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Polymeric PD-L1 blockade nanoparticles for cancer photothermal-immunotherapy
被引:51
|作者:
Yu, Yunjian
[1
]
Li, Jie
[1
]
Song, Boyi
[1
]
Ma, Zhuang
[1
]
Zhang, Yufei
[1
]
Sun, Haonan
[1
]
Wei, Xiaosong
[1
]
Bai, Yayun
[1
]
Lu, Xueguang
[2
]
Zhang, Peng
[2
,3
]
Zhang, Xinge
[1
]
机构:
[1] Nankai Univ, Inst Polymer Chem, Coll Chem, Key Lab Funct Polymer Mat,Minist Educ, Tianjin 300071, Peoples R China
[2] MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[3] Zhejiang Univ, Dept Polymer Sci & Engn, MOE Key Lab Macromol Synth & Functionalizat, Hangzhou 310027, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
PD-L1;
blockade;
Polymeric nanoparticle;
Photothermal treatment;
Antitumor immunity;
Metastatic cancer;
IMMUNE CHECKPOINT BLOCKADE;
CALRETICULIN EXPOSURE;
CELL-DEATH;
SAFETY;
THERAPY;
COMBINATION;
ANTI-PD-1;
ANTIBODY;
D O I:
10.1016/j.biomaterials.2021.121312
中图分类号:
R318 [生物医学工程];
学科分类号:
0831 ;
摘要:
Checkpoint inhibitors, such as antibodies blocking the PD-1/PD-L1 pathway, are among the most promising immunotherapies to treat metastatic cancers, but their response rate remains low. In addition, the usage of monoclonal antibodies as checkpoint inhibitors is associated with a series of drawbacks. Herein, an all synthetic nanoparticle with PD-L1 blockade capability is developed for cancer photothermal-immunotherapy. The polymeric nanoparticle integrates photothermal treatment, antitumor vaccination, and PD-1/PD-L1 blockade in a single system to augment the antitumor efficacy. In a CT26 bilateral tumor model, intravenously injected nanoparticles accumulate in tumor sites and mediate strong photothermal effects, eradicate the NIR treated primary tumors and elicit strong antitumor immunity by inducing immunogenic cell death (ICD). Growth of the untreated distant tumors is also suppressed due to the synergies of systemic antitumor immune activation and PD-L1 blockade. Our strategy offers a simple but promising approach for the treatment of metastatic cancer.
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页数:15
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