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An Analysis of Regulatory T-Cell and Th-17 Cell Dynamics during Cytomegalovirus Replication in Solid Organ Transplant Recipients
被引:37
作者:
Egli, Adrian
[1
,2
]
Silva, Moacyr, Jr.
[1
,2
]
O'Shea, Daire
[1
,2
]
Wilson, Leticia E.
[1
,2
]
Baluch, Aliyah
[1
,2
]
Lisboa, Luiz F.
[1
,2
]
Hidalgo, Luis G.
[3
]
Kumar, Deepali
[1
,2
]
Humar, Atul
[1
,2
]
机构:
[1] Univ Alberta, Alberta Transplant Inst, Edmonton, AB, Canada
[2] Univ Alberta, Li Ka Shing Inst Virol, Edmonton, AB, Canada
[3] Univ Alberta, Dept Lab Med & Pathol, Histocompatibil Lab, Edmonton, AB, Canada
来源:
PLOS ONE
|
2012年
/
7卷
/
10期
基金:
瑞士国家科学基金会;
关键词:
VIRUS-INFECTION;
CMV DISEASE;
TH17;
CELLS;
PERIPHERAL-BLOOD;
HIGH-RISK;
IMMUNITY;
RESPONSES;
IMMUNOPATHOLOGY;
TOLERANCE;
REJECTION;
D O I:
10.1371/journal.pone.0043937
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
CMV-specific T-cells are crucial to control CMV-replication post-transplant. Regulatory T-cells (T-regs) are associated with a tolerant immune state and may contribute to CMV-replication. However, T-cell subsets such as T-regs and IL-17 producing T-cells (Th-17) are not well studied in this context. We explored T-regs and Th-17 frequencies during CMV-replication after transplantation. Methods: We prospectively evaluated 30 transplant patients with CMV-viremia. We quantified CMV-specific CD4(+) and CD8(+) T-cells, T-regs (CD4(+) CD25(+) FoxP3(+)) and Th-17 frequencies using flow-cytometry and followed patients requiring anti-viral treatment. Two subsets were compared: anti-viral treatment requirement (n = 20) vs. spontaneous clearance of viremia (n = 10). Results: Higher initial CMV-specific CD4(+) T-cells and lower T-regs were observed in patients with spontaneous clearance (p = 0.043; p = 0.021 respectively). Using a ratio of CMV-specific CD4(+) T-cells to T-regs allowed prediction of viral clearance with 80% sensitivity and 90% specificity (p = 0.001). One month after stop of treatment, the same correlation was observed in patients protected from CMV-relapse. The ratio of CMV-specific CD4(+) T-cells to T-regs allowed prediction of relapse with 85% sensitivity and 86% specificity (p = 0.004). Th-17 responses were not correlated with virologic outcomes. Conclusions: This study provides novel insights into T-regs and Th-17 subpopulations during CMV-replication after transplantation. These preliminary data suggest that measurement of CMV-specific CD4(+) T-cells together with T-regs has value in predicting spontaneous clearance of viremia and relapse.
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