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Relevance of Tacrolimus Trough Concentration and Hepatitis E virus Genetic Changes in Kidney Transplant Recipients With Chronic Hepatitis E

Authors
  • León-Janampa, Nancy
  • Boennec, Natacha
  • Le Tilly, Olivier
  • Ereh, Simon
  • Herbet, Gabriel
  • Moreau, Alain
  • Gatault, Philippe
  • Longuet, Hélène
  • Barbet, Christelle
  • Büchler, Mathias
  • Baron, Christophe
  • Gaudy-Graffin, Catherine
  • Brand, Denys
  • Marlet, Julien
Publication Date
Jan 01, 2024
Identifiers
DOI: 10.1016/j.ekir.2024.01.054
OAI: oai:HAL:hal-04491246v1
Source
HAL-Descartes
Keywords
Language
English
License
Unknown
External links

Abstract

Introduction: Hepatitis E virus (HEV) can cause chronic infection ($3 months) and cirrhosis in immunocompromised patients, especially kidney transplant recipients. Low alanine aminotransferase (ALT) levels and high HEV intrahost diversity have previously been associated with evolution toward chronicity in these patients. We hypothesized that additional clinical and viral factors could be associated with the risk of chronic HEV infection. Methods: We investigated a series of 27 kidney transplant recipients with HEV infection, including 20 patients with chronic hepatitis E. Results: High tacrolimus trough concentration at diagnosis was the most relevant marker associated with chronic hepatitis E (9.2 vs. 6.4 ng/ml, P ¼ 0.04). Most HEV genetic changes selected during HEV infection were compartmentalized between plasma and feces. Conclusion: This compartmentalization highlights the diversity and complexity of HEV replication compartments. Tacrolimus trough concentration at diagnosis of HEV infection could allow an early identification of patients at high risk of chronic hepatitis E and guide treatment initiation.

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