Fidelle Marine, Yonekura Satoru, Picard Marion, Cogdill Alexandria, Hollebecque Antoine, Roberti Maria Paula, Zitvogel Laurence
Gustave Roussy, Villejuif, France.
Institut National de la Santé Et de la Recherche Médicale (INSERM) U1015, Villejuif, France.
Front Immunol. 2020 Dec 14;11:600886. doi: 10.3389/fimmu.2020.600886. eCollection 2020.
While colorectal cancers (CRC) are paradigmatic tumors invaded by effector memory lymphocytes, the mechanisms accounting for the relative resistance of MSI negative CRC to immunogenic cell death mediated by oxaliplatin and immune checkpoint inhibitors has remained an open conundrum. Here, we propose the viewpoint where its microenvironmental contexture could be explained -at least in part- by macroenvironmental cues constituted by the complex interplay between the epithelial barrier, its microbial ecosystem, and the local immune system. Taken together this dynamic ménage-à-trois offers novel coordinated actors of the humoral and cellular immune responses actionable to restore sensitivity to immune checkpoint inhibition. Solving this paradox involves breaking tolerance to crypt stem cells by inducing the immunogenic apoptosis of ileal cells in the context of an ileal microbiome shifted towards immunogenic bacteria using cytotoxicants. This manoeuver results in the elicitation of a productive Tfh and B cell dialogue in mesenteric lymph nodes culminating in tumor-specific memory CD8 T cell responses sparing the normal epithelium.
虽然结直肠癌(CRC)是效应记忆淋巴细胞浸润的典型肿瘤,但MSI阴性CRC对奥沙利铂和免疫检查点抑制剂介导的免疫原性细胞死亡具有相对抗性的机制仍是一个未解之谜。在此,我们提出一种观点,即其微环境结构至少部分可以由上皮屏障、其微生物生态系统和局部免疫系统之间复杂相互作用所构成的宏观环境线索来解释。这一动态的三方组合提供了体液和细胞免疫反应的新型协同作用因子,可用于恢复对免疫检查点抑制的敏感性。解决这一矛盾需要在使用细胞毒性药物使回肠微生物群向免疫原性细菌转变的背景下,通过诱导回肠细胞的免疫原性凋亡来打破对隐窝干细胞的耐受性。这一策略导致在肠系膜淋巴结中引发有效的滤泡辅助性T细胞(Tfh)和B细胞对话,最终产生肿瘤特异性记忆CD8 T细胞反应,同时保护正常上皮。