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Predictive Potential of Flow Cytometry Crossmatching in Deceased Donor Kidney Transplant Recipients Subjected to Peritransplant Desensitization
K. Osickova, P. Hruba, K. Kabrtova, J. Klema, J. Maluskova, A. Slavcev, J. Slatinska, T. Marada, GA. Böhmig, O. Viklicky
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 2014
Free Medical Journals
od 2014
PubMed Central
od 2014
Europe PubMed Central
od 2014
Open Access Digital Library
od 2014-01-01
Open Access Digital Library
od 2014-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2014
PubMed
34970564
DOI
10.3389/fmed.2021.780636
Knihovny.cz E-zdroje
- Publikační typ
- časopisecké články MeSH
Recipient sensitization is a major risk factor of antibody-mediated rejection (ABMR) and inferior graft survival. The predictive effect of solid-phase human leukocyte antigen antibody testing and flow cytometry crossmatch (FCXM) in the era of peritransplant desensitization remains poorly understood. This observational retrospective single-center study with 108 donor-specific antibody (DSA)-positive deceased donor kidney allograft recipients who had undergone peritransplant desensitization aimed to analyze variables affecting graft outcome. ABMR rates were highest among patients with positive pretransplant FCXM vs. FCXM-negative (76 vs. 18.7%, p < 0.001) and with donor-specific antibody mean fluorescence intensity (DSA MFI) > 5,000 vs. <5,000 (54.5 vs. 28%, p = 0.01) despite desensitization. In univariable Cox regression, FCXM positivity, retransplantation, recipient gender, immunodominant DSA MFI, DSA number, and peak panel reactive antibodies were found to be associated with ABMR occurrence. In multivariable Cox regression adjusted for desensitization treatment (AUC = 0.810), only FCXM positivity (HR = 4.6, p = 0.001) and DSA number (HR = 1.47, p = 0.039) remained significant. In conclusion, our data suggest that pretransplant FCXM and DSA number, but not DSA MFI, are independent predictors of ABMR in patients who received peritransplant desensitization.
Aesculab Pathology Prague Czechia
Department of Immunogenetics Institute for Clinical and Experimental Medicine Prague Czechia
Department of Nephrology Institute for Clinical and Experimental Medicine Prague Czechia
Department of Pathology Institute for Clinical and Experimental Medicine Prague Czechia
Department of Transplant Surgery Institute for Clinical and Experimental Medicine Prague Czechia
Transplant Laboratory Institute for Clinical and Experimental Medicine Prague Czechia
Citace poskytuje Crossref.org
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