PD-1 blockade augments CD8+T cell dependent antitumor immunity triggered by Ad-SGE-REIC in Egfr-mutant lung cancer

被引:0
作者
Nakasuka, Takamasa [1 ]
Ohashi, Kadoaki [2 ,7 ]
Nishii, Kazuya [1 ]
Hirabae, Atsuko [1 ]
Okawa, Sachi [1 ]
Tomonobu, Nahoko [3 ]
Takada, Kenji [1 ]
Ando, Chihiro [1 ]
Watanabe, Hiromi [2 ]
Makimoto, Go [2 ]
Ninomiya, Kiichiro [1 ]
Fujii, Masanori [2 ]
Kubo, Toshio [4 ]
Ichihara, Eiki [2 ]
Hotta, Katsuyuki [5 ]
Tabata, Masahiro [4 ]
Kumon, Hiromi [6 ]
Maeda, Yoshinobu [1 ]
Kiura, Katsuyuki [2 ]
机构
[1] Okayama Univ, Grad Sch Med, Dept Hematol Oncol & Resp Med, Dent & Pharmaceut Sci, Okayama, Japan
[2] Okayama Univ Hosp, Dept Resp Med, Okayama, Japan
[3] Okayama Univ, Grad Sch Med, Dept Cell Biol, Dent & Pharmaceut Sci, Okayama, Japan
[4] Okayama Univ Hosp, Ctr Clin Oncol, Okayama, Japan
[5] Okayama Univ Hosp, Ctr Innovat Clin Med, Okayama, Japan
[6] Okayama Univ, Innovat Ctr Okayama Nanobio targeted Therapy, Okayama, Japan
[7] Okayama Univ Hosp, Dept Resp Med, 2-5-1 Shikata cho,Kita ku, Okayama 7008558, Japan
关键词
EGFR mutation; Non-small cell lung cancer; Antitumor immunity; Non-inflamed tumor; Ad-SGE-REIC; Gene therapy; PD-1; CHECKPOINT INHIBITORS; PROSTATE-CANCER; DOWN-REGULATION; REIC/DKK-3; ACTIVATION; EXPRESSION; MUTATIONS; TRIAL;
D O I
10.1016/j.lungcan.2023.01.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: No immunotherapeutic protocol has yet been established in never-smoking patients with lung cancer harboring driver oncogenic mutations, such as epidermal growth factor receptor (EGFR) mutations. The immunostimulatory effect of Ad-REIC, a genetically engineered adenovirus vector expressing a tumor suppressor gene, reduced expression in immortalized cells (REIC), has been investigated in clinical trials for various solid tumors. However, the immunostimulatory effect of the Ad-REIC in EGFR-mutant lung cancer with a non-inflamed tumor microenvironment (TME) has not been explored. Materials and methods: We used a syngeneic mouse model developed by transplanting Egfr-mutant lung cancer cells into single or double flanks of C57BL/6J mice. Ad-SGE-REIC, a 2nd-generation vector with an enhancer sequence, was injected only into the tumors from one flank, and its antitumor effects were assessed. Tumor -infiltrating cells were evaluated using immunohistochemistry or flow cytometry. The synergistic effects of Ad-SGE-REIC and PD-1 blockade were also examined. Results: Injection of Ad-SGE-REIC into one side of the tumor induced not only a local antitumor effect but also a bystander abscopal effect in the non-injected tumor, located on the other flank. The number of PD-1+CD8+ T cells increased in both injected and non-injected tumors. PD-1 blockade augmented the local and abscopal antitumor effects of Ad-SGE-REIC by increasing the number of CD8+ T cells in the TME of Egfr-mutant tumors. Depletion of CD8+ cells reverted the antitumor effect, suggesting they contribute to antitumor immunity. Conclusion: Ad-SGE-REIC induced systemic antitumor immunity by modifying the TME status from non-inflamed to inflamed, with infiltration of CD8+ T cells. Additionally, in Egfr-mutant lung cancer, this effect was enhanced by PD-1 blockade. These findings pave the way to establish a novel combined immunotherapy strategy with Ad-SGE-REIC and anti-PD-1 antibody for lung cancer with a non-inflamed TME.
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页码:1 / 10
页数:10
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