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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页数:16
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