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氨基双膦酸盐作为基于γδT细胞的癌症免疫疗法的新武器。

Aminobisphosphonates as new weapons for gammadelta T Cell-based immunotherapy of cancer.

作者信息

Caccamo Nadia, Meraviglia Serena, Cicero Giuseppe, Gulotta Gaspare, Moschella Francesco, Cordova Adriana, Gulotta Eliana, Salerno Alfredo, Dieli Francesco

机构信息

Dipartimento di Biopatologia e Metodologie Biomediche, Università di Palermo, Corso Tukory 211, Palermo 90134 Italy.

出版信息

Curr Med Chem. 2008;15(12):1147-53. doi: 10.2174/092986708784310468.

Abstract

Several observations in mice and in humans have collectively laid the foundation for examining the potential of gammadelta T cells to exert tumor immunotherapy. Human gammaDelta T cells can be activated in a non-MHC dependent fashion either by low molecular mass phosphoantigens, or by agents that provoke the accumulation of endogenous pyrophosphates such as isopentenylpyrophosphate. Among the latter, aminobisphosphonates are well-established in the clinic, and extensive data are available on the compounds' antiangiogenic, antiosteolytic and pro-apoptotic properties. In this review we discuss on the possibility that the intentional activation of gammadelta T cells in vivo by aminobisphosphonates may represent a promising target for the design of novel and highly innovative immunotherapy in patients with different types of cancer.

摘要

在小鼠和人类中的多项观察结果共同为研究γδ T细胞发挥肿瘤免疫治疗的潜力奠定了基础。人类γδ T细胞可以通过低分子量磷酸抗原来以非MHC依赖的方式被激活,或者通过引发内源性焦磷酸盐积累的物质(如异戊烯基焦磷酸)来激活。在后者中,氨基双膦酸盐在临床上已得到充分证实,并且关于这些化合物的抗血管生成、抗骨溶解和促凋亡特性有大量数据。在本综述中,我们讨论了氨基双膦酸盐在体内有意激活γδ T细胞可能成为为不同类型癌症患者设计新型和高度创新免疫疗法的一个有前景靶点的可能性。

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