免疫原性细胞死亡
医学
阿霉素
米托蒽醌
心脏毒性
硼替佐米
表阿霉素
程序性细胞死亡
药理学
化疗
免疫系统
癌症研究
环磷酰胺
免疫学
细胞凋亡
免疫疗法
内科学
生物
多发性骨髓瘤
生物化学
作者
Jonathan Pol,Erika Vacchelli,Fernando Aranda,Francesca Castoldi,Alexander Eggermont,Isabelle Cremer,Catherine Sautès‐Fridman,Jitka Fučíková,Jérôme Galon,Radek Špíšek,Éric Tartour,Laurence Zitvogel,Guido Kroemer,Lorenzo Galluzzi
出处
期刊:OncoImmunology
[Landes Bioscience]
日期:2015-03-02
卷期号:4 (4): e1008866-e1008866
被引量:289
标识
DOI:10.1080/2162402x.2015.1008866
摘要
The term "immunogenic cell death" (ICD) is now employed to indicate a functionally peculiar form of apoptosis that is sufficient for immunocompetent hosts to mount an adaptive immune response against dead cell-associated antigens. Several drugs have been ascribed with the ability to provoke ICD when employed as standalone therapeutic interventions. These include various chemotherapeutics routinely employed in the clinic (e.g., doxorubicin, epirubicin, idarubicin, mitoxantrone, bleomycin, bortezomib, cyclophosphamide and oxaliplatin) as well as some anticancer agents that are still under preclinical or clinical development (e.g., some microtubular inhibitors of the epothilone family). In addition, a few drugs are able to convert otherwise non-immunogenic instances of cell death into bona fide ICD, and may therefore be employed as chemotherapeutic adjuvants within combinatorial regimens. This is the case of cardiac glycosides, like digoxin and digitoxin, and zoledronic acid. Here, we discuss recent developments on anticancer chemotherapy based on ICD inducers.
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