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
相关论文
共 50 条
  • [1] Immune Checkpoint Blockade in Combination with Stereotactic Body Radiotherapy in Patients with Metastatic Pancreatic Ductal Adenocarcinoma
    Xie, Changqing
    Duffy, Austin G.
    Brar, Gagandeep
    Fioravanti, Suzanne
    Mabry-Hrones, Donna
    Walker, Melissa
    Bonilla, Cecilia Monge
    Wood, Bradford J.
    Citrin, Deborah E.
    Ramirez, Elizabeth M. Gil
    Escorcia, Freddy E.
    Redd, Bernadette
    Hernandez, Jonathan M.
    Davis, Jeremy L.
    Gasmi, Billel
    Kleiner, David
    Steinberg, Seth M.
    Jones, Jennifer C.
    Greten, Tim F.
    CLINICAL CANCER RESEARCH, 2020, 26 (10) : 2318 - 2326
  • [2] The Immune Checkpoint Landscape in Tumor Cells of Pancreatic Ductal Adenocarcinoma
    Loch, Florian N. N.
    Kamphues, Carsten
    Beyer, Katharina
    Schineis, Christian
    Rayya, Wael
    Lauscher, Johannes C. C.
    Horst, David
    Dragomir, Mihnea P. P.
    Schallenberg, Simon
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (03)
  • [3] Hypoxia and pancreatic ductal adenocarcinoma
    Yamasaki, Akio
    Yanai, Kosuke
    Onishi, Hideya
    CANCER LETTERS, 2020, 484 : 9 - 15
  • [4] PSGL-1-deficiency promotes pancreatic ductal adenocarcinoma tumor control and synergy with immune checkpoint blockade
    Hope, Jennifer L.
    Zhang, Yijuan
    Faso, Hannah A.
    Roy, Sreeja
    Lin, Michelle
    Palete, Ashley B.
    Maganti, Swetha
    Otero, Dennis C.
    Commisso, Cosimo
    Bradley, Linda M.
    CANCER RESEARCH, 2024, 84 (02)
  • [5] Major hurdles of immune-checkpoint inhibitors in pancreatic ductal adenocarcinoma
    Akhuba, Liia
    Tigai, Zhanna
    Shek, Dmitrii
    CANCER DRUG RESISTANCE, 2023, 6 (02) : 327 - 331
  • [6] ERK Inhibition Improves Anti-PD-L1 Immune Checkpoint Blockade in Preclinical Pancreatic Ductal Adenocarcinoma
    Henry, Kelly E.
    Mack, Kyeara N.
    Nagle, Veronica L.
    Cornejo, Mike
    Michel, Adam O.
    Fox, Ian L.
    Davydova, Maria
    Dilling, Thomas R.
    Pillarsetty, Nagavarakishore
    Lewis, Jason S.
    MOLECULAR CANCER THERAPEUTICS, 2021, 20 (10) : 2026 - 2034
  • [7] Oxygen metabolism and hypoxia tolerance in organoid models of pancreatic ductal adenocarcinoma
    Zhang, Ji
    Liu, Qingquan
    Cojocari, Dan
    Zaidi, Mark
    McKee, Trevor
    Radulovich, Nikolina
    Tsao, Ming-Sound
    Hedley, David
    Koritzinsky, Marianne
    Wouters, Bradly G.
    CANCER RESEARCH, 2018, 78 (13)
  • [8] Vasoactive intestinal peptide signaling - a novel immune checkpoint in pancreatic ductal adenocarcinoma
    Ravindranathan, Sruthi
    Li, Yiwen
    Wang, Shuhua
    Zaidi, Mohammad
    Lesinski, Gregory B.
    El-Rayes, Bassel
    Waller, Edmund K.
    JOURNAL OF IMMUNOLOGY, 2019, 202 (01):
  • [9] Immune Checkpoint Inhibition for Pancreatic Ductal Adenocarcinoma: Current Limitations and Future Options
    Kabacaoglu, Derya
    Ciecielski, Katrin J.
    Ruess, Dietrich A.
    Alguel, Hana
    FRONTIERS IN IMMUNOLOGY, 2018, 9
  • [10] Analysis of a novel immune checkpoint, Siglec-15, in pancreatic ductal adenocarcinoma
    Chen, Xianlong
    Mo, Shengwei
    Zhang, Yue
    Ma, Heng
    Lu, Zhaohui
    Yu, Shuangni
    Chen, Jie
    JOURNAL OF PATHOLOGY CLINICAL RESEARCH, 2022, 8 (03): : 268 - 278