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Dokumenttyp:
Journal Article
Autor(en):
Banas, Bernhard; Steubl, Dominik; Renders, Lutz; Chittka, Dominik; Banas, Miriam C; Wekerle, Thomas; Koch, Martina; Witzke, Oliver; Mühlfeld, Anja; Sommerer, Claudia; Habicht, Antje; Hugo, Christian; Hünig, Thomas; Lindemann, Monika; Schmidt, Traudel; Rascle, Anne; Barabas, Sascha; Deml, Ludwig; Wagner, Ralf; Krämer, Bernhard K; Krüger, Bernd
Titel:
Clinical validation of a novel enzyme-linked immunosorbent spot assay-based in vitro diagnostic assay to monitor cytomegalovirus-specific cell-mediated immunity in kidney transplant recipients: a multicenter, longitudinal, prospective, observational study
Abstract:
Impaired cytomegalovirus (CMV)-specific cell-mediated immunity (CMV-CMI) is a major cause of CMV reactivation and associated complications in solid-organ transplantation. Reliably assessing CMV-CMI is desirable to individually adjust antiviral and immunosuppressive therapy. This study aimed to evaluate the suitability of T-Track CMV, a novel IFN-? ELISpot assay based on the stimulation of peripheral blood mononuclear cells with pp65 and IE-I CMV proteins, to monitor CMV-CMI following kidney transplantation. A prospective longitudinal multicenter study was conducted in 86 intermediate-risk renal transplant recipients. CMV-CMI, CMV viral load, and clinical complications were monitored over 6 months post-transplantation. Ninety-five percent and 88-92% ELISpot assays were positive pre- and post-transplantation, respectively. CMV-specific response was reduced following immunosuppressive treatment and increased in patients with graft rejection, indicating the ability of the ELISpot assay to monitor patients' immunosuppressive state. Interestingly, median pp65-specific response was ninefold higher in patients with self-clearing viral load compared to antivirally treated patients prior to first viral load detection (P < 0.001), suggesting that reactivity to pp65 represents a potential immunocompetence marker. Altogether, T-Track CMV is a highly sensitive IFN-? ELISpot assay, suitable for the immunomonitoring of CMV-seropositive renal transplant recipients, and with a potential use for the risk assessment of CMV-related clinical complications (ClinicalTrials.gov Identifier: NCT02083042).
Zeitschriftentitel:
Transpl Int
Jahr:
2018
Band / Volume:
31
Heft / Issue:
4
Seitenangaben Beitrag:
436-450
Volltext / DOI:
doi:10.1111/tri.13110
PubMed:
http://view.ncbi.nlm.nih.gov/pubmed/29284181
Print-ISSN:
0934-0874
TUM Einrichtung:
Fachgebiet Nephrologie (Prof. Heemann)
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