Author:
Kamali Kaan,Schmelzle Moritz,Kamali Can,Brunnbauer Philipp,Splith Katrin,Leder Annekatrin,Berndt Nadja,Hillebrandt Karl-Herbert,Raschzok Nathanael,Feldbrügge Linda,Felsenstein Matthäus,Gaßner Joseph,Ritschl Paul,Lurje Georg,Schöning Wenzel,Benzing Christian,Pratschke Johann,Krenzien Felix
Abstract
Acute cellular rejection (ACR) after liver transplantation (LT) goes along with allograft dysfunction, which is diagnosed by liver biopsy and concomitant histological analysis, representing the gold standard in clinical practice. Yet, liver biopsies are invasive, costly, time-intensive and require expert knowledge. Herein we present substantial evidence that blood plasma residing peripheral liver-derived extracellular particles (EP) could be employed to diagnose ACR non-invasively. In vitro experiments showed organ-specific EP release from primary human hepatocytes under immunological stress. Secondly, analysis of consecutive LT patients (n=11) revealed significant heightened EP concentrations days before ACR. By conducting a diagnostic accuracy study (n = 69, DRKS00011631), we explored the viability of using EP as a liquid biopsy for diagnosing ACR following LT. Consequently, novel EP populations in samples were identified using visualization of t-distributed stochastic neighbor embedding (viSNE) and self-organizing maps (FlowSOM) algorithms. As a result, the ASGR1+CD130+Annexin V+ EP subpopulation exhibited the highest accuracy for predicting ACR (area under the curve: 0.80, 95% confidence interval [CI], 0.70–0.90), with diagnostic sensitivity and specificity of 100% (95% CI, 81.67–100.0%) and 68.5% (95% CI, 55.3–79.3%), respectively. In summary, this new EP subpopulation presented the highest diagnostic accuracy for detecting ACR in LT patients.
Funder
Deutsche Forschungsgemeinschaft
Bundesministerium für Wirtschaft und Technologie
Subject
Immunology,Immunology and Allergy
Cited by
4 articles.
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