Injectable cold atmospheric plasma-activated immunotherapeutic hydrogel for enhanced cancer treatment

被引:31
|
作者
Fang, Tianxu [1 ,2 ]
Cao, Xiaona [1 ,2 ,3 ]
Shen, Bingzheng [1 ,2 ]
Chen, Zhitong [4 ,5 ]
Chen, Guojun [1 ,2 ]
机构
[1] McGill Univ, Dept Biomed Engn, Montreal, PQ H3G 0B1, Canada
[2] McGill Univ, Rosalind & Morris Goodman Canc Inst, Montreal, PQ H3G 0B1, Canada
[3] Tianjin Med Univ, Sch Nursing, Tianjin, Peoples R China
[4] Chinese Acad Sci, Inst Biomed & Hlth Engn, Shenzhen Inst Adv Technol, Shenzhen 518055, Peoples R China
[5] Natl Innovat Ctr Adv Med Devices, Ctr Adv Therapy, Shenzhen, Peoples R China
关键词
Immune checkpoint blockade; Cold atmospheric plasma; Injectable hydrogel; Cancer immunotherapy; Drug delivery; IMMUNE-CHECKPOINT BLOCKADE; IMMUNOGENIC CELL-DEATH; OXIDATIVE DNA-DAMAGE; MECHANISMS; CYTOTOXICITY; COMBINATION; ROS;
D O I
10.1016/j.biomaterials.2023.122189
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Despite the promise of immune checkpoint blockade (ICB) for cancer treatment, challenges associated with this therapy still exist, including low response rates and severe side effects in patients. Here, we report a hydrogelmediated combination therapy for enhanced ICB therapy. Specifically, cold atmospheric plasma (CAP), an ionized gas consisting of therapeutically effective reactive oxygen species (ROS) and reactive nitrogen species (RNS), can effectively induce cancer immunogenic cell death, releasing tumor-associated antigens in situ and initiating anti-tumor immune responses, which, therefore, can synergistically augment the efficacy of immune checkpoint inhibitors. To minimize the systemic toxicity of immune checkpoint inhibitors and improve the tissue penetration of CAP, an injectable Pluronic hydrogel was employed as a delivery method. Our results show that major long-lived ROS and RNS in CAP can be effectively persevered in Pluronic hydrogel and remain efficacious in inducing cancer immunogenic cell death after intratumoral injection. Our findings suggest that local hydrogelmediated combination of CAP and ICB treatment can evoke both strong innate and adaptive, local and systemic anti-tumor immune responses, thereby inhibiting both tumor growth and potential metastatic spread.
引用
收藏
页数:11
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