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Viral Infections in HSCT Recipients with Post-Transplant Lymphoproliferative Disorder: The Role of Torque Teno Virus as a Marker of Immune Functions
被引:0
|作者:
Pociupany, Martyna
[1
]
Tarabella, Carolina
[2
]
Snoeck, Robert
[1
]
Dierickx, Daan
[3
,4
]
Andrei, Graciela
[1
]
机构:
[1] Katholieke Univ Leuven, Rega Inst Med Res, Dept Microbiol Immunol & Transplantat, Mol Struct & Translat Virol Res Grp, B-3000 Leuven, Belgium
[2] Katholieke Univ Leuven, Dept Cardiovasc Sci, Ctr Mol & Vasc Biol, B-3000 Leuven, Belgium
[3] Univ Hosp Leuven, Dept Hematol, B-3000 Leuven, Belgium
[4] Katholieke Univ Leuven, Dept Oncol, Lab Expt Hematol, B-3000 Leuven, Belgium
关键词:
post-transplant lymphoproliferative disorder;
Torque Teno virus;
hematopoietic stem cell transplantation;
Epstein-Barr virus;
STEM-CELL TRANSPLANTATION;
TORQUETENOVIRUS VIREMIA;
DYNAMICS;
KINETICS;
RISK;
LOAD;
D O I:
10.3390/microorganisms13020326
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Monitoring immune function in post-transplant patients is crucial to reduce the risk of viral infections (e.g., cytomegalovirus [CMV] or Epstein-Barr virus [EBV]), which can lead to serious complications such as post-transplant lymphoproliferative disorder (PTLD). Recently, Torque Teno virus (TTV) has attracted interest as a marker of immune function. Thus, we studied the kinetics of common post-transplant viral infections (TTV, EBV, CMV, human herpesvirus-6 [HHV-6], and adenovirus [AdV]) and their association with clinical parameters in 23 HSCT recipients who developed PTLD (PTLD-HSCT) and 25 post-HSCT patients without PTLD (Non-PTLD-HSCT) at three different timepoints: at the time of the transplant (T0), 3 months (T1), and 6 months (T2) post-HSCT. Additionally, 25 healthy donors (HD) were used as the control. EBV, CMV, HHV-6, or AdV infections were found in a few samples, while TTV was found in all of our samples. The highest TTV levels (4.61 [T0], 6.24 [T1] and 6.70 [T2] log10 copies/mL) were seen in PTLD-HSCT patients compared to Non-PTLD-HSCT (3.39 [T0], 4.86 [T1], and 3.75 [T2] log10 copies/mL) and HD (2.25 log10 copies/mL) at all timepoints. Higher TTV levels were also seen in patients with a destructive type of PTLD and in surviving PTLD-HSCT patients compared to deceased ones. TTV kinetics in PTLD patients post-HSCT showed that TTV levels increase with the fall in the host immunocompetence and that by monitoring TTV kinetics, the immune status of the patient can be monitored.
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