Centre de Recherche des Cordeliers, Equipe Labellisée par la Ligue Contre le Cancer, Université de Paris Cité, Sorbonne Université, Inserm U1138, Institut Universitaire de France, 75006 Paris, France; Metabolomics and Cell Biology Platforms, Gustave Roussy Cancer Center, 94800 Villejuif, France.
Centre de Recherche des Cordeliers, Equipe Labellisée par la Ligue Contre le Cancer, Université de Paris Cité, Sorbonne Université, Inserm U1138, Institut Universitaire de France, 75006 Paris, France; Metabolomics and Cell Biology Platforms, Gustave Roussy Cancer Center, 94800 Villejuif, France; Department of Biology, Institut du Cancer Paris CARPEM, Hôpital Européen Georges Pompidou, AP-HP, 75015 Paris, France.
Semin Cell Dev Biol. 2024 Mar 15;156:11-21. doi: 10.1016/j.semcdb.2023.10.007. Epub 2023 Nov 16.
The successful treatment of oncological malignancies which results in long-term disease control or the complete eradication of cancerous cells necessitates the onset of adaptive immune responses targeting tumor-specific antigens. Such desirable anticancer immunity can be triggered via the induction of immunogenic cell death (ICD) of cancer cells, thus converting malignant cells into an in situ vaccine that elicits T cell mediated adaptive immune responses and establishes durable immunological memory. The exploration of ICD for cancer treatment has been subject to extensive research. However, functional heterogeneity among ICD activating therapies in many cases requires specific co-medications to achieve full-blown efficacy. Here, we described the hallmarks of ICD and classify ICD activators into three distinct functional categories namely, according to their mode of action: (i) ICD inducers, which increase the immunogenicity of malignant cells, (ii) ICD sensitizers, which prime cellular circuitries for ICD induction by conventional cytotoxic agents, and (iii) ICD enhancers, which improve the perception of ICD signals by antigen presenting dendritic cells. Altogether, ICD induction, sensitization and enhancement offer the possibility to convert well-established conventional anticancer therapies into immunotherapeutic approaches that activate T cell-mediated anticancer immunity.
成功治疗肿瘤恶性肿瘤需要诱导针对肿瘤特异性抗原的适应性免疫反应,从而实现长期疾病控制或完全消除癌细胞。这种理想的抗癌免疫可以通过诱导癌细胞的免疫原性细胞死亡(ICD)来触发,从而将恶性细胞转化为原位疫苗,引发 T 细胞介导的适应性免疫反应并建立持久的免疫记忆。癌症治疗中对 ICD 的探索已经受到广泛研究。然而,在许多情况下,ICD 激活治疗之间的功能异质性需要特定的联合用药才能实现完全疗效。在这里,我们描述了 ICD 的特征,并根据其作用模式将 ICD 激活剂分为三类不同的功能类别:(i)ICD 诱导剂,其增加恶性细胞的免疫原性,(ii)ICD 敏化剂,其通过常规细胞毒性药物为 ICD 诱导启动细胞通路,以及(iii)ICD 增强剂,其改善抗原呈递树突细胞对 ICD 信号的感知。总之,ICD 的诱导、敏化和增强为将成熟的常规抗癌疗法转化为激活 T 细胞介导的抗癌免疫的免疫治疗方法提供了可能性。