Pre-transplant end-stage renal disease-related immune risk profile in kidney transplant recipients predicts post-transplant infections

被引:30
|
作者
Crepin, T. [1 ,2 ,3 ,4 ]
Gaiffe, E. [4 ,5 ]
Courivaud, C. [1 ,2 ,3 ,4 ]
Roubiou, C. [2 ,3 ,4 ]
Laheurte, C. [1 ,6 ]
Moulin, B. [7 ]
Frimat, L. [8 ]
Rieu, P. [9 ]
Mousson, C. [10 ]
Durrbach, A. [11 ]
Heng, A. -E. [12 ]
Saas, P. [1 ,2 ,3 ,5 ,6 ]
Bamoulid, J. [1 ,2 ,3 ,4 ]
Ducloux, D. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Federat Hospitalouniv INCREASE, INSERM, UMR1098, Besancon, France
[2] Univ Franche Comte, Fac Med & Pharm, Besancon, France
[3] Struct Federat Rech, SFR FED4234, Besancon, France
[4] CHU Besancon, Dept Nephrol Dialysis & Renal Transplantat, F-25030 Besancon, France
[5] CHU Besancon, CIC Biotherapie, INSERM, CIC1431, Besancon, France
[6] EFS Bourgogne Franche Comte, CIC 1431, UMR1098, Plateforme Biomonitoring, Besancon, France
[7] CHU Strasbourg, Dept Nephrol Dialysis & Renal Transplantat, Strasbourg, France
[8] CHU Nancy, Dept Nephrol Dialysis & Renal Transplantat, Nancy, France
[9] CHU Reims, Dept Nephrol Dialysis & Renal Transplantat, Reims, France
[10] CHU Dijon, Dept Nephrol Dialysis & Renal Transplantat, Dijon, France
[11] CHU Kremlin Bicetre, Dept Nephrol Dialysis & Renal Transplantat, Le Kremlin Bicetre, France
[12] CHU Clermont Ferrand, Dept Nephrol Dialysis & Renal Transplantat, Clermont Ferrand, France
关键词
transplantation; immune risk phenotype; infection; CMV; immune senescence; T-LYMPHOCYTE SUBPOPULATIONS; LONGITUDINAL OCTO-IMMUNE; CYTOMEGALOVIRUS EXPOSURE; ALLOGRAFT-REJECTION; CELLS; OLD; PROLIFERATION; POPULATION; PARAMETERS; SURVIVAL;
D O I
10.1111/tid.12534
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
BackgroundEnd-stage renal disease (ESRD) is associated with premature aging of the T-cell system. Nevertheless, the clinical significance of pre-transplant ESRD-related immune senescence is unknown. MethodsWe studied whether immune risk phenotype (IRP), a typical feature of immune senescence, may affect post-transplant infectious complications. A total of 486 patients were prospectively studied during the first year post transplant. IRP was defined as positive cytomegalovirus serology with at least 1 of the following criteria: CD4/CD8 ratio <1 and/or CD8 T-cell count >90th percentile. ResultsWe found that 47 patients (9.7%) had pre-transplant IRP. IRP+ patients did not differ from IRP- patients for any clinical characteristics, but exhibited more pronounced immune senescence. Both opportunistic infections (43% vs. 6%, P < 0.001) and severe bacterial infection (SBI) (40% vs. 25%, P = 0.028) were more frequent in IRP+ patients. In multivariate analysis, IRP was predictive of both opportunistic infection (hazard ratio [HR] 2.97 [95% confidence interval {CI} 1.53-5.76], P = 0.001), and SBI (HR 2.33 [95% CI 1.34-3.92], P = 0.008). Acute rejection rates were numerically much lower in IRP+ patients. A total of 418 patients (86%) had biological evaluation 1 year post transplant. Among 41 IRP+ patients, 35 (85%) remained IRP+ 1 year post transplant. ConclusionPre-transplant IRP is associated with an increased risk of post-transplant infection.
引用
收藏
页码:415 / 422
页数:8
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