Synergizing immunotherapy with molecular-targeted anticancer treatment

被引:5
作者
Fernandez, Ariel [1 ,2 ,3 ]
机构
[1] CNR, CONICET, Inst Argentino Matemat, RA-1083 Buenos Aires, DF, Argentina
[2] Collegium Basilea, Inst Adv Study, CH-4053 Basel, Switzerland
[3] Ariel Fernandez Consultancy, RA-1112 Buenos Aires, DF, Argentina
关键词
KINASE INHIBITOR; DASATINIB; IMATINIB; CANCER; ACTIVATION; GROWTH; CELLS;
D O I
10.1016/j.drudis.2014.03.022
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The therapeutic opportunity for anticancer kinase inhibitors (KIs) that block cell-signaling pathways is materializing. Yet, these molecular-targeted therapies are not tailored to be allies of the immune system, and often antagonize it despite generating antigenic activity. KIs usually offer an incomplete cure and one culprit is the lack of synergy between the drug and the immune system, a problem that is magnified when the therapeutic context involves HIV-1-induced immunosuppression (AIDS). We outline a strategy to fulfill the therapeutic imperative of recruiting cooperative immune responses. Accordingly, we propose a method to redesign anticancer drugs to harness the antigenic products of drug-induced apoptosis of tumor cells, thus eliciting an adjuvant immune response.
引用
收藏
页码:1427 / 1432
页数:6
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