlation between CMV reactivation/infection and TTV viremia in hematological patients. On the other hand, the SOT patient cohort allowed us to analyze viral kinetics and draw intriguing conclusions. Taken together, the data suggest, to our knowledge for the first time, that CMV infection itself could potentially cause an increase in TTV load in the peripheral blood of patients undergoing immunosuppressive therapy.

Publisher

Wiley

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