Clinically-relevant threshold of preformed donor-specific anti-HLA antibodies in kidney transplantation

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• 作者：Igor Salvadé ; ^a ; ^{igor.salvade@chuv.ch" class="auth_mail" title="E-mail the corresponding author} ; Vincent Aubert^a ; Jean-Pierre Venetz^a ; Dela Golshayan^a ; Anne-Catherine Saouli^a ; Maurice Matter^b ; Samuel Rotman^c ; Giuseppe Pantaleo^a ; Manuel Pascual^a ; ^{manuel.pascual@chuv.ch" class="auth_mail" title="E-mail the corresponding author}
• 关键词：AIC ; Akaike&rsquo ; s information coefficient ; AMR ; antibody-mediated rejection ; CDC ; complement dependent cytotoxicity ; cMFI ; cumulative mean fluorescence intensity ; CsA ; cyclosporine ; DSA ; donor-specific antibodies ; FCXM ; flow cytometric crossmatch ; HLA ; human leukocyte antigen ; ivIg ; intravenous immunoglobulin ; MMF ; mycophenolate mofetil ; PRA ; panel reactive antibody ; SPA ; solid phase assay ; Tx ; transplantation
• 刊名：Human Immunology
• 出版年：2016
• 出版时间：June 2016
• 年：2016
• 卷：77
• 期：6
• 页码：483-489
• 全文大小：754 K

文摘

Pretransplant anti-HLA donor-specific antibodies (DSA) are recognized as a risk factor for acute antibody-mediated rejection (AMR) in kidney transplantation. The predictive value of C4d-fixing capability by DSA or of IgG DSA subclasses for acute AMR in the pretransplant setting has been recently studied. In addition DSA strength assessed by mean fluorescence intensity (MFI) may improve risk stratification. We aimed to analyze the relevance of preformed DSA and of DSA MFI values.

Methods

280 consecutive patients with negative complement-dependent cytotoxicity crossmatches received a kidney transplant between 01/2008 and 03/2014. Sera were screened for the presence of DSA with a solid-phase assays on a Luminex flow analyzer, and the results were correlated with biopsy-proven acute AMR in the first year and survival.

Results

Pretransplant anti-HLA antibodies were present in 72 patients (25.7%) and 24 (8.6%) had DSA. There were 46 (16.4%) acute rejection episodes, 32 (11.4%) being cellular and 14 (5.0%) AMR. The incidence of acute AMR was higher in patients with pretransplant DSA (41.7%) than in those without (1.6%) (p < 0.001). The median cumulative MFI (cMFI) of the group DSA+/AMR+ was 5680 vs 2208 in DSA+/AMR− (p = 0.058). With univariate logistic regression a threshold value of 5280 cMFI was predictive for acute AMR. DSA cMFI’s ability to predict AMR was also explored by ROC analysis. AUC was 0.728 and the best threshold was a cMFI of 4340. Importantly pretransplant DSA > 5280 cMFI had a detrimental effect on 5-year graft survival.

Conclusions

Preformed DSA cMFI values were clinically-relevant for the prediction of acute AMR and graft survival in kidney transplantation. A threshold of 4300–5300 cMFI was a significant outcome predictor.