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Status: Bibliographieeintrag

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Verfasst von:Reichman, Avinoam [VerfasserIn]   i
 Kunz, Alexander [VerfasserIn]   i
 Joedicke, Jara Johanna [VerfasserIn]   i
 Höpken, Uta [VerfasserIn]   i
 Keib, Anna [VerfasserIn]   i
 Neuber, Brigitte [VerfasserIn]   i
 Sedloev, David [VerfasserIn]   i
 Wang, Lei [VerfasserIn]   i
 Jiang, Genqiao [VerfasserIn]   i
 Hückelhoven-Krauss, Angela [VerfasserIn]   i
 Eberhardt, Franziska [VerfasserIn]   i
 Müller-Tidow, Carsten [VerfasserIn]   i
 Wermke, Martin [VerfasserIn]   i
 Rehm, Armin [VerfasserIn]   i
 Schmitt, Michael [VerfasserIn]   i
 Schmitt, Anita [VerfasserIn]   i
Titel:Comparison of FACS and PCR for detection of BCMA-CAR-T cells
Verf.angabe:Avinoam Reichman, Alexander Kunz, Jara J. Joedicke, Uta E. Höpken, Anna Keib, Brigitte Neuber, David Sedloev, Lei Wang, Genqiao Jiang, Angela Hückelhoven-Krauss, Franziska Eberhardt, Carsten Müller-Tidow, Martin Wermke, Armin Rehm, Michael Schmitt and Anita Schmitt
E-Jahr:2022
Jahr:14 January 2022
Umfang:14 S.
Fussnoten:Gesehen am 22.03.2022
Titel Quelle:Enthalten in: International journal of molecular sciences
Ort Quelle:Basel : Molecular Diversity Preservation International, 2000
Jahr Quelle:2022
Band/Heft Quelle:23(2022), 2, Artikel-ID 903, Seite 1-14
ISSN Quelle:1422-0067
 1661-6596
Abstract:Chimeric-antigen-receptor (CAR)-T-cell therapy is already widely used to treat patients who are relapsed or refractory to chemotherapy, antibodies, or stem-cell transplantation. Multiple myeloma still constitutes an incurable disease. CAR-T-cell therapy that targets BCMA (B-cell maturation antigen) is currently revolutionizing the treatment of those patients. To monitor and improve treatment outcomes, methods to detect CAR-T cells in human peripheral blood are highly desirable. In this study, three different detection reagents for staining BCMA-CAR-T cells by flow cytometry were compared. Moreover, a quantitative polymerase chain reaction (qPCR) to detect BCMA-CAR-T cells was established. By applying a cell-titration experiment of BCMA-CAR-T cells, both methods were compared head-to-head. In flow-cytometric analysis, the detection reagents used in this study could all detect BCMA-CAR-T cells at a similar level. The results of false-positive background staining differed as follows (standard deviation): the BCMA-detection reagent used on the control revealed a background staining of 0.04% (±0.02%), for the PE-labeled human BCMA peptide it was 0.25% (±0.06%) and for the polyclonal anti-human IgG antibody it was 7.2% (±9.2%). The ability to detect BCMA-CAR-T cells down to a concentration of 0.4% was similar for qPCR and flow cytometry. The qPCR could detect even lower concentrations (0.02-0.01%). In summary, BCMA-CAR-T-cell monitoring can be reliably performed by both flow cytometry and qPCR. In flow cytometry, reagents with low background staining should be preferred.
DOI:doi:10.3390/ijms23020903
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

kostenfrei: Volltext ; Verlag: https://doi.org/10.3390/ijms23020903
 kostenfrei: Volltext: https://www.mdpi.com/1422-0067/23/2/903
 DOI: https://doi.org/10.3390/ijms23020903
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:BCMA-CAR
 detection reagent
 flow cytometry
 polymerase chain reaction
K10plus-PPN:1796018821
Verknüpfungen:→ Zeitschrift

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