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:Recombinant Strains of Oncolytic Vaccinia Virus for Cancer Immunotherapy.
Recombinant Strains of Oncolytic Vaccinia Virus for Cancer Immunotherapy.
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癌症病毒治疗是一种基于选择性感染并杀死肿瘤细胞的病毒的替代性治疗方法。痘苗病毒(VV)是痘病毒科的成员,该科为有包膜病毒家族,具有大型线性双链DNA基因组。VV毒株已被证实的安全性以及病毒基因组相当大的转基因容量,使VV成为构建用于癌症治疗的重组溶瘤病毒的优良平台。此外,多种遗传修饰可通过将免疫调节基因或促凋亡分子武装到VV中、增强宿主免疫系统以及增加T细胞或NK细胞对肿瘤细胞的交叉致敏识别,从而提高VV的肿瘤选择性和治疗效果。在本综述中,我们总结了通过生物工程方法开发用于增强癌症免疫治疗的重组VV毒株的相关数据。
Cancer virotherapy is an alternative therapeutic approach based on the viruses that selectively infect and kill tumor cells. Vaccinia virus (VV) is a member of the Poxviridae, a family of enveloped viruses with a large linear double-stranded DNA genome. The proven safety of the VV strains as well as considerable transgene capacity of the viral genome, make VV an excellent platform for creating recombinant oncolytic viruses for cancer therapy.
Furthermore, various genetic modifications can increase tumor selectivity and therapeutic efficacy of VV by arming it with the immune-modulatory genes or proapoptotic molecules, boosting the host immune system, and increasing cross-priming recognition of the tumor cells by T-cells or NK cells. In this review, we summarized the data on bioengineering approaches to develop recombinant VV strains for enhanced cancer immunotherapy.
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