Oxygen microcapsules improve immune checkpoint blockade by ameliorating hypoxia condition in pancreatic ductal adenocarcinoma

被引:19
|
作者
Wu, Jiangchao [1 ,2 ,3 ]
Wang, Xun [1 ,2 ,3 ]
Chen, Li [4 ,5 ,6 ]
Wang, Jianing [1 ,2 ,3 ]
Zhang, Junlei [1 ,2 ,3 ]
Tang, Jianghui [1 ,2 ,3 ]
Ji, Yongtao [1 ,2 ,3 ]
Song, Jinyuan [1 ,2 ,3 ]
Wang, Lin [1 ,2 ,3 ]
Zhao, Yaxing [1 ,2 ,3 ]
Zhang, Hui [1 ,2 ,3 ]
Li, Taohong [1 ,2 ,3 ]
Sheng, Jianpeng [1 ,2 ,3 ]
Chen, Dong [4 ,5 ,6 ]
Zhang, Qi [1 ,2 ,3 ]
Liang, Tingbo [1 ,2 ,3 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 1, Dept Hepatobiliary & Pancreat Surg, Sch Med, Hangzhou 310003, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 1, Zhejiang Prov Key Lab Pancreat Dis, Sch Med, Hangzhou 310003, Peoples R China
[3] Zhejiang Univ, Canc Ctr, Hangzhou 310003, Peoples R China
[4] Zhejiang Univ, Affiliated Hosp 1, Sch Med, Dept Med Oncol, 79 Qingchun Rd, Hangzhou 310003, Zhejiang, Peoples R China
[5] Zhejiang Univ, Coll Energy Engn, Hangzhou 310027, Peoples R China
[6] Zhejiang Univ, State Key Lab Fluid Power & Mechatron Syst, Hangzhou 310027, Peoples R China
基金
中国国家自然科学基金;
关键词
Hypoxia; PD-1; Tumor microenvironment; Pancreatic ductal adenocarcinoma; Oxygen microcapsules; PHOTODYNAMIC THERAPY; CANCER; CELLS; MICROENVIRONMENT; IMMUNOTHERAPY; NANOPARTICLES;
D O I
10.1016/j.bioactmat.2022.05.022
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Rationale: Hypoxia in tumor microenvironment (TME) represents an obstacle to the efficacy of immunotherapy for pancreatic ductal adenocarcinoma (PDAC) through several aspects such as increasing the expression of immune checkpoints or promoting fibrosis. Reversing hypoxic TME is a potential strategy to improve the validity of immune checkpoint blockade (ICB). Methods: Here, we synthesized polydopamine-nanoparticle-stabilized oxygen microcapsules with excellent stabilization, bioavailability, and biocompatibility for direct oxygen delivery into tumor sites by interfacial polymerization. Results: We observed oxygen microcapsules enhanced the oxygen concentration in the hypoxia environment and maintained the oxygen concentration for a long period both in vitro and in vivo. We found that oxygen micro capsules could significantly improve the efficiency of ICB against PDAC in vivo. Mechanismly, combined treatments using oxygen microcapsules and ICB could reduce the infiltration of tumor-associated macrophages (TAMs) and polarized pro-tumor M2 macrophages into anti-tumor M1 macrophages. In addition, combined treatments could elevate the proportion of T helper subtype 1 cells (Th1 cells) and cytotoxic T lymphocytes cells (CTLs) to mediate anti-tumor immune response in TME. Conclusion: In summary, this pre-clinical study indicated that reversing hypoxia in TME by using oxygen microcapsules was an effective strategy to improve the performances of ICB on PDAC, which holds great potential for treating PDAC in the future.
引用
收藏
页码:259 / 270
页数:12
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