TY - JOUR
T1 - PD-1 blockade augments CD8+ T cell dependent antitumor immunity triggered by Ad-SGE-REIC in Egfr-mutant lung cancer
AU - Nakasuka, Takamasa
AU - Oohashi, Kadoaki
AU - Nishii, Kazuya
AU - Hirabae, Atsuko
AU - Okawa, Sachi
AU - Tomonobu, Nahoko
AU - Takada, Kenji
AU - Ando, Chihiro
AU - Watanabe, Hiromi
AU - Makimoto, Go
AU - Ninomiya, Kiichiro
AU - Fujii, Masanori
AU - Kubo, Toshio
AU - Ichihara, Eiki
AU - Hotta, Katsuyuki
AU - Tabata, Masahiro
AU - Kumon, Hiromi
AU - Maeda, Yoshinobu
AU - Kiura, Katsuyuki
N1 - Funding Information:
This work was supported by a specific grant from JSPS Grant-in-Aid for Scientific Research [Scientific Research (C): KAKEN 19K08625 to K.O. and K.K.], JSPS Grants-in-Aid for Scientific Research [Scientific Research (B): KAKEN 19H03667 to K.K. and K.O.] and JSPS Grants-in-Aid for Scientific Research [Scientific Research (B): KAKEN 22H03078 to K.O. and K.K.]. This work was also supported by Ryobi Teien Memory Foundation (K.O.), Okayama Medical Foundation (K.O.), Kobayashi Foundation for Cancer Research (K.O.), Takeda Science Foundation (K.O.), Project Mirai Cancer Research Grants (K.O.), Sanyo Broadcasting Foundation (K.O.), and Momotaro-Gene Inc (K.K).
Funding Information:
We are grateful to Ms. Hiromi Nakashima, Ms. Kyoko Maeda from Department of Hematology, Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences. We also thank our laboratory colleagues for the useful discussions. This work was supported by a specific grant from JSPS Grant-in-Aid for Scientific Research [Scientific Research (C): KAKEN 19K08625 to K.O. and K.K.], JSPS Grants-in-Aid for Scientific Research [Scientific Research (B): KAKEN 19H03667 to K.K. and K.O.] and JSPS Grants-in-Aid for Scientific Research [Scientific Research (B): KAKEN 22H03078 to K.O. and K.K.]. This work was also supported by Ryobi Teien Memory Foundation (K.O.), Okayama Medical Foundation (K.O.), Kobayashi Foundation for Cancer Research (K.O.), Takeda Science Foundation (K.O.), Project Mirai Cancer Research Grants (K.O.), Sanyo Broadcasting Foundation (K.O.), and Momotaro-Gene Inc (K.K). The datasets used and/or analyzed during the current study are available from the corresponding author upon reasonable request.
Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2023/4
Y1 - 2023/4
N2 - 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.
AB - 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.
KW - Ad-SGE-REIC
KW - Antitumor immunity
KW - EGFR mutation
KW - Gene therapy
KW - Non-inflamed tumor
KW - Non-small cell lung cancer
KW - PD-1
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U2 - 10.1016/j.lungcan.2023.01.018
DO - 10.1016/j.lungcan.2023.01.018
M3 - Article
C2 - 36753780
AN - SCOPUS:85147457226
SN - 0169-5002
VL - 178
SP - 1
EP - 10
JO - Lung Cancer
JF - Lung Cancer
ER -