Donor-specific antibodies: Can they predict C4d deposition in pediatric heart recipients?

被引:13
作者
Peng, David M. [1 ]
Law, Yuk M. [1 ]
Kemna, Mariska S. [1 ]
Warner, Paul [2 ]
Nelson, Karen [2 ]
Boucek, Robert J. [1 ]
机构
[1] Univ Washington, Seattle Childrens Hosp, Seattle, WA 98195 USA
[2] Puget Sound Blood Ctr, Seattle, WA 98104 USA
关键词
antibody mediated rejection; anti-HLA antibody; pediatric heart transplant; biopsy; heart transplantation; SOLID-ORGAN TRANSPLANTATION; CORONARY-ARTERY-DISEASE; MEDIATED REJECTION; HLA ANTIBODIES; CARDIOVASCULAR MORTALITY; ENDOMYOCARDIAL BIOPSY; HUMORAL REJECTION; CROSS-MATCH; ALLOGRAFT; SURVEILLANCE;
D O I
10.1111/petr.12075
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
There is limited evidence regarding the utility of circulating DSA in surveillance for AMR of pediatric heart recipients. Our hypothesis is that quantitation of DSA improves their power for predicting a C4d+, an integral component in the current diagnostic criteria of AMR. All pediatric recipients transplanted between 10/2005 and 1/2011 were retrospectively reviewed for DSA determined within 48h of EMB. C4d+ was defined as >25% endothelial cell staining by immunohistochemical methods. A total of 183 paired DSA-EMB determinations were identified in 60 patients, a median of three paired studies per patient (range: 1-9). DSA were detected in 60 of these determinations. A receiver-operating characteristic plot identified a threshold single-antibody MFI of >6000 that strongly correlated with C4d+ (p<0.0001) with a high negative predictive value (0.97) and specificity (0.95). The sensitivity and positive predictive values were 0.71 and 0.60, respectively. The predictive power of single-antigen DSA for C4d deposition was improved in pediatric heart recipients using an institution-specific MFI threshold value. In post-transplant care, quantitative DSA should be an essential component in the surveillance for AMR.
引用
收藏
页码:429 / 435
页数:7
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