CCL21-DC in situ vaccination in murine NSCLC overcomes resistance to immunotherapy and generates systemic tumor-specific immunity

Author:

Salehi-Rad RaminORCID,Lim Raymond J,Du Yushen,Tran Linh M,Li RuiORCID,Ong Stephanie L,Ling Huang Zi,Dumitras Camelia,Zhang Tianhao,Park Stacy J,Crosson William,Kahangi Bitta,Abascal Jensen,Seet Christopher,Oh Michael,Shabihkhani Maryam,Paul ManashORCID,Krysan Kostyantyn,Lisberg Aaron E,Garon Edward BORCID,Liu Bin,Dubinett Steven M

Abstract

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); andKrasG12D(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.

Funder

National Institutes of Health

National Heart, Lung, and Blood Institute

Lung Cancer Foundation of America and International Lung Cancer Foundation Young Investigator Award

Tobacco-Related Disease Research Program Predoctoral Fellowship Award

National Center for Advancing Translational Sciences

Medical Reserach Funds from Department of Veterans Affairs

National Cancer Institute

Publisher

BMJ

Subject

Cancer Research,Pharmacology,Oncology,Molecular Medicine,Immunology,Immunology and Allergy

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