免疫疗法
免疫系统
RNA干扰
核糖核酸
生物
免疫学
医学
计算生物学
癌症研究
生物化学
基因
作者
Masuma Akter Monty,Md. Ariful Islam,Nan Xu,Jingwen Tan,Israth Jahan Tuhin,Xiaowen Tang,Miao Miao,Depei Wu,Lei Yu
摘要
RNAi effectors (e.g. siRNA, shRNA and miRNA) can trigger the silencing of specific genes causing alteration of genomic functions becoming a new therapeutic area for the treatment of infectious diseases, neurodegenerative disorders and cancer. In cancer treatment, RNAi effectors showed potential immunomodulatory actions by down‐regulating immuno‐suppressive proteins, such as PD‐1 and CTLA‐4, which restrict immune cell function and present challenges in cancer immunotherapy. Therefore, compared with extracellular targeting by antibodies, RNAi‐mediated cell‐intrinsic disruption of inhibitory pathways in immune cells could promote an increased anti‐tumour immune response. Along with non‐viral vectors, DNA‐based RNAi strategies might be a more promising method for immunomodulation to silence multiple inhibitory pathways in T cells than immune checkpoint blockade antibodies. Thus, in this review, we discuss diverse RNAi implementation strategies, with recent viral and non‐viral mediated RNAi synergism to immunotherapy that augments the anti‐tumour immunity. Finally, we provide the current progress of RNAi in clinical pipeline.
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