NIR-light-mediated spatially selective triggering of anti-tumor immunity via upconversion nanoparticle-based immunodevices

被引:168
作者
Chu, Hongqian [1 ,2 ]
Zhao, Jian [1 ,2 ]
Mi, Yongsheng [1 ,2 ]
Di, Zhenghan [1 ,2 ]
Li, Lele [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Key Lab Biomed Effects Nanomat & Nanosafety, Beijing 100190, Peoples R China
[2] Chinese Acad Sci, Ctr Excellence Nanosci, Natl Ctr Nanosci & Technol, Beijing 100190, Peoples R China
[3] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
关键词
T-CELLS; OPTOGENETICS; CPG; NANOCRYSTALS; STIMULATION; INHIBITION; ACTIVATION; CIRCUITS; DELIVERY; AGONISTS;
D O I
10.1038/s41467-019-10847-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Immunomodulatory therapies are becoming a paradigm-shifting treatment modality for cancer. Despite promising clinical results, cancer immunotherapy is accompanied with offtumor toxicity and autoimmune adverse effects. Thus, the development of smarter systems to regulate immune responses with superior spatiotemporal precision and enhanced safety is urgently needed. Here we report an activatable engineered immunodevice that enables remote control over the antitumor immunity in vitro and in vivo with near-infrared (NIR) light. The immunodevice is composed of a rationally designed UV light-activatable immunostimulatory agent and upconversion nanoparticle, which acts as a transducer to shift the light sensitivity of the device to the NIR window. The controlled immune regulation allows the generation of effective immune response within tumor without disturbing immunity elsewhere in the body, thereby maintaining the antitumor efficacy while mitigating systemic toxicity. The present work illustrates the potential of the remote-controlled immunodevice for triggering of immunoactivity at the right time and site.
引用
收藏
页数:11
相关论文
共 61 条
[1]
Adamus Tomasz, 2018, Contemp Oncol (Pozn), V22, P56, DOI 10.5114/wo.2018.73887
[2]
GFP-specific CD8 T cells enable targeted cell depletion and visualization of T-cell interactions [J].
Agudo, Judith ;
Ruzo, Albert ;
Park, Eun Sook ;
Sweeney, Robert ;
Kana, Veronika ;
Wu, Meng ;
Zhao, Yong ;
Egli, Dieter ;
Merad, Miriam ;
Brown, Brian D. .
NATURE BIOTECHNOLOGY, 2015, 33 (12) :1287-+
[3]
Optochemical Control of Biological Processes in Cells and Animals [J].
Ankenbruck, Nicholas ;
Courtney, Taylor ;
Naro, Yuta ;
Deiters, Alexander .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 57 (11) :2768-2798
[4]
Upconversion and anti-stokes processes with f and d ions in solids [J].
Auzel, F .
CHEMICAL REVIEWS, 2004, 104 (01) :139-173
[5]
Baines J, 2003, CLIN CANCER RES, V9, P2693
[6]
The Extent of Irradiation-Induced Long-Term Visceral Organ Damage Depends on Cranial/Brain Exposure [J].
Boittin, Francois-Xavier ;
Denis, Josiane ;
Mayol, Jean-Francois ;
Martigne, Patrick ;
Raffin, Florent ;
Coulon, David ;
Grenier, Nancy ;
Drouet, Michel ;
Herodin, Francis .
PLOS ONE, 2015, 10 (04)
[7]
Light-Controlled Tools [J].
Brieke, Clara ;
Rohrbach, Falk ;
Gottschalk, Alexander ;
Mayer, Guenter ;
Heckel, Alexander .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2012, 51 (34) :8446-8476
[8]
A Roadmap to Success in Photopharmacology [J].
Broichhagen, Johannes ;
Frank, James Allen ;
Trauner, Dirk .
ACCOUNTS OF CHEMICAL RESEARCH, 2015, 48 (07) :1947-1960
[9]
Optogenetic protein clustering and signaling activation in mammalian cells [J].
Bugaj, Lukasz J. ;
Choksi, Atri T. ;
Mesuda, Colin K. ;
Kane, Ravi S. ;
Schaffer, David V. .
NATURE METHODS, 2013, 10 (03) :249-252
[10]
Oncology Meets Immunology: The Cancer-Immunity Cycle [J].
Chen, Daniel S. ;
Mellman, Ira .
IMMUNITY, 2013, 39 (01) :1-10