RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The immune microenvironment of pathogen-associated cancers and current clinical therapeutics.
The immune microenvironment of pathogen-associated cancers and current clinical therapeutics.
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病原体相关癌症约占全球所有恶性肿瘤的15-20%,由致癌病毒、细菌和寄生虫的慢性感染引起。病原体可通过多种机制将肿瘤微环境(TME)转变为免疫抑制生态位,包括免疫检查点操控、慢性炎症、代谢重编程和直接表观遗传修饰。与癌症相关感染有关的免疫功能障碍可包括M2极化巨噬细胞、MDSCs扩增、耗竭的T/NK细胞和耐受性树突状细胞,所有这些都促进免疫逃逸和对癌症治疗的耐药性。治疗方面的进展包括预防性疫苗、免疫检查点抑制剂,以及下一代方法,如工程化沙门氏菌递送至缺氧肿瘤和靶向微生物组。病原体特异性、癌症特异性和患者特异性治疗的进步并非没有挑战,包括病原体的异质性、缺乏临床有用的生物标志物、对恢复抗病原体免疫安全性的担忧,以及多种干预措施在规模化方面的挑战。本综述将综合阐述病原体介导的TME重塑的机制方面、当代临床治疗,以及正在进行的利用病原体/宿主动力学来增强可测量的精准免疫治疗策略的研究。
Pathogen-associated cancers account roughly 15-20% of all malignancies worldwide and arise from chronic infections by oncogenic viruses, bacteria and parasites. Pathogens can alter the tumor microenvironment (TME) into an immune-suppressive niche using multiple mechanisms, including immune checkpoint manipulation, chronic inflammation, metabolic reprogramming, and direct epigenetic modifications. Immune dysfunctions related to infections linked to cancers can include M2-polarized macrophages, expansion of MDSCs, exhausted T/NK cells, and tolerogenic dendritic cells, all progressing immune evasion and resistance to cancer therapy.
Advances in therapeutics exist in prophylactic vaccines, immune checkpoint inhibitors, and next-generation methods such as the engineered Salmonella to deliver to hypoxic tumors and the targeting the microbiome. The advancement of pathogen-, cancer-, and patient-specific therapeutics is not without its challenges, including heterogeneity of the pathogens, absence of clinically useful biomarkers, concerns about the safety of the restoring anti-pathogen immunity and challenges of scale for manifold interventions.
This review will provide a synthesis of the mechanistic aspects of pathogen-mediated TME remodeling, contemporary clinical therapeutics, and ongoing investigations into using pathogen/host dynamics to enhance measurable precision immunotherapy strategies.
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