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231224s2017 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2016.12.003
|2 doi
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|a pubmed24n0891.xml
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|a (DE-627)NLM267486537
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|a (NLM)28025135
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|a (PII)S1521-6616(16)30197-8
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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 Zirakzadeh, A Ali
|e verfasserin
|4 aut
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|a Doxorubicin enhances the capacity of B cells to activate T cells in urothelial urinary bladder cancer
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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 05.06.2017
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|a Date Revised 03.01.2021
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2016. Published by Elsevier Inc.
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|a Cancer is currently treated by a combination of therapies, including chemotherapy which is believed to suppress the immune system. Combination of immunotherapy and chemotherapy correlates with improved survival but needs careful planning in order to achieve a synergistic effect. In this study, we have demonstrated that doxorubicin treatment of B cells resulted in increased expression of CD86 and concordantly increased CD4+ T cell activation in the presence of superantigen, an effect that was inhibited by the addition of a CD86 blocking antibody. Furthermore, doxorubicin resulted in decreased expression of the anti-inflammatory cytokines IL-10 and TNF-α. Finally, B cells from urinary bladder cancer patients, treated with a neoadjuvant regiment containing doxorubicin, displayed increased CD86-expression. We conclude that doxorubicin induces CD86 expression on B cells and hence enhances their antigen-presenting ability in vitro, a finding verified in patients. Development of tailored time and dose schedules may increase the effectiveness of combining chemotherapy and immunotherapy
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a B cells
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|a CD86
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|a Doxorubicin
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|a Immunology
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|a Neoadjuvant chemotherapy
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|a Urinary bladder cancer
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|a B7-2 Antigen
|2 NLM
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|a Tumor Necrosis Factor-alpha
|2 NLM
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|a Interleukin-10
|2 NLM
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|a 130068-27-8
|2 NLM
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|a Doxorubicin
|2 NLM
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|a 80168379AG
|2 NLM
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|a Kinn, Johan
|e verfasserin
|4 aut
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|a Krantz, David
|e verfasserin
|4 aut
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|a Rosenblatt, Robert
|e verfasserin
|4 aut
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|a Winerdal, Malin E
|e verfasserin
|4 aut
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|a Hu, Jin
|e verfasserin
|4 aut
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|a Hartana, Ciputra Adijaya
|e verfasserin
|4 aut
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|a Lundgren, Christian
|e verfasserin
|4 aut
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|a Bergman, Emma Ahlén
|e verfasserin
|4 aut
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|a Johansson, Markus
|e verfasserin
|4 aut
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|a Holmström, Benny
|e verfasserin
|4 aut
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|a Hansson, Johan
|e verfasserin
|4 aut
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|a Sidikii, Alexander
|e verfasserin
|4 aut
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|a Vasko, Janos
|e verfasserin
|4 aut
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|a Marits, Per
|e verfasserin
|4 aut
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|a Sherif, Amir
|e verfasserin
|4 aut
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|a Winqvist, Ola
|e verfasserin
|4 aut
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 176(2017) vom: 01. März, Seite 63-70
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:176
|g year:2017
|g day:01
|g month:03
|g pages:63-70
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|u http://dx.doi.org/10.1016/j.clim.2016.12.003
|3 Volltext
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|d 176
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