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CCL21-DC in situ vaccination in murine NSCLC overcomes resistance to immunotherapy and generates systemic tumor-specific immunity
被引:10
|作者:
Salehi-Rad, Ramin
[1
,2
]
Lim, Raymond J.
[3
]
Du, Yushen
[3
,4
]
Tran, Linh M.
[1
,2
]
Li, Rui
[1
]
Ong, Stephanie L.
[1
]
Ling Huang, Zi
[1
]
Dumitras, Camelia
[1
]
Zhang, Tianhao
[3
]
Park, Stacy J.
[1
]
Crosson, William
[3
]
Kahangi, Bitta
[1
]
Abascal, Jensen
[1
]
Seet, Christopher
[1
]
Oh, Michael
[1
]
Shabihkhani, Maryam
[5
]
Paul, Manash
[1
]
Krysan, Kostyantyn
[1
]
Lisberg, Aaron E.
[1
]
Garon, Edward B.
[1
]
Liu, Bin
[1
]
Dubinett, Steven M.
[1
,2
]
机构:
[1] UCLA, David Geffen Sch Med, Med, Los Angeles, CA 90095 USA
[2] VA Greater Angeles Healthcare Syst, Med, Los Angeles, CA 90073 USA
[3] UCLA, David Geffen Sch Med, Mol & Med Pharmacol, Los Angeles, CA USA
[4] Zhejiang Univ, Sch Med, Med, Hangzhou, Zhejiang, Peoples R China
[5] UCLA, David Geffen Sch Med, Pathol & Lab Med, Los Angeles, CA USA
关键词:
Vaccination;
Non-Small Cell Lung Cancer;
Immunotherapy;
Dendritic Cells;
Tumor Microenvironment;
DENDRITIC CELLS;
LUNG-CANCER;
PD-1;
BLOCKADE;
RESPONSES;
SENSITIVITY;
D O I:
10.1136/jitc-2023-006896
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
BackgroundDespite recent advances in immunotherapy, many patients with non-small cell lung cancer (NSCLC) do not respond to immune checkpoint inhibitors (ICI). Resistance to ICI may be driven by suboptimal priming of antitumor T lymphocytes due to poor antigen presentation as well as their exclusion and impairment by the immunosuppressive tumor microenvironment (TME). In a recent phase I trial in patients with NSCLC, in situ vaccination (ISV) with dendritic cells engineered to secrete CCL21 (CCL21-DC), a chemokine that facilitates the recruitment of T cells and DC, promoted T lymphocyte tumor infiltration and PD-L1 upregulation.MethodsMurine models of NSCLC with distinct driver mutations (KrasG12D/P53+/-/Lkb1-/- (KPL); KrasG12D/P53+/- (KP); and KrasG12D (K)) and varying tumor mutational burden were used to evaluate the efficacy of combination therapy with CCL21-DC ISV plus ICI. Comprehensive analyses of longitudinal preclinical samples by flow cytometry, single cell RNA-sequencing (scRNA-seq) and whole-exome sequencing were performed to assess mechanisms of combination therapy.ResultsISV with CCL21-DC sensitized immune-resistant murine NSCLCs to ICI and led to the establishment of tumor-specific immune memory. Immunophenotyping revealed that CCL21-DC obliterated tumor-promoting neutrophils, promoted sustained infiltration of CD8 cytolytic and CD4 Th1 lymphocytes and enriched progenitor T cells in the TME. Addition of ICI to CCL21-DC further enhanced the expansion and effector function of T cells both locally and systemically. Longitudinal evaluation of tumor mutation profiles revealed that CCL21-DC plus ICI induced immunoediting of tumor subclones, consistent with the broadening of tumor-specific T cell responses.ConclusionsCCL21-DC ISV synergizes with anti-PD-1 to eradicate murine NSCLC. Our data support the clinical application of CCL21-DC ISV in combination with checkpoint inhibition for patients with NSCLC.
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