QuantiFERON CMV Test and CMV Serostatus in Lung Transplant: Stratification Risk for Infection, Chronic and Acute Allograft Rejection

被引:0
|
作者
Solidoro, Paolo [1 ,2 ]
Sciarrone, Federico [1 ]
Sidoti, Francesca [3 ]
Patrucco, Filippo [4 ]
Zanotto, Elisa [3 ]
Boffini, Massimo [5 ]
Rinaldo, Rocco Francesco [1 ,2 ]
Bondi, Alessandro [6 ]
Albera, Carlo [1 ,2 ]
Curtoni, Antonio [6 ]
Costa, Cristina [6 ]
机构
[1] AOU Citta Salute & Sci Torino, Cardiovasc & Thorac Dept, Div Resp Med, I-10126 Turin, Italy
[2] Univ Turin, Med Sci Dept, I-10126 Turin, Italy
[3] AOU Citta Salute & Sci Torino, Dept Publ Hlth & Pediat, Div Virol, I-10126 Turin, Italy
[4] AOU Maggiore Carita Novara, Med Dept, Resp Dis Unit, I-28100 Novara, Italy
[5] Univ Turin, AOU Citta Salute & Sci Torino, Surg Sci Dept, Cardiac Surg Div, I-10126 Turin, Italy
[6] Univ Turin, AOU Citta Salute & Sci Torino, Dept Publ Hlth & Pediat, Div Virol, I-10126 Turin, Italy
来源
VIRUSES-BASEL | 2024年 / 16卷 / 08期
关键词
lung transplantation; CMV; cytomegalovirus; QuantiFERON; rejection; CELL-MEDIATED-IMMUNITY; BRONCHIOLITIS-OBLITERANS-SYNDROME; CYTOMEGALOVIRUS DISEASE; PROPHYLAXIS; REPLICATION; MANAGEMENT; THERAPY;
D O I
10.3390/v16081251
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The QuantiFERON CMV (QCMV) test evaluates specific adaptive immune system activity against CMV by measuring IFN-gamma released by activated CD8+ T lymphocytes. We aimed to evaluate the QCMV test as a predictive tool for CMV manifestations and acute or chronic lung allograft rejection (AR and CLAD) in lung transplant (LTx) patients. A total of 73 patients were divided into four groups based on donor and recipient (D/R) serology for CMV and QCMV assay: group A low-risk for CMV infection and disease (D-/R-); group B and C at intermediate-risk (R+), group B with non-reactive QCMV and group C with reactive QCMV; group D at high-risk (D+/R-). Group D patients experienced higher viral replication; no differences were observed among R+ patients of groups B and C. D+/R- patients had a higher number of AR events and group C presented a lower incidence of AR. Prevalence of CLAD at 24 months was higher in group B with a higher risk of CLAD development (OR 6.33). The QCMV test allows us to identify R+ non-reactive QCMV population as the most exposed to onset of CLAD. This population had a higher, although non-significant, susceptibility to AR compared to the R+ population with reactive QCMV.
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页数:10
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