Near-Infrared Nano-Optogenetic Activation of Cancer Immunotherapy via Engineered Bacteria.
Xiaoqiang ZhuSihan ChenXiuwen HuLijun ZhaoYiqian WangJinzhao HuangJiawen ChenYuzhi QiuXuefei ZhangMengdie WangXiangliang YangYan ZhangYanhong ZhuPublished in: Advanced materials (Deerfield Beach, Fla.) (2022)
Certain anaerobic microbes with the capability to colonize in tumor microenvironment tend to express the heterologous gene in a sustainable manner, which would inevitably comprise the therapeutic efficacy and induce off-tumor toxicity in vivo. To improve the therapeutic precision and controllability of bacteria-based therapeutics, Escherichia coli Nissle 1917 (EcN) engineered to sense blue light and release the encoded flagellin B (flaB), is conjugated with lanthanide upconversion nanoparticles (UCNPs) for near-infrared (NIR) nano-optogenetic cancer immunotherapy. Upon 808 nm photoirradiation, UCNPs emit at the blue region to photoactivate the EcN for secretion of flaB, which subsequently binds to Toll-like receptor 5 expressed on the membrane of macrophages for activating immune response via MyD88-dependent signal pathway. Such synergism leads to significant tumor regression in different tumor models and metastatic tumors with negligible side effects. Our studies based on NIR nano-optogenetic platform highlight the rational of leveraging the optogenetic tools combined natural propensity of certain bacteria for cancer immunotherapy. This article is protected by copyright. All rights reserved.
Keyphrases
- toll like receptor
- photodynamic therapy
- immune response
- escherichia coli
- nuclear factor
- inflammatory response
- small cell lung cancer
- signaling pathway
- small molecule
- microbial community
- fluorescence imaging
- dendritic cells
- genome wide
- oxidative stress
- copy number
- dna methylation
- gene expression
- high throughput
- staphylococcus aureus
- pseudomonas aeruginosa
- biofilm formation
- multidrug resistant
- genome wide analysis