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231224s2017 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2017.04.016
|2 doi
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|a pubmed24n0904.xml
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|a (NLM)28461110
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|a (PII)S1521-6616(17)30161-4
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Zhu, Jiqiao
|e verfasserin
|4 aut
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|a Granzyme B producing B-cells in renal transplant patients
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|c 2017
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 16.11.2017
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|a Date Revised 02.12.2018
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2017 Elsevier Inc. All rights reserved.
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|a 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)
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|a 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
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|a 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
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|a 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
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|a Journal Article
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|a Allograft rejection
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|a B-cells
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|a Immune tolerance
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|a Regulatory B-cells
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|a Renal transplantation
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|a Adrenal Cortex Hormones
|2 NLM
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|a Immunosuppressive Agents
|2 NLM
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|a Interleukins
|2 NLM
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|a Cyclosporine
|2 NLM
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|a 83HN0GTJ6D
|2 NLM
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|a GZMB protein, human
|2 NLM
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|a EC 3.4.21.-
|2 NLM
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|a Granzymes
|2 NLM
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|a EC 3.4.21.-
|2 NLM
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|a Mycophenolic Acid
|2 NLM
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|a HU9DX48N0T
|2 NLM
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|a interleukin-21
|2 NLM
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|a MKM3CA6LT1
|2 NLM
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|a Tacrolimus
|2 NLM
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|a WM0HAQ4WNM
|2 NLM
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|a Zeng, Ye
|e verfasserin
|4 aut
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|a Dolff, Sebastian
|e verfasserin
|4 aut
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|a Bienholz, Anja
|e verfasserin
|4 aut
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|a Lindemann, Monika
|e verfasserin
|4 aut
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|a Brinkhoff, Alexandra
|e verfasserin
|4 aut
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|a Schedlowski, Manfred
|e verfasserin
|4 aut
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|a Xu, Shilei
|e verfasserin
|4 aut
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|a Sun, Ming
|e verfasserin
|4 aut
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|a Guberina, Hana
|e verfasserin
|4 aut
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|a Kirchhof, Julia
|e verfasserin
|4 aut
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|a Kribben, Andreas
|e verfasserin
|4 aut
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|a Witzke, Oliver
|e verfasserin
|4 aut
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|a Wilde, Benjamin
|e verfasserin
|4 aut
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 184(2017) vom: 10. Nov., Seite 48-53
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:184
|g year:2017
|g day:10
|g month:11
|g pages:48-53
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|u http://dx.doi.org/10.1016/j.clim.2017.04.016
|3 Volltext
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|d 184
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