Recruitment of CD103+ dendritic cells via tumor-targeted chemokine delivery enhances efficacy of checkpoint inhibitor immunotherapy

Sci Adv. 2019 Dec 11;5(12):eaay1357. doi: 10.1126/sciadv.aay1357. eCollection 2019 Dec.

Abstract

Although a clinical breakthrough for cancer treatment, it remains that a minority of patients respond to checkpoint inhibitor (CPI) immunotherapy. The composition of tumor-infiltrating immune cells has been identified as a key factor influencing CPI therapy success. Thus, enhancing tumor immune cell infiltration is a critical challenge. A lack of the chemokine CCL4 within the tumor microenvironment leads to the absence of CD103+ dendritic cells (DCs), a crucial cell population influencing CPI responsiveness. Here, we use a tumor stroma-targeting approach to deliver CCL4; by generating a fusion protein of CCL4 and the collagen-binding domain (CBD) of von Willebrand factor, we show that CBD fusion enhances CCL4 tumor localization. Intravenous CBD-CCL4 administration recruits CD103+ DCs and CD8+ T cells and improves the antitumor effect of CPI immunotherapy in multiple tumor models, including poor responders to CPI. Thus, CBD-CCL4 holds clinical translational potential by enhancing efficacy of CPI immunotherapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / genetics
  • Antigens, CD / immunology*
  • CD8-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / pathology
  • Cell Cycle Checkpoints / drug effects
  • Cell Cycle Checkpoints / immunology
  • Chemokine CCL4 / genetics*
  • Chemokine CCL4 / immunology
  • Chemokine CCL4 / pharmacology
  • Collagen / genetics
  • Collagen / immunology
  • Dendritic Cells / drug effects
  • Dendritic Cells / immunology
  • Humans
  • Immunotherapy*
  • Integrin alpha Chains / genetics
  • Integrin alpha Chains / immunology*
  • Lymphocytes, Tumor-Infiltrating / drug effects
  • Lymphocytes, Tumor-Infiltrating / immunology
  • Melanoma / genetics
  • Melanoma / immunology*
  • Melanoma / therapy
  • Melanoma, Experimental / drug therapy
  • Melanoma, Experimental / genetics
  • Melanoma, Experimental / immunology*
  • Melanoma, Experimental / pathology
  • Mice
  • Protein Binding / genetics
  • Tumor Microenvironment / drug effects
  • von Willebrand Factor / genetics

Substances

  • Antigens, CD
  • Chemokine CCL4
  • Integrin alpha Chains
  • alpha E integrins
  • von Willebrand Factor
  • Collagen