Interleukin‐18 and tumor necrosis factor‐α are elevated in solid organ transplant recipients with possible cytomegalovirus end‐organ disease
End‐organ cytomegalovirus (CMV) disease can be life threatening to solid organ transplant recipients. Diagnosis is often complicated by variation in amount of CMV DNA in plasma and the need for an invasive procedure to obtain a biopsy of the suspected affected organ, which can delay recognition and...
Gespeichert in:
Veröffentlicht in: | Transplant infectious disease 2021-08, Vol.23 (4), p.e13682-n/a |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | End‐organ cytomegalovirus (CMV) disease can be life threatening to solid organ transplant recipients. Diagnosis is often complicated by variation in amount of CMV DNA in plasma and the need for an invasive procedure to obtain a biopsy of the suspected affected organ, which can delay recognition and treatment. Several inflammatory cytokines are elevated in CMV disease, and the purpose of this study was to determine if they could be used to distinguish solid organ transplant recipients with CMV DNAemia alone from those with possible end‐organ CMV disease. We found that regardless of pre‐transplant CMV serostatus, plasma interleukin (IL)‐18, tumor necrosis factor‐α (TNF‐α), and amount of CMV DNA in plasma were increased in possible end‐organ CMV disease, with elevated IL‐18 associated with increased odds of possible end‐organ CMV disease even after adjusting for amount of CMV DNA. These findings highlight IL‐18 and TNF‐α as potential non‐invasive markers of possible end‐organ CMV disease regardless of transplanted organ or serostatus in solid organ transplant recipients. |
---|---|
ISSN: | 1398-2273 1399-3062 |
DOI: | 10.1111/tid.13682 |