Granzyme B producing B-cells in renal transplant patients

Copyright © 2017 Elsevier Inc. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 184(2017) vom: 10. Nov., Seite 48-53
1. Verfasser: Zhu, Jiqiao (VerfasserIn)
Weitere Verfasser: Zeng, Ye, Dolff, Sebastian, Bienholz, Anja, Lindemann, Monika, Brinkhoff, Alexandra, Schedlowski, Manfred, Xu, Shilei, Sun, Ming, Guberina, Hana, Kirchhof, Julia, Kribben, Andreas, Witzke, Oliver, Wilde, Benjamin
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2017
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Allograft rejection B-cells Immune tolerance Regulatory B-cells Renal transplantation Adrenal Cortex Hormones Immunosuppressive Agents Interleukins Cyclosporine mehr... 83HN0GTJ6D GZMB protein, human EC 3.4.21.- Granzymes Mycophenolic Acid HU9DX48N0T interleukin-21 MKM3CA6LT1 Tacrolimus WM0HAQ4WNM
Beschreibung
Zusammenfassung:Copyright © 2017 Elsevier Inc. All rights reserved.
OBJECTIVES: A separate subset of Granzyme B (GrB) producing B-cells regulating T-cell mediated immunity has been identified. In the present study, we investigated the role of GrB+ B-cells in renal transplant patients (RTX)
METHODS: 12 healthy controls (HC) and 26 RTX patients were enrolled. In addition, 19 healthy volunteers treated with cyclosporine A (CsA) were enrolled. GrB+ B-cells were determined via flow cytometry
RESULTS: RTX Patients showed a diminished fraction of GrB+ B-cells as compared to HC. CsA treatment of healthy volunteers had no impact on the development of GrB+ B-cells. RTX patients with a history of allograft rejection showed an increased frequency of GrB+ B-cells. RTX patients with at least one episode of CMV viremia tended to have lower GrB+ B-cells as compared to patients without viremic episodes
CONCLUSION: We demonstrate that treatment with CsA does not impair the development of GrB+ B-cells. GrB+ B-cells may have a dual role in renal transplantation as regulatory cells to maintain allospecific tolerance and as effector cells enhancing viral control
Beschreibung:Date Completed 16.11.2017
Date Revised 02.12.2018
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-7035
DOI:10.1016/j.clim.2017.04.016