Adaptive Immune Response to and Survival Effect of Temozolomide- and Valproic Acid-induced Autophagy in Glioblastoma

被引:0
作者
Proske, Judith [1 ,2 ]
Walter, Lisa [3 ]
Bumes, Elisabeth [1 ,2 ]
Hutterer, Markus [1 ,2 ]
Vollmann-Zwerenz, Arabel [1 ,2 ]
Eyuepoglu, Ilker Y. [4 ]
Savaskan, Nicolai E. [4 ]
Seliger, Corinna [1 ,2 ]
Hau, Peter [1 ,2 ]
Uhl, Martin [5 ]
机构
[1] Univ Regensburg, Sch Med, Dept Neurosurg, D-93053 Regensburg, Germany
[2] Univ Regensburg, Sch Med, Wilhelm Sander NeuroOncol Unit, D-93053 Regensburg, Germany
[3] Univ Erlangen Nurnberg, Univ Hosp, Dept Dermatol, D-91054 Erlangen, Germany
[4] Univ Erlangen Nurnberg, Univ Hosp, Dept Neurosurg, D-91054 Erlangen, Germany
[5] Univ Erlangen Nurnberg, Univ Hosp, Dept Neurol, Schwabachanlage 6, D-91054 Erlangen, Germany
关键词
Temozolomide; valproic acid; autophagy; glioblastoma; dendritic cells; CD8; T-cells; CD8(+) T-CELLS; ADJUVANT TEMOZOLOMIDE; GLIOMA-CELLS; TRIAL; CHEMOTHERAPY; DEATH; RADIOTHERAPY; CONCOMITANT; MULTIFORME; RADIATION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: The combination of radiotherapy, temozolomide and valproic acid (VPA) has shown some promise in retrospective analyses of patients with glioblastoma, although their mechanisms of action remain unknown. Materials and Methods: We investigated the in vitro and in vivo effects of pretreating glioma cells with temozolomide and VPA as an immunization strategy to boost an adaptive immune response in a syngeneic mouse model. Results: Temozolomide and VPA induced autophagy in GL261 glioma cells, and caused tumor antigen-specific T-cells to become activated effector T-cells. Mice with a pre-existing glioma showed no improvement in clinical outcome when immunized with temozolomide-and VPA-treated glioma cells. Conclusion: Although temozolomide and VPA treatment of glioma cells can boost the adaptive immune response, in the context of a vaccine therapy, additional factors are necessary to eradicate the tumor and improve survival.
引用
收藏
页码:899 / 905
页数:7
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