| Literature DB >> 28025135 |
A Ali Zirakzadeh1, Johan Kinn1, David Krantz1, Robert Rosenblatt2, Malin E Winerdal1, Jin Hu1, Ciputra Adijaya Hartana1, Christian Lundgren1, Emma Ahlén Bergman1, Markus Johansson3, Benny Holmström4, Johan Hansson5, Alexander Sidikii6, Janos Vasko7, Per Marits1, Amir Sherif8, Ola Winqvist9.
Abstract
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.Entities:
Keywords: B cells; CD86; Doxorubicin; Immunology; Neoadjuvant chemotherapy; Urinary bladder cancer
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Year: 2016 PMID: 28025135 DOI: 10.1016/j.clim.2016.12.003
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969