Trial watch: chemotherapy-induced immunogenic cell death in immuno-oncology.
Isaure VanmeerbeekJenny SprootenDirk De RuysscherSabine TejparPeter VandenbergheJitka FucikovaRadek SpisekLaurence ZitvogelGuido KroemerLorenzo GalluzziAbhishek Dinkarnath GargPublished in: Oncoimmunology (2020)
The term 'immunogenic cell death' (ICD) denotes an immunologically unique type of regulated cell death that enables, rather than suppresses, T cell-driven immune responses that are specific for antigens derived from the dying cells. The ability of ICD to elicit adaptive immunity heavily relies on the immunogenicity of dying cells, implying that such cells must encode and present antigens not covered by central tolerance (antigenicity), and deliver immunostimulatory molecules such as damage-associated molecular patterns and cytokines (adjuvanticity). Moreover, the host immune system must be equipped to detect the antigenicity and adjuvanticity of dying cells. As cancer (but not normal) cells express several antigens not covered by central tolerance, they can be driven into ICD by some therapeutic agents, including (but not limited to) chemotherapeutics of the anthracycline family, oxaliplatin and bortezomib, as well as radiation therapy. In this Trial Watch, we describe current trends in the preclinical and clinical development of ICD-eliciting chemotherapy as partner for immunotherapy, with a focus on trials assessing efficacy in the context of immunomonitoring.
Keyphrases
- cell cycle arrest
- cell death
- induced apoptosis
- radiation therapy
- palliative care
- immune response
- clinical trial
- stem cells
- signaling pathway
- oxidative stress
- dendritic cells
- randomized controlled trial
- squamous cell carcinoma
- inflammatory response
- mesenchymal stem cells
- transcription factor
- study protocol
- phase ii
- chemotherapy induced
- phase iii
- open label